Variegation of the immune response with dendritic cells and pathogen recognition receptors

被引:124
作者
Pulendran, B
机构
[1] Emory Univ, Vaccine Res Ctr, Atlanta, GA 30329 USA
[2] Emory Univ, Dept Pathol, Atlanta, GA 30329 USA
关键词
D O I
10.4049/jimmunol.174.5.2457
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
One of the most fundamental questions in biology is: "How do cells differentiate in the right place, at the right time, into the right kinds?" Understanding the phenomenon of cell differentiation in its spatial and temporal framework is a prelude to understanding the development and physiology of all multicellular systems, including the immune system. Insights over the past 2300 years, since Aristotle, suggest that biological differentiation is guided by the interplay between genetic programs and specific environmental signals. This is exemplified by the mammalian immune response to pathogens, where qualitatively different types can emerge. Although it is appreciated that this type immunity is critical for optimal defense against different pathogens, the early "decision-making mechanisms" are largely obscure. Recent developments in innate immunity and genomics, especially in the biology of dendritic cells (DCs) and pathogen recognition receptors, have stimulated intense research in understanding the mechanisms guiding the differentiation of Th1, Th2, and T regulatory responses. In this study, I summarize recent findings which suggest that activation of DCs via distinct pathogen recognition receptors stimulate different gene expression programs and signaling networks in DCs that guide the variegation ofimmune responses.
引用
收藏
页码:2457 / 2465
页数:9
相关论文
共 107 条
[41]   The plasticity of dendritic cell responses to pathogens and their components [J].
Huang, Q ;
Liu, DY ;
Majewski, P ;
Schulte, LC ;
Korn, JM ;
Young, RA ;
Lander, ES ;
Hacohen, N .
SCIENCE, 2001, 294 (5543) :870-875
[42]  
Hubel D., 1995, Eye, Brain and Vision
[43]   Freshly isolated Peyer's patch, but not spleen, dendritic cells produce interleukin 10 and induce the differentiation of T helper type 2 cells [J].
Iwasaki, A ;
Kelsall, BL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (02) :229-239
[44]  
JANEWAY CA, 1989, COLD SH Q B, V54, P1
[45]   Innate immune recognition [J].
Janeway, CA ;
Medzhitov, R .
ANNUAL REVIEW OF IMMUNOLOGY, 2002, 20 :197-216
[46]  
Jarrossay D, 2001, EUR J IMMUNOL, V31, P3388, DOI 10.1002/1521-4141(200111)31:11<3388::AID-IMMU3388>3.0.CO
[47]  
2-Q
[48]   Human dendritic cells respond to Porphyromonas gingivalis LPS by promoting a Th2 effector response in vitro [J].
Jotwani, R ;
Pulendran, B ;
Agrawal, S ;
Cutler, CW .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2003, 33 (11) :2980-2986
[49]   Subsets of human dendritic cell precursors express different toll-like receptors and respond to different microbial antigens [J].
Kadowaki, N ;
Ho, S ;
Antonenko, S ;
Malefyt, RD ;
Kastelein, RA ;
Bazan, F ;
Liu, YJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (06) :863-869
[50]   Effector and memory T-cell differentiation: Implications for vaccine development [J].
Kaech, SM ;
Wherry, EJ ;
Ahmed, R .
NATURE REVIEWS IMMUNOLOGY, 2002, 2 (04) :251-262