Bacterial Protein Toll-Like-Receptor Agonists: A Novel Perspective on Vaccine Adjuvants

被引:90
作者
Kumar, Sudeep [1 ]
Sunagar, Raju [2 ]
Gosselin, Edmund [1 ]
机构
[1] Albany Med Coll, Dept Immunol & Microbial Dis, Albany, NY 12208 USA
[2] Genome Valley, Ella Fdn, Hyderabad, India
关键词
adjuvant; TLR agonist; TLR; antigen presenting cells; cell-mediated immunity; vaccine; ACTIVATES DENDRITIC CELLS; PERTUSSIS FILAMENTOUS HEMAGGLUTININ; SHIGELLA-FLEXNERI; 2A; TH1; IMMUNE-RESPONSE; PHAGOSOME MATURATION; ALUMINUM-HYDROXIDE; ADAPTIVE IMMUNITY; INNATE IMMUNITY; IN-VIVO; A OMPA;
D O I
10.3389/fimmu.2019.01144
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Adjuvants have been used in vaccines for over a century, however, the search for safe and effective vaccine adjuvants continues. In recent decades toll-like-receptor (TLR) agonists have been investigated as potential vaccine adjuvants. In this regard, the majority of the currently investigated TLR agonists are non-protein microbial components such as lipopolysaccharides, oligonucleotides, and lipopeptides. On the other hand, a growing number of studies reveal that TLR signaling and immune responses can be activated by numerous bacterial proteins. However, their potential roles as adjuvants have been somewhat overlooked. Herein, we discuss several such bacterial proteins which exhibit adjuvant properties, including the activation of TLR signaling, antigen presenting cell maturation, pro-inflammatory cytokine production and adaptive immune response. The protein nature of these TLR agonists presents several unique features not shared by non-protein TLR agonists. These properties include the amenability for modifying the structure and function as necessary for optimal immunogenicity and minimal toxicity. Protein adjuvants can be genetically fused to protein antigens which ensure the co-delivery of adjuvant-antigen not only into the same cell but also in the same endocytic cargo, leading to more effective activation of innate and adaptive immune response.
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页数:8
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共 81 条
[21]   Flagellin as a vaccine adjuvant [J].
Cui, Baofeng ;
Liu, Xinsheng ;
Fang, Yuzhen ;
Zhou, Peng ;
Zhang, Yongguang ;
Wang, Yonglu .
EXPERT REVIEW OF VACCINES, 2018, 17 (04) :335-349
[22]   TLR4 Mediates Pneumolysin-Induced ATF3 Expression through the JNK/p38 Pathway in Streptococcus pneumoniae-Infected RAW 264.7 Cells [J].
Cuong Thach Nguyen ;
Kim, Eun-Hye ;
Truc Thanh Luong ;
Pyo, Suhkneung ;
Rhee, Dong-Kwon .
MOLECULES AND CELLS, 2015, 38 (01) :58-64
[23]   Correlates of adjuvanticity: A review on adjuvants in licensed vaccines [J].
Del Giudice, Giuseppe ;
Rappuoli, Rino ;
Didierlaurent, Arnaud M. .
SEMINARS IN IMMUNOLOGY, 2018, 39 (0C) :14-21
[24]   Vaccines for the 21st century [J].
Delany, Isabel ;
Rappuoli, Rino ;
De Gregorio, Ennio .
EMBO MOLECULAR MEDICINE, 2014, 6 (06) :708-720
[25]   Vaccination in the elderly [J].
Derhovanessian, Evelyna ;
Pawelec, Graham .
MICROBIAL BIOTECHNOLOGY, 2012, 5 (02) :226-232
[26]   Polarization of naive T cells into Th1 or Th2 by distinct cytokine-driven murine dendritic cell populations: implications for immunotherapy [J].
Feili-Hariri, M ;
Falkner, DH ;
Morel, PA .
JOURNAL OF LEUKOCYTE BIOLOGY, 2005, 78 (03) :656-664
[27]   The contribution of vaccination to global health: past, present and future [J].
Greenwood, Brian .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2014, 369 (1645)
[28]   Bacterial flagellin-a potent immunomodulatory agent [J].
Hajam, Irshad A. ;
Dar, Pervaiz A. ;
Shahnawaz, Imam ;
Jaume, Juan Carlos ;
Lee, John Hwa .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2017, 49 :e373-e373
[29]   Endocytic pathways regulate Toll-like receptor 4 signaling and link innate and adaptive immunity [J].
Husebye, H ;
Halaas, O ;
Stenmark, H ;
Tunheim, G ;
Sandanger, O ;
Bogen, B ;
Brech, A ;
Latz, E ;
Espevik, T .
EMBO JOURNAL, 2006, 25 (04) :683-692
[30]   Innate immune recognition [J].
Janeway, CA ;
Medzhitov, R .
ANNUAL REVIEW OF IMMUNOLOGY, 2002, 20 :197-216