Translating innate immunity into immunological memory: Implications for vaccine development

被引:471
作者
Pulendran, B
Ahmed, R
机构
[1] Emory Vaccine Ctr, Dept Pathol, Atlanta, GA 30329 USA
[2] Emory Vaccine Ctr, Dept Microbiol & Immunol, Atlanta, GA 30329 USA
关键词
D O I
10.1016/j.cell.2006.02.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vaccination is the most effective means of preventing infectious diseases. Despite the success of many vaccines, there is presently little knowledge of the immunological mechanisms that mediate their efficacy. Such information will be critical in the design of future vaccines against old and new infectious diseases. Recent advances in immunology are beginning to provide an intellectual framework with which to address fundamental questions about how the innate immune system shapes adaptive immunity. In this review, we summarize current knowledge about how the innate immune system modulates the quantity and quality of longterm T and B cell memory and protective immune responses to pathogens. In addition, we point out unanswered questions and identify critical challenges, the solution of which, we believe, will greatly facilitate the rational design of novel vaccines against a multitude of emerging infections.
引用
收藏
页码:849 / 863
页数:15
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共 108 条
[1]   Systems biology: Its practice and challenges [J].
Aderem, A .
CELL, 2005, 121 (04) :511-513
[2]   Impairment of dendritic cells and adaptive immunity by anthrax lethal toxin [J].
Agrawal, A ;
Lingappa, J ;
Leppla, SH ;
Agrawal, S ;
Jabbar, A ;
Quinn, C ;
Pulendran, B .
NATURE, 2003, 424 (6946) :329-334
[3]   Cutting edge: Different toll-like receptor agonists instruct dendritic cells to induce distinct th responses via differential modulation of extracellular signal-regulated kinase-mitogen-activated protein kinase and c-fos [J].
Agrawal, S ;
Agrawal, A ;
Doughty, B ;
Gerwitz, A ;
Blenis, J ;
Van Dyke, T ;
Pulendran, B .
JOURNAL OF IMMUNOLOGY, 2003, 171 (10) :4984-4989
[4]   Immunological memory and protective immunity: Understanding their relation [J].
Ahmed, R ;
Gray, D .
SCIENCE, 1996, 272 (5258) :54-60
[5]   Pathogen recognition and innate immunity [J].
Akira, S ;
Uematsu, S ;
Takeuchi, O .
CELL, 2006, 124 (04) :783-801
[6]   Immunobiology of dendritic cells [J].
Banchereau, J ;
Briere, F ;
Caux, C ;
Davoust, J ;
Lebecque, S ;
Liu, YT ;
Pulendran, B ;
Palucka, K .
ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 :767-+
[7]   Restoring function in exhausted CD8 T cells during chronic viral infection [J].
Barber, DL ;
Wherry, EJ ;
Masopust, D ;
Zhu, BG ;
Allison, JP ;
Sharpe, AH ;
Freeman, GJ ;
Ahmed, R .
NATURE, 2006, 439 (7077) :682-687
[8]   Inherent specificities in natural antibodies: a key to immune defense against pathogen invasion [J].
Baumgarth, N ;
Tung, JW ;
Herzenberg, LA .
SPRINGER SEMINARS IN IMMUNOPATHOLOGY, 2005, 26 (04) :347-362
[9]   Bone marrow is a preferred site for homeostatic proliferation of memory CD8 T cells [J].
Becker, TC ;
Coley, SM ;
Wherry, EJ ;
Ahmed, R .
JOURNAL OF IMMUNOLOGY, 2005, 174 (03) :1269-1273
[10]   Maintenance of serological memory by polyclonal activation of human memory B cells [J].
Bernasconi, NL ;
Traggiai, E ;
Lanzavecchia, A .
SCIENCE, 2002, 298 (5601) :2199-2202