Chemokines: Key players in innate and adaptive immunity

被引:288
作者
Esche, C
Stellato, C
Beck, LA
机构
[1] Johns Hopkins Asthma & Allergy Ctr, Div Clin Immunol & Allergy, Baltimore, MD 21224 USA
[2] Johns Hopkins Univ, Dept Dermatol, Baltimore, MD 21218 USA
关键词
adaptive; chemokine; inflammation; innate;
D O I
10.1111/j.0022-202X.2005.23841.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Healthy individuals initiate an immediate immune response to microbes by using a set of germline-encoded receptors that recognize common molecular patterns found on the surface of pathogens that are distinct from self-antigens. This innate immune response is the first line of defense against microorganisms in vertebrates, and constitutes the only immune response in plants and invertebrates. The innate immune system includes cellular components, as well as a host of soluble products (antimicrobial peptides, complement fragments, cytokines, and chemokines). The adaptive immune response, which provides long-lasting protection, takes days to develop and requires somatic mutations leading to the development of antigen-specific T cell receptors (cell-mediated immunity) and immunoglobulins (humoral immunity). Members of the chemokine superfamily are crucially involved in both innate and adaptive responses. We review the biological actions of the chemokine superfamily, focusing on several functions that are relevant for both immune responses, such as cell recruitment, microbicidal activity, cell activation, polarization of CD4(+) T cells, and effects on structural cells. In particular, we will illustrate the central role that chemokines play in host defense, best demonstrated by the tremendous number of chemokine and chemokine receptor homologs found in microbial genomes, which deflect the immune response of the host.
引用
收藏
页码:615 / 628
页数:14
相关论文
共 83 条
[1]   THE INTEGRIN VLA-4 SUPPORTS TETHERING AND ROLLING IN FLOW ON VCAM-1 [J].
ALON, R ;
KASSNER, PD ;
CARR, MW ;
FINGER, EB ;
HEMLER, ME ;
SPRINGER, TA .
JOURNAL OF CELL BIOLOGY, 1995, 128 (06) :1243-1253
[2]   C-C chemokine receptor 4 expression defines a major subset of circulating nonintestinal memory T cells of both Th1 and Th2 potential [J].
Andrew, DP ;
Ruffing, N ;
Kim, CH ;
Miao, WY ;
Heath, H ;
Li, Y ;
Murphy, K ;
Campbell, JJ ;
Butcher, EC ;
Wu, LJ .
JOURNAL OF IMMUNOLOGY, 2001, 166 (01) :103-111
[3]  
Beck Lisa A., 2000, Journal of Allergy and Clinical Immunology, V106, pS258
[4]   Chemokine receptors as HIV-1 coreceptors: Roles in viral entry, tropism, and disease [J].
Berger, EA ;
Murphy, PM ;
Farber, JM .
ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 :657-700
[5]   Road signs guiding leukocytes along the inflammation superhighway [J].
Bochner, BS .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2000, 106 (05) :817-828
[6]   Responses of leukocytes to chemokines in whole blood and their antagonism by novel CC-chemokine receptor 3 antagonists [J].
Bryan, SA ;
Jose, PJ ;
Topping, JR ;
Wilhelm, R ;
Soderberg, C ;
Kertesz, D ;
Barnes, PJ ;
Williams, TJ ;
Hansel, TT ;
Sabroe, I .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 165 (12) :1602-1609
[7]   Unique subpopulations of CD56+ NK and NK-T peripheral blood lymphocytes identified by chemokine receptor expression repertoire [J].
Campbell, JJ ;
Qin, SX ;
Unutmaz, D ;
Soler, D ;
Murphy, KE ;
Hodge, MR ;
Wu, LJ ;
Butcher, EC .
JOURNAL OF IMMUNOLOGY, 2001, 166 (11) :6477-6482
[8]   Dendritic cell biology and regulation of dendritic cell trafficking by chemokines [J].
Caux, C ;
Ait-Yahia, S ;
Chemin, K ;
de Bouteiller, O ;
Dieu-Nosjean, MC ;
Homey, B ;
Massacrier, C ;
Vanbervliet, B ;
Zlotnik, A ;
Vicari, A .
SPRINGER SEMINARS IN IMMUNOPATHOLOGY, 2000, 22 (04) :345-369
[9]   Cutting edge:: IFN-inducible ELR- CXC chemokines display defensin-like antimicrobial activity [J].
Cole, AM ;
Ganz, T ;
Liese, AM ;
Burdick, MD ;
Liu, L ;
Strieter, RM .
JOURNAL OF IMMUNOLOGY, 2001, 167 (02) :623-627
[10]   Post-translational control of chemokines: a role for,decoy receptors? [J].
Comerford, L ;
Nibbs, RJB .
IMMUNOLOGY LETTERS, 2005, 96 (02) :163-174