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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">biopreparat</journal-id><journal-title-group><journal-title xml:lang="ru">БИОпрепараты. Профилактика, диагностика, лечение</journal-title><trans-title-group xml:lang="en"><trans-title>Biological Products. Prevention, Diagnosis, Treatment</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2221-996X</issn><issn pub-type="epub">2619-1156</issn><publisher><publisher-name>Scientific Centre for Expert Evaluation of Medicinal Products</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.30895/2221-996X-2018-18-2-81-91</article-id><article-id custom-type="elpub" pub-id-type="custom">biopreparat-134</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group></article-categories><title-group><article-title>Адъюванты на основе углеводов для производства вакцин</article-title><trans-title-group xml:lang="en"><trans-title>Carbohydrate-Based Adjuvants for Vaccine Production</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Курашова</surname><given-names>С. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Kurashova</surname><given-names>S. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Младший научный сотрудник</p><p>домовладение 8, стр. 1, поселок Института полиомиелита, поселение Московский, Москва, 108819, Российская Федерация</p></bio><bio xml:lang="en"><p>Junior Researcher</p><p>8/1 housing estate of the Institute of Poliomyelitis, «Moskovsky» settlement, Moscow 108819, Russian Federation</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Дзагурова</surname><given-names>Т. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Dzagurova</surname><given-names>T. K.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Руководитель лаборатории геморрагических лихорадок, д-р мед. наук</p><p>домовладение 8, стр. 1, поселок Института полиомиелита, поселение Московский, Москва, 108819, Российская Федерация</p></bio><bio xml:lang="en"><p>Head of the Laboratory of Hemorrhagic Fevers. Doctor of Medical Sciences</p><p>8/1 housing estate of the Institute of Poliomyelitis, «Moskovsky» settlement, Moscow 108819, Russian Federation</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ишмухаметов</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Ishmukhametov</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Генеральный директор, д-р мед. наук</p><p>домовладение 8, стр. 1, поселок Института полиомиелита, поселение Московский, Москва, 108819, Российская Федерация</p><p>ул. Трубецкая, д. 8, стр. 2, Москва, 119991, Российская Федерация</p></bio><bio xml:lang="en"><p>General Director. Doctor of Medical Sciences</p><p>8/1 housing estate of the Institute of Poliomyelitis, «Moskovsky» settlement, Moscow 108819, Russian Federation</p><p>8/2 Trubetskaya St, Moscow 119991, Russian Federation</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Егорова</surname><given-names>М. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Egorova</surname><given-names>M. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Старший научный сотрудник, канд. биол. наук</p><p>домовладение 8, стр. 1, поселок Института полиомиелита, поселение Московский, Москва, 108819, Российская Федерация</p></bio><bio xml:lang="en"><p>Senior Researcher. Candidate of Biological Sciences</p><p>8/1 housing estate of the Institute of Poliomyelitis, «Moskovsky» settlement, Moscow 108819, Russian Federation</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Баловнева</surname><given-names>М. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Balovneva</surname><given-names>M. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Старший научный сотрудник, канд. биол. наук</p><p>домовладение 8, стр. 1, поселок Института полиомиелита, поселение Московский, Москва, 108819, Российская Федерация</p></bio><bio xml:lang="en"><p>Senior Researcher. Candidate of Biological Sciences</p><p>8/1 housing estate of the Institute of Poliomyelitis, «Moskovsky» settlement, Moscow 108819, Russian Federation</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Соцкова</surname><given-names>С. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Sotskova</surname><given-names>S. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Директор по организационно-методической работе</p><p>домовладение 8, стр. 1, поселок Института полиомиелита, поселение Московский, Москва, 108819, Российская Федерация</p></bio><bio xml:lang="en"><p>Director in Charge of Organisational and Methodical Issues</p><p>8/1 housing estate of the Institute of Poliomyelitis, «Moskovsky» settlement, Moscow 108819, Russian Federation</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ткаченко</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Tkachenko</surname><given-names>E. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Руководитель научного направления, д-р мед. наук, профессор</p><p>домовладение 8, стр. 1, поселок Института полиомиелита, поселение Московский, Москва, 108819, Российская Федерация</p><p>ул. Трубецкая, д. 8, стр. 2, Москва, 119991, Российская Федерация</p></bio><bio xml:lang="en"><p>Scientific Supervisor. Doctor of Medical Sciences, Professor</p><p>8/1 housing estate of the Institute of Poliomyelitis, «Moskovsky» settlement, Moscow 108819, Russian Federation</p><p>8/2 Trubetskaya St, Moscow 119991, Russian Federation</p></bio><email xlink:type="simple">evgeniytkach@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное научное учреждение «Федеральный научный центр исследований и разработки иммунобиологических препаратов им. М.П. Чумакова РАН»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Chumakov Federal Scientific Center for Research and Development of Immune-and-Biological Products of Russian Academy of Sciences</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное научное учреждение «Федеральный научный центр исследований и разработки иммунобиологических препаратов им. М.П. Чумакова РАН»&#13;
&#13;
Федеральное государственное автономное образовательное учреждение высшего образования «Первый Московский государственный медицинский университет имени И.М. Сеченова» Министерства здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Chumakov Federal Scientific Center for Research and Development of Immune-and-Biological Products of Russian Academy of Sciences&#13;
&#13;
Sechenov First Moscow State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>21</day><month>06</month><year>2018</year></pub-date><volume>18</volume><issue>2</issue><fpage>81</fpage><lpage>91</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Курашова С.С., Дзагурова Т.К., Ишмухаметов А.А., Егорова М.С., Баловнева М.В., Соцкова С.Е., Ткаченко Е.А., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Курашова С.С., Дзагурова Т.К., Ишмухаметов А.А., Егорова М.С., Баловнева М.В., Соцкова С.Е., Ткаченко Е.А.</copyright-holder><copyright-holder xml:lang="en">Kurashova S.S., Dzagurova T.K., Ishmukhametov A.A., Egorova M.S., Balovneva M.V., Sotskova S.E., Tkachenko E.A.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.biopreparations.ru/jour/article/view/134">https://www.biopreparations.ru/jour/article/view/134</self-uri><abstract><p>Общепризнанным способом усиления иммуногенности вакцин является добавление в их состав адъювантов. Последние характеризуются большим разнообразием, поэтому подбор  адъюванта осуществляется путем сравнения эффективности адъювантов на моделях  животных, а также оценки их безопасности и переносимости. Среди множества различных  групп веществ, потенциально обладающих адъювантными свойствами, сравнительно мало  внимания уделяют адъювантам на основе углеводов, несмотря на то, что они совместимы с  живыми векторными вакцинами, безопасны, хорошо переносятся, а их производство не  отличается трудоемкостью. Благодаря этим преимуществам применение именно таких  адъювантов в сочетании с любым  типом вакцины, в том числе с векторной или ДНК-вакциной, может быть наиболее  целесообразным и перспективным. В настоящем обзоре рассмотрены различные типы  углеводных адъювантов и механизмы, определяющие их эффективность.</p></abstract><trans-abstract xml:lang="en"><p>Addition of adjuvants is a generally recognized method of enhancing the immunogenicity of vaccines. There is a large variety of  adjuvants, therefore the choice of an adjuvant is based on the  comparison of adjuvants efficacy in animal models, as well as  assessment of their safety and tolerability. There are many different  groups of substances that may have adjuvant properties, but  relatively little attention is paid to carbohydrate-based adjuvants, despite the fact that they are compatible with live vector  vaccines, safe, well tolerated, and their production is not laborious.  Thanks to these advantages the use of these particular adjuvants in  combination with any type of vaccine, including vector vaccines and  DNA vaccines, may be most appropriate and promising. This review  examines various types of carbohydrate adjuvants and the  mechanisms that determine their efficacy. </p></trans-abstract><kwd-group xml:lang="ru"><kwd>адъювант</kwd><kwd>гуморальный иммунитет</kwd><kwd>полисахариды</kwd><kwd>иммуногенность</kwd><kwd>безопасность вакцин</kwd><kwd>живые векторные вакцины</kwd><kwd>иммунитет</kwd><kwd>иммунологическая активность полисахаридов</kwd></kwd-group><kwd-group xml:lang="en"><kwd>adjuvant</kwd><kwd>humoral immunity</kwd><kwd>polysaccharides</kwd><kwd>immunogenicity</kwd><kwd>vaccine safety</kwd><kwd>live vector vaccines</kwd><kwd>immunity</kwd><kwd>immunological activity of polysaccharides</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Дранник ГН. Клиническая иммунология и аллергология. Одесса: АстроПринт; 1999. [Drannik GN. Clinical Immunology and Allergology. Odessa: AstroPrint; 1999 (in Russ.)]</mixed-citation><mixed-citation xml:lang="en">Дранник ГН. Клиническая иммунология и аллергология. Одесса: АстроПринт; 1999. [Drannik GN. Clinical Immunology and Allergology. Odessa: AstroPrint; 1999 (in Russ.)]</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Дитятковская ЕМ, Василевская ИВ, Кийко ЛА. Аллергология и иммунология. Днепропетровск: ФПО ДГМА; 2003. [Dityatkovskaya EM, Vasilevskaya IV, Kijko LА. Allergology and Immunology. Dnepropetrovsk: FPO DGMA; 2003 (in Russ.)]</mixed-citation><mixed-citation xml:lang="en">Дитятковская ЕМ, Василевская ИВ, Кийко ЛА. Аллергология и иммунология. Днепропетровск: ФПО ДГМА; 2003. [Dityatkovskaya EM, Vasilevskaya IV, Kijko LА. Allergology and Immunology. Dnepropetrovsk: FPO DGMA; 2003 (in Russ.)]</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Хаитов РМ. Иммунология: структура и функции иммунной системы: учебное пособие. М.: ГЭОТАР-Медиа; 2013. [Khaitov RM. Immunology: Structure and Functions of the Immune System: Textbook. Moscow: GEOTAR-Media; 2013 (in Russ.)]</mixed-citation><mixed-citation xml:lang="en">Хаитов РМ. Иммунология: структура и функции иммунной системы: учебное пособие. М.: ГЭОТАР-Медиа; 2013. [Khaitov RM. Immunology: Structure and Functions of the Immune System: Textbook. Moscow: GEOTAR-Media; 2013 (in Russ.)]</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Vogel FR. Adjuvants in Perspective. Dev Biol Stand. 1998;92:241–8.</mixed-citation><mixed-citation xml:lang="en">Vogel FR. Adjuvants in Perspective. Dev Biol Stand. 1998;92:241–8.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Vogel FR. Improving Vaccine Performance with Adjuvants. Clin Infect Dis. 2000;30 Suppl 3:S266–70. DOI: 10.1086/313883</mixed-citation><mixed-citation xml:lang="en">Vogel FR. Improving Vaccine Performance with Adjuvants. Clin Infect Dis. 2000;30 Suppl 3:S266–70. DOI: 10.1086/313883</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Исаенко ЕЮ, Бабич ЕМ, Елисеева ИВ, Ждамарова ЛА, Белозерский ВИ, Колпак СА. Адъюванты в современной вакцинологии. Аннали Мечниковського інституту 2013;(4):5– 21. [Isaenko YeYu, Babych YeM, Yelyseyeva IV, Zhdamarova LA, Belozersky VI, Kolpak SA. Adjuvants in Modern Vaccinology. Annali Mechnikovskogo іnstitutu 2013;(4):5–21 (in Russ.)]</mixed-citation><mixed-citation xml:lang="en">Исаенко ЕЮ, Бабич ЕМ, Елисеева ИВ, Ждамарова ЛА, Белозерский ВИ, Колпак СА. Адъюванты в современной вакцинологии. Аннали Мечниковського інституту 2013;(4):5– 21. [Isaenko YeYu, Babych YeM, Yelyseyeva IV, Zhdamarova LA, Belozersky VI, Kolpak SA. Adjuvants in Modern Vaccinology. Annali Mechnikovskogo іnstitutu 2013;(4):5–21 (in Russ.)]</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Gupta RK, Siber GR. Adjuvants for Human Vaccines — Current Status, Problems and Future Prospects. Vaccine 1995;13(14):1263–76. DOI: 10.1016/0264-410X(95)00011-O</mixed-citation><mixed-citation xml:lang="en">Gupta RK, Siber GR. Adjuvants for Human Vaccines — Current Status, Problems and Future Prospects. Vaccine 1995;13(14):1263–76. DOI: 10.1016/0264-410X(95)00011-O</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">O’Hagan DT, ed. Vaccine Adjuvants: Preparation Methods and Research Protocols. Totowa NJ: Humana Press; 2000.</mixed-citation><mixed-citation xml:lang="en">O’Hagan DT, ed. Vaccine Adjuvants: Preparation Methods and Research Protocols. Totowa NJ: Humana Press; 2000.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Козлов ВГ, Ожерелков СВ, Санин АВ, Кожевникова ТН. Адъюванты в современной медицине и ветеринарии. Журнал микробиологии, эпидемиологии и иммунобиологии 2014;(1):91–102. [Kozlov VG, Ozherelkov SV, Sanin AV, Kozhevnikova TN. Adjuvants in Modern Medicine and Veterinary. Zhurnal mikrobiologii, epidemiologii, i immunobiologii 2014;(1):91– 102 (in Russ.)]</mixed-citation><mixed-citation xml:lang="en">Козлов ВГ, Ожерелков СВ, Санин АВ, Кожевникова ТН. Адъюванты в современной медицине и ветеринарии. Журнал микробиологии, эпидемиологии и иммунобиологии 2014;(1):91–102. [Kozlov VG, Ozherelkov SV, Sanin AV, Kozhevnikova TN. Adjuvants in Modern Medicine and Veterinary. Zhurnal mikrobiologii, epidemiologii, i immunobiologii 2014;(1):91– 102 (in Russ.)]</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Суворов АН, Леонтьева ГФ, Мерингова ЛФ, Грабовская КБ, Гупалова ТВ, Воробьева ЕИ и др. Влияние различных адъювантов на иммуногенность компонентов вакцины против стрептококков группы B. Медицинская Иммунология 2008;10(2-3):215–22. [Suvorov AN, Leontyeva GF, Meringova LF, Grabovskaya KB, Gupalova TV, Vorobyeva EI, et al. Effects of Different Adjuvants upon Immunogenicity of Anti-Group B Streptococcal Vaccine Components. Medicinskaya Immunologiya 2008;10(2-3):215–22 (in Russ.)]</mixed-citation><mixed-citation xml:lang="en">Суворов АН, Леонтьева ГФ, Мерингова ЛФ, Грабовская КБ, Гупалова ТВ, Воробьева ЕИ и др. Влияние различных адъювантов на иммуногенность компонентов вакцины против стрептококков группы B. Медицинская Иммунология 2008;10(2-3):215–22. [Suvorov AN, Leontyeva GF, Meringova LF, Grabovskaya KB, Gupalova TV, Vorobyeva EI, et al. Effects of Different Adjuvants upon Immunogenicity of Anti-Group B Streptococcal Vaccine Components. Medicinskaya Immunologiya 2008;10(2-3):215–22 (in Russ.)]</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Aguilar JC, Rodriguez EG. Vaccine Adjuvants Revisited. Vaccine 2007;25(19):3752–62. DOI: 10.1016/j.vaccine.2007.01.111</mixed-citation><mixed-citation xml:lang="en">Aguilar JC, Rodriguez EG. Vaccine Adjuvants Revisited. Vaccine 2007;25(19):3752–62. DOI: 10.1016/j.vaccine.2007.01.111</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">McKee AS, Marrack P. Old and New Adjuvants. Curr Opin Immunol. 2017;47:44–51. DOI: 10.1016/j.coi.2017.06.005</mixed-citation><mixed-citation xml:lang="en">McKee AS, Marrack P. Old and New Adjuvants. Curr Opin Immunol. 2017;47:44–51. DOI: 10.1016/j.coi.2017.06.005</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Savelkoul HF, Ferro VA, Strioga MM, Schijns VE. Choice and Design of Adjuvants for Parenteral and Mucosal Vaccines. Vaccines (Basel) 2015;3(1):148–71. DOI: 10.3390/vaccines3010148</mixed-citation><mixed-citation xml:lang="en">Savelkoul HF, Ferro VA, Strioga MM, Schijns VE. Choice and Design of Adjuvants for Parenteral and Mucosal Vaccines. Vaccines (Basel) 2015;3(1):148–71. DOI: 10.3390/vaccines3010148</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Petrovsky N, Larena M, Siddharthan V, Prow NA, Hall RA, Lobigs M, Morrey J. An Inactivated Cell Culture Japanese Encephalitis Vaccine (JE-ADVAX) Formulated with Delta Inulin Adjuvant Provides Robust Heterologous Protection Against West Nile Encephalitis via Cross-Protective Memory B Cells and Neutralizing Antibody. J Virol. 2013;87(18):10324–33. DOI: 10.1128/JVI.00480-13</mixed-citation><mixed-citation xml:lang="en">Petrovsky N, Larena M, Siddharthan V, Prow NA, Hall RA, Lobigs M, Morrey J. An Inactivated Cell Culture Japanese Encephalitis Vaccine (JE-ADVAX) Formulated with Delta Inulin Adjuvant Provides Robust Heterologous Protection Against West Nile Encephalitis via Cross-Protective Memory B Cells and Neutralizing Antibody. J Virol. 2013;87(18):10324–33. DOI: 10.1128/JVI.00480-13</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Passeri E, Villa C, Couette M, Itti E, Brugieres P, Cesaro P, et al. Long-Term Follow-up of Cognitive Dysfunction in Patients with Aluminum Hydroxide-Induced Macrophagic Myofasciitis (MMF). J Inorg Biochem. 2011;105(11):1457–63. DOI: 10.1016/j.jinorgbio.2011.08.006</mixed-citation><mixed-citation xml:lang="en">Passeri E, Villa C, Couette M, Itti E, Brugieres P, Cesaro P, et al. Long-Term Follow-up of Cognitive Dysfunction in Patients with Aluminum Hydroxide-Induced Macrophagic Myofasciitis (MMF). J Inorg Biochem. 2011;105(11):1457–63. DOI: 10.1016/j.jinorgbio.2011.08.006</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Ciabattini A, Pettini E, Fiorino F, Pastore G, Andersen P, Pozzi G, Medaglini D. Modulation of Primary Immune Response by Different Vaccine Adjuvants. Front Immunol. 2016;7:427. DOI: 10.3389/fimmu.2016.00427</mixed-citation><mixed-citation xml:lang="en">Ciabattini A, Pettini E, Fiorino F, Pastore G, Andersen P, Pozzi G, Medaglini D. Modulation of Primary Immune Response by Different Vaccine Adjuvants. Front Immunol. 2016;7:427. DOI: 10.3389/fimmu.2016.00427</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Petrovsky N. Comparative Safety of Vaccine Adjuvants: A Summary of Current Evidence and Future Needs. Drug Saf. 2015;38(11):1059–74. DOI: 10.1007/s40264-015-0350-4</mixed-citation><mixed-citation xml:lang="en">Petrovsky N. Comparative Safety of Vaccine Adjuvants: A Summary of Current Evidence and Future Needs. Drug Saf. 2015;38(11):1059–74. DOI: 10.1007/s40264-015-0350-4</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Cooper PD, Carter M. Anti-Complementary Action of Polymorphic «Solubility Forms» of Particulate Inulin. Mol Immunol. 1986;23(8):895–901.</mixed-citation><mixed-citation xml:lang="en">Cooper PD, Carter M. Anti-Complementary Action of Polymorphic «Solubility Forms» of Particulate Inulin. Mol Immunol. 1986;23(8):895–901.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Cooper PD, Barclay TG, Ginic-Markovic M, Petrovsky N. The Polysaccharide Inulin is Characterized by an Extensive Series of Periodic Isoforms with Varying Biological Actions. Glycobiology 2013;23(10):1164–74. DOI: 10.1093/glycob/cwt053</mixed-citation><mixed-citation xml:lang="en">Cooper PD, Barclay TG, Ginic-Markovic M, Petrovsky N. The Polysaccharide Inulin is Characterized by an Extensive Series of Periodic Isoforms with Varying Biological Actions. Glycobiology 2013;23(10):1164–74. DOI: 10.1093/glycob/cwt053</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Cooper PD, Petrovsky N. Delta Inulin: A Novel, Immunologically Active, Stable Packing Structure Comprising β-D-[2 → 1] poly(fructo-furanosyl) α-D-glucose Polymers. Glycobiology 2011;21(5):595–606. DOI: 10.1093/glycob/cwq201</mixed-citation><mixed-citation xml:lang="en">Cooper PD, Petrovsky N. Delta Inulin: A Novel, Immunologically Active, Stable Packing Structure Comprising β-D-[2 → 1] poly(fructo-furanosyl) α-D-glucose Polymers. Glycobiology 2011;21(5):595–606. DOI: 10.1093/glycob/cwq201</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Honda-Okubo Y, Saade F, Petrovsky N. Advax™, a Polysaccharide Adjuvant Derived from Delta Inulin, Provides Improved Influenza Vaccine Protection through Broad-Based Enhancement of Adaptive Immune Responses. Vaccine 2012;30(36):5373–81. DOI: 10.1016/j.vaccine.2012.06.021</mixed-citation><mixed-citation xml:lang="en">Honda-Okubo Y, Saade F, Petrovsky N. Advax™, a Polysaccharide Adjuvant Derived from Delta Inulin, Provides Improved Influenza Vaccine Protection through Broad-Based Enhancement of Adaptive Immune Responses. Vaccine 2012;30(36):5373–81. DOI: 10.1016/j.vaccine.2012.06.021</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Larena M, Prow NA, Hall RA, Petrovsky N, Lobigs M. JEADVAX Vaccine Protection against Japanese Encephalitis Virus Mediated by Memory B Cells in the Absence of CD8(+) T Cells and Pre-Exposure Neutralizing Antibody. J Virol. 2013;87(8):4395–402. DOI: 10.1128/JVI.03144-12</mixed-citation><mixed-citation xml:lang="en">Larena M, Prow NA, Hall RA, Petrovsky N, Lobigs M. JEADVAX Vaccine Protection against Japanese Encephalitis Virus Mediated by Memory B Cells in the Absence of CD8(+) T Cells and Pre-Exposure Neutralizing Antibody. J Virol. 2013;87(8):4395–402. DOI: 10.1128/JVI.03144-12</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Saade F, Honda-Okubo Y, Trec S, Petrovsky N. A Novel Hepatitis B Vaccine Containing Advax™, a Polysaccharide Adjuvant Derived from Delta Inulin, Induces Robust Humoral and Cellular Immunity with Minimal Reactogenicity in Preclinical Testing. Vaccine 2013;31(15):1999– 2007. DOI: 10.1016/j.vaccine.2012.12.077</mixed-citation><mixed-citation xml:lang="en">Saade F, Honda-Okubo Y, Trec S, Petrovsky N. A Novel Hepatitis B Vaccine Containing Advax™, a Polysaccharide Adjuvant Derived from Delta Inulin, Induces Robust Humoral and Cellular Immunity with Minimal Reactogenicity in Preclinical Testing. Vaccine 2013;31(15):1999– 2007. DOI: 10.1016/j.vaccine.2012.12.077</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Cristillo AD, Ferrari MG, Hudacik L, Lewis B, Galmin L, Bowen B, et al. Induction of Mucosal and Systemic Antibody and T-cell Responses Following Prime-Boost Immunization with Novel Adjuvanted Human Immunodeficiency Virus-1-vaccine Formulations. J Gen Virol. 2011;92(Pt 1):128–40. DOI: 10.1099/vir.0.023242-0</mixed-citation><mixed-citation xml:lang="en">Cristillo AD, Ferrari MG, Hudacik L, Lewis B, Galmin L, Bowen B, et al. Induction of Mucosal and Systemic Antibody and T-cell Responses Following Prime-Boost Immunization with Novel Adjuvanted Human Immunodeficiency Virus-1-vaccine Formulations. J Gen Virol. 2011;92(Pt 1):128–40. DOI: 10.1099/vir.0.023242-0</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Layton RC, Petrovsky N, Gigliotti AP, Pollock Z, Knight J, Donart N, et al. Delta Inulin Polysaccharide Adjuvant Enhances the Ability of Split-Virion H5N1 Vaccine to Protect against Lethal Challenge in Ferrets. Vaccine 2011;29(37):6242–51. DOI: 10.1016/j.vaccine.2011.06.078</mixed-citation><mixed-citation xml:lang="en">Layton RC, Petrovsky N, Gigliotti AP, Pollock Z, Knight J, Donart N, et al. Delta Inulin Polysaccharide Adjuvant Enhances the Ability of Split-Virion H5N1 Vaccine to Protect against Lethal Challenge in Ferrets. Vaccine 2011;29(37):6242–51. DOI: 10.1016/j.vaccine.2011.06.078</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Lobigs M, Pavy M, Hall RA, Lobigs P, Cooper P, Komiya T, et al. An Inactivated Vero Cell- Grown Japanese Encephalitis Vaccine Formulated with Advax, a Novel Inulin-Based Adjuvant, Induces Protective Neutralizing Antibody against Homologous and Heterologous Flaviviruses. J Gen Virol. 2010;91(Pt 6):1407–17. DOI: 10.1099/vir.0.019190-0</mixed-citation><mixed-citation xml:lang="en">Lobigs M, Pavy M, Hall RA, Lobigs P, Cooper P, Komiya T, et al. An Inactivated Vero Cell- Grown Japanese Encephalitis Vaccine Formulated with Advax, a Novel Inulin-Based Adjuvant, Induces Protective Neutralizing Antibody against Homologous and Heterologous Flaviviruses. J Gen Virol. 2010;91(Pt 6):1407–17. DOI: 10.1099/vir.0.019190-0</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Eckersley AM, Petrovsky N, Kinne J, Wernery R, Wernery U. Improving the Dromedary Antibody Response: the Hunt for the Ideal Camel Adjuvant. J Camel Pract Res. 2011;18(1):35–46.</mixed-citation><mixed-citation xml:lang="en">Eckersley AM, Petrovsky N, Kinne J, Wernery R, Wernery U. Improving the Dromedary Antibody Response: the Hunt for the Ideal Camel Adjuvant. J Camel Pract Res. 2011;18(1):35–46.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Gordon DL, Sajkov D, Woodman RJ, Honda-Okubo Y, Cox MM, Heinzel S, Petrovsky N. Randomized Clinical Trial of Immunogenicity and Safety of a Recombinant H1N1/2009 Pandemic Influenza Vaccine Containing Advax™ Polysaccharide Adjuvant. Vaccine 2012;30(36):5407–16. DOI: 10.1016/j.vaccine.2012.06.009</mixed-citation><mixed-citation xml:lang="en">Gordon DL, Sajkov D, Woodman RJ, Honda-Okubo Y, Cox MM, Heinzel S, Petrovsky N. Randomized Clinical Trial of Immunogenicity and Safety of a Recombinant H1N1/2009 Pandemic Influenza Vaccine Containing Advax™ Polysaccharide Adjuvant. Vaccine 2012;30(36):5407–16. DOI: 10.1016/j.vaccine.2012.06.009</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Houston WE, Crabbs CL, Kremer RJ, Springer JW. Adjuvant Effects of Diethylaminoethyl- dextran. Infect Immun. 1976;13(6):1559–62.</mixed-citation><mixed-citation xml:lang="en">Houston WE, Crabbs CL, Kremer RJ, Springer JW. Adjuvant Effects of Diethylaminoethyl- dextran. Infect Immun. 1976;13(6):1559–62.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Kaistha J, Sokhey J, Singh S, Kumar S, John PC, Sharma NC. Adjuvant Effect of DEAE- dextran and Tetanus Toxoid on Whole Cell Heat Inactivated Phenol Preserved Typhoid Vaccine. Indian J Pathol Microbiol. 1996;39(4):287–92.</mixed-citation><mixed-citation xml:lang="en">Kaistha J, Sokhey J, Singh S, Kumar S, John PC, Sharma NC. Adjuvant Effect of DEAE- dextran and Tetanus Toxoid on Whole Cell Heat Inactivated Phenol Preserved Typhoid Vaccine. Indian J Pathol Microbiol. 1996;39(4):287–92.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Bachelder EM, Beaudette TT, Broaders KE, Frechet JM, Albrecht MT, Mateczun AJ, et al. In vitro Analysis of Acetalated Dextran Microparticles as a Potent Delivery Platform for Vaccine Adjuvants. Mol Pharm. 2010;7(3):826–35. DOI: 10.1021/mp900311x</mixed-citation><mixed-citation xml:lang="en">Bachelder EM, Beaudette TT, Broaders KE, Frechet JM, Albrecht MT, Mateczun AJ, et al. In vitro Analysis of Acetalated Dextran Microparticles as a Potent Delivery Platform for Vaccine Adjuvants. Mol Pharm. 2010;7(3):826–35. DOI: 10.1021/mp900311x</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Schorlemmer HU, Bitter-Suermann D, Allison AC. Complement Activation by the Alternative Pathway and Macrophage Enzyme Secretion in the Pathogenesis of Chronic Inflammation. Immunology 1977;32(6):929–40.</mixed-citation><mixed-citation xml:lang="en">Schorlemmer HU, Bitter-Suermann D, Allison AC. Complement Activation by the Alternative Pathway and Macrophage Enzyme Secretion in the Pathogenesis of Chronic Inflammation. Immunology 1977;32(6):929–40.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Lamkanfi M, Malireddi RK, Kanneganti TD. Fungal Zymosan and Mannan Activate the Cryopyrin Inflammasome. J Biol Chem. 2009;284(31):20574–81. DOI: 10.1074/jbc.M109.023689</mixed-citation><mixed-citation xml:lang="en">Lamkanfi M, Malireddi RK, Kanneganti TD. Fungal Zymosan and Mannan Activate the Cryopyrin Inflammasome. J Biol Chem. 2009;284(31):20574–81. DOI: 10.1074/jbc.M109.023689</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Morikawa K, Takeda R, Yamazaki M, Mizuno D. Induction of Tumoricidal Activity of Polymorphonuclear Leukocytes by a Linear beta-1,3-D-glucan and Other Immunomodulators in Murine Cells. Cancer Res. 1985;45(4):1496–501.</mixed-citation><mixed-citation xml:lang="en">Morikawa K, Takeda R, Yamazaki M, Mizuno D. Induction of Tumoricidal Activity of Polymorphonuclear Leukocytes by a Linear beta-1,3-D-glucan and Other Immunomodulators in Murine Cells. Cancer Res. 1985;45(4):1496–501.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Ara Y, Saito T, Takagi T, Hagiwara E, Miyagi Y, Sugiyama M, et al. Zymosan Enhances the Immune Response to DNA Vaccine for Human Immunodeficiency Virus Type-1 through the Activation of Complement System. Immunology 2001;103(1):98–105.</mixed-citation><mixed-citation xml:lang="en">Ara Y, Saito T, Takagi T, Hagiwara E, Miyagi Y, Sugiyama M, et al. Zymosan Enhances the Immune Response to DNA Vaccine for Human Immunodeficiency Virus Type-1 through the Activation of Complement System. Immunology 2001;103(1):98–105.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Jeannin JF, Lagadec P, Pelletier H, Reisser D, Olsson NO, Chihara G, Martin F. Regression Induced by Lentinan, of Peritoneal Carcinomatoses in a Model of Colon Cancer in Rat. Int J Immunopharmacol. 1988;10(7):855–61.</mixed-citation><mixed-citation xml:lang="en">Jeannin JF, Lagadec P, Pelletier H, Reisser D, Olsson NO, Chihara G, Martin F. Regression Induced by Lentinan, of Peritoneal Carcinomatoses in a Model of Colon Cancer in Rat. Int J Immunopharmacol. 1988;10(7):855–61.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Wang J, Zhou ZD, Xia DJ. Study on Effect of Lentinan in Enhancing Anti-Tumor Action of Dendritic Cytoma Vaccine and Its Mechanism. Zhongguo Zhong Xi Yi Jie He Za Zhi. 2007;27(1):60–4.</mixed-citation><mixed-citation xml:lang="en">Wang J, Zhou ZD, Xia DJ. Study on Effect of Lentinan in Enhancing Anti-Tumor Action of Dendritic Cytoma Vaccine and Its Mechanism. Zhongguo Zhong Xi Yi Jie He Za Zhi. 2007;27(1):60–4.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Guo Z, Hu Y, Wang D, Ma X, Zhao X, Zhao B, et al. Sulfated Modification Can Enhance the Adjuvanticity of Lentinan and Improve the Immune Effect of ND Vaccine. Vaccine 2009;27(5):660–5. DOI: 10.1016/j.vaccine.2008.11.038</mixed-citation><mixed-citation xml:lang="en">Guo Z, Hu Y, Wang D, Ma X, Zhao X, Zhao B, et al. Sulfated Modification Can Enhance the Adjuvanticity of Lentinan and Improve the Immune Effect of ND Vaccine. Vaccine 2009;27(5):660–5. DOI: 10.1016/j.vaccine.2008.11.038</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Mohagheghpour N, Dawson M, Hobbs P, Judd A, Winant R, Dousman L, et al. Glucans as Immunological Adjuvants. Adv Exp Med Biol. 1995;383:13–22.</mixed-citation><mixed-citation xml:lang="en">Mohagheghpour N, Dawson M, Hobbs P, Judd A, Winant R, Dousman L, et al. Glucans as Immunological Adjuvants. Adv Exp Med Biol. 1995;383:13–22.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Huang H, Ostroff GR, Lee CK, Specht CA, Levitz SM. Robust Stimulation of Humoral and Cellular Immune Responses Following Vaccination with Antigen-Loaded Beta-Glucan Particles. MBio. 2010;1(3):e00164–10. DOI: 10.1128/mBio.00164-10</mixed-citation><mixed-citation xml:lang="en">Huang H, Ostroff GR, Lee CK, Specht CA, Levitz SM. Robust Stimulation of Humoral and Cellular Immune Responses Following Vaccination with Antigen-Loaded Beta-Glucan Particles. MBio. 2010;1(3):e00164–10. DOI: 10.1128/mBio.00164-10</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Takahara K, Yashima Y, Omatsu Y, Yoshida H, Kimura Y, Kang YS, et al. Functional Comparison of the Mouse DCSIGN, SIGNR1, SIGNR3 and Langerin, C-type Lectins. Int Immunol. 2004;16(6):819–29. DOI: 10.1093/intimm/dxh084</mixed-citation><mixed-citation xml:lang="en">Takahara K, Yashima Y, Omatsu Y, Yoshida H, Kimura Y, Kang YS, et al. Functional Comparison of the Mouse DCSIGN, SIGNR1, SIGNR3 and Langerin, C-type Lectins. Int Immunol. 2004;16(6):819–29. DOI: 10.1093/intimm/dxh084</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Sheng KC, Pouniotis DS, Wright MD, Tang CK, Lazoura E, Pietersz GA, Apostolopoulos V. Mannan Derivatives Induce Phenotypic and Functional Maturation of Mouse Dendritic Cells. Immunology 2006;118(3):372–83. DOI: 10.1111/j.1365-2567.2006.02384.x</mixed-citation><mixed-citation xml:lang="en">Sheng KC, Pouniotis DS, Wright MD, Tang CK, Lazoura E, Pietersz GA, Apostolopoulos V. Mannan Derivatives Induce Phenotypic and Functional Maturation of Mouse Dendritic Cells. Immunology 2006;118(3):372–83. DOI: 10.1111/j.1365-2567.2006.02384.x</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Vassilaros S, Tsibanis A, Tsikkinis A, Pietersz GA, McKenzie IF, Apostolopoulos V. Up to 15- year Clinical Follow-up of a Pilot Phase III Immunotherapy Study in Stage II Breast Cancer Patients using Oxidized Mannan- MUC1. Immunotherapy 2013;5(11):1177–82. DOI: 10.2217/imt.13.126</mixed-citation><mixed-citation xml:lang="en">Vassilaros S, Tsibanis A, Tsikkinis A, Pietersz GA, McKenzie IF, Apostolopoulos V. Up to 15- year Clinical Follow-up of a Pilot Phase III Immunotherapy Study in Stage II Breast Cancer Patients using Oxidized Mannan- MUC1. Immunotherapy 2013;5(11):1177–82. DOI: 10.2217/imt.13.126</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Katsara M, Yuriev E, Ramsland PA, Tselios T, Deraos G, Lourbopoulos A, et al. Altered Peptide Ligands of Myelin Basic Protein (MBP87-99) Conjugated to Reduced Mannan Modulate Immune Responses in Mice. Immunology 2009;128(4):521–33. DOI: 10.1111/j.1365-2567.2009.03137.x</mixed-citation><mixed-citation xml:lang="en">Katsara M, Yuriev E, Ramsland PA, Tselios T, Deraos G, Lourbopoulos A, et al. Altered Peptide Ligands of Myelin Basic Protein (MBP87-99) Conjugated to Reduced Mannan Modulate Immune Responses in Mice. Immunology 2009;128(4):521–33. DOI: 10.1111/j.1365-2567.2009.03137.x</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Petrushina I, Ghochikyan A, Mkrtichyan M, Mamikonyan G, Movsesyan N, Ajdari R, et al. Mannan-Abeta28 Conjugate Prevents Abeta-plaque Deposition, but Increases Microhemor- rhages in the Brains of Vaccinated Tg2576 (APPsw) Mice. J Neuroinflammation. 2008;5:42. DOI: 10.1186/1742-2094-5-42</mixed-citation><mixed-citation xml:lang="en">Petrushina I, Ghochikyan A, Mkrtichyan M, Mamikonyan G, Movsesyan N, Ajdari R, et al. Mannan-Abeta28 Conjugate Prevents Abeta-plaque Deposition, but Increases Microhemor- rhages in the Brains of Vaccinated Tg2576 (APPsw) Mice. J Neuroinflammation. 2008;5:42. DOI: 10.1186/1742-2094-5-42</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Kawakami S, Sato A, Nishikawa M, Yamashita F, Hashida M. Mannose Receptor-Mediated Gene Transfer into Macrophages using Novel Mannosylated Cationic Liposomes. Gene Ther. 2000;7(4):292–9. DOI: 10.1038/sj.gt.3301089</mixed-citation><mixed-citation xml:lang="en">Kawakami S, Sato A, Nishikawa M, Yamashita F, Hashida M. Mannose Receptor-Mediated Gene Transfer into Macrophages using Novel Mannosylated Cationic Liposomes. Gene Ther. 2000;7(4):292–9. DOI: 10.1038/sj.gt.3301089</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Lu Y, Kawakami S, Yamashita F, Hashida M. Development of an Antigen-Presenting Cell- Targeted DNA Vaccine Against Melanoma by Mannosylated Liposomes. Biomaterials 2007;28(21):3255–62. DOI: 10.1016/j.biomaterials.2007.03.028</mixed-citation><mixed-citation xml:lang="en">Lu Y, Kawakami S, Yamashita F, Hashida M. Development of an Antigen-Presenting Cell- Targeted DNA Vaccine Against Melanoma by Mannosylated Liposomes. Biomaterials 2007;28(21):3255–62. DOI: 10.1016/j.biomaterials.2007.03.028</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao Z, Yao Y, Ding Z, Chen X, Xie K, Luo Y, et al. Antitumour Immunity Mediated by Mannan-Modified Adenovirus Vectors Expressing VE-cadherin. Vaccine 2011;29(25):4218–24. DOI: 10.1016/j.vaccine.2011.03.109</mixed-citation><mixed-citation xml:lang="en">Zhao Z, Yao Y, Ding Z, Chen X, Xie K, Luo Y, et al. Antitumour Immunity Mediated by Mannan-Modified Adenovirus Vectors Expressing VE-cadherin. Vaccine 2011;29(25):4218–24. DOI: 10.1016/j.vaccine.2011.03.109</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Arca HC, Gunbeyaz M, Senel S. Chitosan-based Systems for the Delivery of Vaccine Antigens. Expert Rev Vaccines 2009;8(7):937–53. DOI: 10.1586/erv.09.47</mixed-citation><mixed-citation xml:lang="en">Arca HC, Gunbeyaz M, Senel S. Chitosan-based Systems for the Delivery of Vaccine Antigens. Expert Rev Vaccines 2009;8(7):937–53. DOI: 10.1586/erv.09.47</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Ghendon Y, Markushin S, Vasiliev Y, Akopova I, Koptiaeva I, Krivtsov G, et al. Evaluation of Properties of Chitosan as an Adjuvant for Inactivated Influenza Vaccines Administered Parenterally. J Med Virol. 2009;81(3):494–506. DOI: 10.1002/jmv.21415</mixed-citation><mixed-citation xml:lang="en">Ghendon Y, Markushin S, Vasiliev Y, Akopova I, Koptiaeva I, Krivtsov G, et al. Evaluation of Properties of Chitosan as an Adjuvant for Inactivated Influenza Vaccines Administered Parenterally. J Med Virol. 2009;81(3):494–506. DOI: 10.1002/jmv.21415</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Chang H, Li X, Teng Y, Liang Y, Peng B, Fang F, Chen Z. Comparison of Adjuvant Efficacy of Chitosan and Aluminum Hydroxide for Intraperitoneally Administered Inactivated Influenza H5N1 Vaccine. DNA Cell Biol. 2010;29(9):563–8. DOI: 10.1089/dna.2009.0977</mixed-citation><mixed-citation xml:lang="en">Chang H, Li X, Teng Y, Liang Y, Peng B, Fang F, Chen Z. Comparison of Adjuvant Efficacy of Chitosan and Aluminum Hydroxide for Intraperitoneally Administered Inactivated Influenza H5N1 Vaccine. DNA Cell Biol. 2010;29(9):563–8. DOI: 10.1089/dna.2009.0977</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Kotze AF, Luessen HL, de Leeuw BJ, de Boer BG, Verhoef JC, Junginger HE. N-trimethyl Chitosan Chloride as a Potential Absorption Enhancer Across Mucosal Surfaces: In Vitro Evaluation in Intestinal Epithelial Cells (Caco-2). Pharm Res. 1997;14(9):1197–202.</mixed-citation><mixed-citation xml:lang="en">Kotze AF, Luessen HL, de Leeuw BJ, de Boer BG, Verhoef JC, Junginger HE. N-trimethyl Chitosan Chloride as a Potential Absorption Enhancer Across Mucosal Surfaces: In Vitro Evaluation in Intestinal Epithelial Cells (Caco-2). Pharm Res. 1997;14(9):1197–202.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Baudner BC, Giuliani MM, Verhoef JC, Rappuoli R, Junginger HE, Giudice GD. The Concomitant Use of the LTK63 Mucosal Adjuvant and of Chitosan-Based Delivery System Enhances the Immunogenicity and Efficacy of Intranasally Administered Vaccines. Vaccine 2003;21(25– 26):3837–44.</mixed-citation><mixed-citation xml:lang="en">Baudner BC, Giuliani MM, Verhoef JC, Rappuoli R, Junginger HE, Giudice GD. The Concomitant Use of the LTK63 Mucosal Adjuvant and of Chitosan-Based Delivery System Enhances the Immunogenicity and Efficacy of Intranasally Administered Vaccines. Vaccine 2003;21(25– 26):3837–44.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Khatri K, Goyal AK, Gupta PN, Mishra N, Vyas SP. Plasmid DNA Loaded Chitosan Nanoparticles for Nasal Mucosal Immunization Against Hepatitis B. Int J Pharm. 2008;354(1– 2):235–41. DOI: 10.1016/j.ijpharm.2007.11.027</mixed-citation><mixed-citation xml:lang="en">Khatri K, Goyal AK, Gupta PN, Mishra N, Vyas SP. Plasmid DNA Loaded Chitosan Nanoparticles for Nasal Mucosal Immunization Against Hepatitis B. Int J Pharm. 2008;354(1– 2):235–41. DOI: 10.1016/j.ijpharm.2007.11.027</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Gogev S, de Fays K, Versali MF, Gautier S, Thiry E. Glycol Chitosan Improves the Efficacy of Intranasally Administrated Replication Defective Human Adenovirus Type 5 Expressing Glycoprotein D of Bovine Herpesvirus 1. Vaccine 2004;22(15– 16):1946–53. DOI: 10.1016/j.vaccine.2003.11.011</mixed-citation><mixed-citation xml:lang="en">Gogev S, de Fays K, Versali MF, Gautier S, Thiry E. Glycol Chitosan Improves the Efficacy of Intranasally Administrated Replication Defective Human Adenovirus Type 5 Expressing Glycoprotein D of Bovine Herpesvirus 1. Vaccine 2004;22(15– 16):1946–53. DOI: 10.1016/j.vaccine.2003.11.011</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Rauw F, Gardin Y, Palya V, Anbari S, Lemaire S, Boschmans M, et al. Improved Vaccination Against Newcastle Disease by an in Ovo Recombinant HVT-ND Combined with an Adjuvanted Live Vaccine at Day-Old. Vaccine 2010;28(3):823–33. DOI: 10.1016/j.vaccine.2009.10.049</mixed-citation><mixed-citation xml:lang="en">Rauw F, Gardin Y, Palya V, Anbari S, Lemaire S, Boschmans M, et al. Improved Vaccination Against Newcastle Disease by an in Ovo Recombinant HVT-ND Combined with an Adjuvanted Live Vaccine at Day-Old. Vaccine 2010;28(3):823–33. DOI: 10.1016/j.vaccine.2009.10.049</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Wang X, Zhang W, Liu F, Zheng M, Zheng D, Zhang T, et al. Intranasal Immunization with Live Attenuated Influenza Vaccine Plus Chitosan as an Adjuvant Protects Mice against Homologous and Heterologous Virus Challenge. Arch Virol. 2012;157(8):1451–61. DOI: 10.1007/s00705-012-1318-7</mixed-citation><mixed-citation xml:lang="en">Wang X, Zhang W, Liu F, Zheng M, Zheng D, Zhang T, et al. Intranasal Immunization with Live Attenuated Influenza Vaccine Plus Chitosan as an Adjuvant Protects Mice against Homologous and Heterologous Virus Challenge. Arch Virol. 2012;157(8):1451–61. DOI: 10.1007/s00705-012-1318-7</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">El-Kamary SS, Pasetti MF, Mendelman PM, Frey SE, Bernstein DI, Treanor JJ, et al. Adjuvanted Intranasal Norwalk Virus-Like Particle Vaccine Elicits Antibodies and Antibody- Secreting Cells that Express Homing Receptors for Mucosal and Peripheral Lymphoid Tissues. J Infect Dis. 2010;202(11):1649–58. DOI: 10.1086/657087</mixed-citation><mixed-citation xml:lang="en">El-Kamary SS, Pasetti MF, Mendelman PM, Frey SE, Bernstein DI, Treanor JJ, et al. Adjuvanted Intranasal Norwalk Virus-Like Particle Vaccine Elicits Antibodies and Antibody- Secreting Cells that Express Homing Receptors for Mucosal and Peripheral Lymphoid Tissues. J Infect Dis. 2010;202(11):1649–58. DOI: 10.1086/657087</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Lemke CD, Graham JB, Geary SM, Zamba G, Lubaroff DM, Salem AK. Chitosan is a Surprising Negative Modulator of Cytotoxic CD8+ T Cell Responses Elicited by Adenovirus Cancer Vaccines. Mol Pharm. 2011;8(5):1652–61. DOI: 10.1021/mp100464y</mixed-citation><mixed-citation xml:lang="en">Lemke CD, Graham JB, Geary SM, Zamba G, Lubaroff DM, Salem AK. Chitosan is a Surprising Negative Modulator of Cytotoxic CD8+ T Cell Responses Elicited by Adenovirus Cancer Vaccines. Mol Pharm. 2011;8(5):1652–61. DOI: 10.1021/mp100464y</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Doz E, Rose S, Nigou J, Gilleron M, Puzo G, Erard F, et al. Acylation Determines the Toll-Like Receptor (TLR)- Dependent Positive Versus TLR2-, Mannose Receptor-, and SIGNR1- Independent Negative Regulation of Proinflammatory Cytokines by Mycobacterial Lipomannan. J Biol Chem. 2007; 282(36):26014–25. DOI: 10.1074/jbc.M702690200</mixed-citation><mixed-citation xml:lang="en">Doz E, Rose S, Nigou J, Gilleron M, Puzo G, Erard F, et al. Acylation Determines the Toll-Like Receptor (TLR)- Dependent Positive Versus TLR2-, Mannose Receptor-, and SIGNR1- Independent Negative Regulation of Proinflammatory Cytokines by Mycobacterial Lipomannan. J Biol Chem. 2007; 282(36):26014–25. DOI: 10.1074/jbc.M702690200</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Yamamura Y, Azuma I, Sugimura K, Yamawaki M, Uemiya M. Adjuvant Activity of 6-O- mycoloyl-N-acetylmuramuyl-Lalanyl- D-isoglutamine. Gan 1976;67(6):867–77.</mixed-citation><mixed-citation xml:lang="en">Yamamura Y, Azuma I, Sugimura K, Yamawaki M, Uemiya M. Adjuvant Activity of 6-O- mycoloyl-N-acetylmuramuyl-Lalanyl- D-isoglutamine. Gan 1976;67(6):867–77.</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Azuma I, Okumura H, Saiki I, Kiso M, Hasegawa A, Tanio Y, Yamamura Y. Adjuvant Activity of Carbohydrate Analogs of N-acetylmuramyl-L-alanyl-D-isoglutamine on the Induction of Delayed-Type Hypersensitivity to Azobenzenearsonate- N-acetyl-L-tyrosine in Guinea Pigs. Infect Immun. 1981;33(3):834–39.</mixed-citation><mixed-citation xml:lang="en">Azuma I, Okumura H, Saiki I, Kiso M, Hasegawa A, Tanio Y, Yamamura Y. Adjuvant Activity of Carbohydrate Analogs of N-acetylmuramyl-L-alanyl-D-isoglutamine on the Induction of Delayed-Type Hypersensitivity to Azobenzenearsonate- N-acetyl-L-tyrosine in Guinea Pigs. Infect Immun. 1981;33(3):834–39.</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Masihi KN, Lange W, Brehmer W, Ribi E. Immunobiological Activities of Nontoxic Lipid A: Enhancement of Nonspecific Resistance in Combination with Trehalose Dimycolate against Viral Infection and Adjuvant Effects. Int J Immunopharmacol. 1986;8(3):339–45.</mixed-citation><mixed-citation xml:lang="en">Masihi KN, Lange W, Brehmer W, Ribi E. Immunobiological Activities of Nontoxic Lipid A: Enhancement of Nonspecific Resistance in Combination with Trehalose Dimycolate against Viral Infection and Adjuvant Effects. Int J Immunopharmacol. 1986;8(3):339–45.</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Cekic C, Casella CR, Eaves CA, Matsuzawa A, Ichijo H, Mitchell TC. Selective Activation of the p38 MAPK Pathway by Synthetic Monophosphoryl Lipid A. J Biol Chem. 2009;284(46):31982–91. DOI: 10.1074/jbc.M109.046383</mixed-citation><mixed-citation xml:lang="en">Cekic C, Casella CR, Eaves CA, Matsuzawa A, Ichijo H, Mitchell TC. Selective Activation of the p38 MAPK Pathway by Synthetic Monophosphoryl Lipid A. J Biol Chem. 2009;284(46):31982–91. DOI: 10.1074/jbc.M109.046383</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Schiller JT, Castellsague X, Villa LL, Hildesheim A. An Update of Prophylactic Human Papillomavirus L1 Virus-Like Particle Vaccine Clinical Trial Results. Vaccine 2008;26(Suppl 10):K53–K61. DOI: 10.1016/j.vaccine.2008.06.002</mixed-citation><mixed-citation xml:lang="en">Schiller JT, Castellsague X, Villa LL, Hildesheim A. An Update of Prophylactic Human Papillomavirus L1 Virus-Like Particle Vaccine Clinical Trial Results. Vaccine 2008;26(Suppl 10):K53–K61. DOI: 10.1016/j.vaccine.2008.06.002</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Quan FS, Ko EJ, Kwon YM, Joo KH, Compans RW, Kang SM. Mucosal Adjuvants for Influenza Virus-Like Particle Vaccine. Viral Immunol. 2013;26(6):385–95. DOI: 10.1089/vim.2013.0013</mixed-citation><mixed-citation xml:lang="en">Quan FS, Ko EJ, Kwon YM, Joo KH, Compans RW, Kang SM. Mucosal Adjuvants for Influenza Virus-Like Particle Vaccine. Viral Immunol. 2013;26(6):385–95. DOI: 10.1089/vim.2013.0013</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Lacaille-Dubois M-A. Bioactive Saponins with Cancer Related and Immunomodulatory Activity: Recent Developments. In: Atta-ur-Rahman, ed. Bioactive Natural Products. Amsterdam: Elsevier; 2005. Vol. 32, Part L, P. 209–246. DOI: 10.1016/s1572-5995(05)80057-2.</mixed-citation><mixed-citation xml:lang="en">Lacaille-Dubois M-A. Bioactive Saponins with Cancer Related and Immunomodulatory Activity: Recent Developments. In: Atta-ur-Rahman, ed. Bioactive Natural Products. Amsterdam: Elsevier; 2005. Vol. 32, Part L, P. 209–246. DOI: 10.1016/s1572-5995(05)80057-2.</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Kensil CR, Wu JY, Soltysik S. Structural and Immunological Characterization of the Vaccine Adjuvant QS-21. Pharm Biotechnol. 1995;6:525–41.</mixed-citation><mixed-citation xml:lang="en">Kensil CR, Wu JY, Soltysik S. Structural and Immunological Characterization of the Vaccine Adjuvant QS-21. Pharm Biotechnol. 1995;6:525–41.</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Pham HL, Ross BP, McGeary RP, Shaw PN, Hewavitharana AK, Davies NM. Saponins from Quillaja Saponaria Molina: Isolation, Characterization and Ability to Form Immuno Stimulatory Complexes (ISCOMs). Curr Drug Deliv. 2006;3(4):389–97.</mixed-citation><mixed-citation xml:lang="en">Pham HL, Ross BP, McGeary RP, Shaw PN, Hewavitharana AK, Davies NM. Saponins from Quillaja Saponaria Molina: Isolation, Characterization and Ability to Form Immuno Stimulatory Complexes (ISCOMs). Curr Drug Deliv. 2006;3(4):389–97.</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Quenelle DC, Collins DJ, Rice TL, Prichard MN, Marciani DJ, Kern ER. Effect of an Immune Enhancer, GPI-0100, on Vaccination with Live Attenuated Herpes Simplex Virus (HSV) Type 2 or Glycoprotein D on Genital HSV-2 Infections of Guinea Pigs. Antiviral Res. 2008;80(2):223–4. DOI:</mixed-citation><mixed-citation xml:lang="en">Quenelle DC, Collins DJ, Rice TL, Prichard MN, Marciani DJ, Kern ER. Effect of an Immune Enhancer, GPI-0100, on Vaccination with Live Attenuated Herpes Simplex Virus (HSV) Type 2 or Glycoprotein D on Genital HSV-2 Infections of Guinea Pigs. Antiviral Res. 2008;80(2):223–4. DOI:</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">1016/j.antiviral.2008.05.011</mixed-citation><mixed-citation xml:lang="en">1016/j.antiviral.2008.05.011</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Ragupathi G, Coltart DM, Williams LJ, Koide F, Kagan E, Allen J, et al. On the Power of Chemical Synthesis: Immunological Evaluation of Models for Multiantigenic Carbohydrate- Based Cancer Vaccines. Proc Natl Acad Sci U S A 2002;99(21):13699–704. DOI: 10.1073/pnas.202427599</mixed-citation><mixed-citation xml:lang="en">Ragupathi G, Coltart DM, Williams LJ, Koide F, Kagan E, Allen J, et al. On the Power of Chemical Synthesis: Immunological Evaluation of Models for Multiantigenic Carbohydrate- Based Cancer Vaccines. Proc Natl Acad Sci U S A 2002;99(21):13699–704. DOI: 10.1073/pnas.202427599</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Raphael TJ, Kuttan G. Effect of Naturally Occurring Triterpenoids Glycyrrhizic Acid, Ursolic Acid, Oleanolic Acid and Nomilin on the Immune System. Phytomedicine 2003;10(6–7):483–9. DOI: 10.1078/094471103322331421</mixed-citation><mixed-citation xml:lang="en">Raphael TJ, Kuttan G. Effect of Naturally Occurring Triterpenoids Glycyrrhizic Acid, Ursolic Acid, Oleanolic Acid and Nomilin on the Immune System. Phytomedicine 2003;10(6–7):483–9. DOI: 10.1078/094471103322331421</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Newman MJ, Wu JY, Gardner BH, Anderson CA, Kensil CR, Recchia J, et al. Induction of Cross-Reactive Cytotoxic T-lymphocyte Responses Specific for HIV-1 gp120 Using Saponin Adjuvant (QS-21) Supplemented Subunit Vaccine Formulations. Vaccine 1997;15(9):1001–7.</mixed-citation><mixed-citation xml:lang="en">Newman MJ, Wu JY, Gardner BH, Anderson CA, Kensil CR, Recchia J, et al. Induction of Cross-Reactive Cytotoxic T-lymphocyte Responses Specific for HIV-1 gp120 Using Saponin Adjuvant (QS-21) Supplemented Subunit Vaccine Formulations. Vaccine 1997;15(9):1001–7.</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Sasaki S, Sumino K, Hamajima K, Fukushima J, Ishii N, Kawamoto S, et al. Induction of Systemic and Mucosal Immune Responses to Human Immunodeficiency Virus Type 1 by a DNA Vaccine Formulated with QS-21 Saponin Adjuvant via Intramuscular and Intranasal Routes. J Virol. 1998;72(6):4931–9.</mixed-citation><mixed-citation xml:lang="en">Sasaki S, Sumino K, Hamajima K, Fukushima J, Ishii N, Kawamoto S, et al. Induction of Systemic and Mucosal Immune Responses to Human Immunodeficiency Virus Type 1 by a DNA Vaccine Formulated with QS-21 Saponin Adjuvant via Intramuscular and Intranasal Routes. J Virol. 1998;72(6):4931–9.</mixed-citation></citation-alternatives></ref><ref id="cit76"><label>76</label><citation-alternatives><mixed-citation xml:lang="ru">Lee JK, Lee MK, Yun YP, Kim Y, Kim JS, Kim YS, et al. Acemannan Purified from Aloe Vera Induces Phenotypic and Functional Maturation of Immature Dendritic Cells. Int Immunopharmacol. 2001;1(7):1275–84.</mixed-citation><mixed-citation xml:lang="en">Lee JK, Lee MK, Yun YP, Kim Y, Kim JS, Kim YS, et al. Acemannan Purified from Aloe Vera Induces Phenotypic and Functional Maturation of Immature Dendritic Cells. Int Immunopharmacol. 2001;1(7):1275–84.</mixed-citation></citation-alternatives></ref><ref id="cit77"><label>77</label><citation-alternatives><mixed-citation xml:lang="ru">Bohana-Kashtan O, Ziporen L, Donin N, Kraus S, Fishelson Z. Cell Signals Transduced by Complement. Mol Immunol. 2004;41(6–7):583–97. DOI: 10.1016/j.molimm.2004.04.007</mixed-citation><mixed-citation xml:lang="en">Bohana-Kashtan O, Ziporen L, Donin N, Kraus S, Fishelson Z. Cell Signals Transduced by Complement. Mol Immunol. 2004;41(6–7):583–97. DOI: 10.1016/j.molimm.2004.04.007</mixed-citation></citation-alternatives></ref><ref id="cit78"><label>78</label><citation-alternatives><mixed-citation xml:lang="ru">Rawal N, Rajagopalan R, Salvi VP. Stringent Regulation of Complement Lectin Pathway C3/C5 Convertase by C4bbinding Protein (C4BP). Mol Immunol. 2009;46(15):2902–10. DOI: 10.1016/j.molimm.2009.07.006</mixed-citation><mixed-citation xml:lang="en">Rawal N, Rajagopalan R, Salvi VP. Stringent Regulation of Complement Lectin Pathway C3/C5 Convertase by C4bbinding Protein (C4BP). Mol Immunol. 2009;46(15):2902–10. DOI: 10.1016/j.molimm.2009.07.006</mixed-citation></citation-alternatives></ref><ref id="cit79"><label>79</label><citation-alternatives><mixed-citation xml:lang="ru">Weston SA, Parish CR. Modification of Lymphocyte Migration by Mannans and Phosphomannans. Different Carbohydrate Structures Control Entry of Lymphocytes into Spleen and Lymph Nodes. J Immunol. 1991;146(12):4180–6.</mixed-citation><mixed-citation xml:lang="en">Weston SA, Parish CR. Modification of Lymphocyte Migration by Mannans and Phosphomannans. Different Carbohydrate Structures Control Entry of Lymphocytes into Spleen and Lymph Nodes. J Immunol. 1991;146(12):4180–6.</mixed-citation></citation-alternatives></ref><ref id="cit80"><label>80</label><citation-alternatives><mixed-citation xml:lang="ru">Dong SF, Chen JM, Zhang W, Sun SH, Wang J, Gu JX, et al. Specific Immune Response to HBsAg is Enhanced by Beta-glucan Oligosaccharide Containing an alpha-(1–&gt;3)linked Bond and Biased towards M2/Th2. Int Immunopharmacol. 2007;7(6):725–33. DOI: 10.1016/j.intimp.2007.01.004</mixed-citation><mixed-citation xml:lang="en">Dong SF, Chen JM, Zhang W, Sun SH, Wang J, Gu JX, et al. Specific Immune Response to HBsAg is Enhanced by Beta-glucan Oligosaccharide Containing an alpha-(1–&gt;3)linked Bond and Biased towards M2/Th2. Int Immunopharmacol. 2007;7(6):725–33. DOI: 10.1016/j.intimp.2007.01.004</mixed-citation></citation-alternatives></ref><ref id="cit81"><label>81</label><citation-alternatives><mixed-citation xml:lang="ru">Petrovsky N, Cooper PD. Advax™, a Novel Microcrystalline Polysaccharide Particle Engineered from Delta Inulin, Provides Robust Adjuvant Potency together with Tolerability and Safety. Vaccine 2015;33(44):5920–6. DOI: 10.1016/j.vaccine.2015.09.030</mixed-citation><mixed-citation xml:lang="en">Petrovsky N, Cooper PD. Advax™, a Novel Microcrystalline Polysaccharide Particle Engineered from Delta Inulin, Provides Robust Adjuvant Potency together with Tolerability and Safety. Vaccine 2015;33(44):5920–6. DOI: 10.1016/j.vaccine.2015.09.030</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
