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
[21]   Defensins: Antimicrobial peptides of innate immunity [J].
Ganz, T .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (09) :710-720
[22]   The human Duffy antigen binds selected inflammatory but not homeostatic chemokines [J].
Gardner, L ;
Patterson, AM ;
Ashton, BA ;
Stone, MA ;
Middleton, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 321 (02) :306-312
[23]   Chemokines and disease [J].
Gerard, C ;
Rollins, BJ .
NATURE IMMUNOLOGY, 2001, 2 (02) :108-115
[24]   Antimicrobial psoriasin (S100A7) protects human skin from Escherichia coli infection [J].
Gläser, R ;
Harder, J ;
Lange, H ;
Bartels, J ;
Christophers, E ;
Schröder, JM .
NATURE IMMUNOLOGY, 2005, 6 (01) :57-64
[25]   Transepithelial neutrophil migration is CXCR1 dependent in vitro and is defective in IL-8 receptor knockout mice [J].
Godaly, G ;
Hang, L ;
Frendéus, B ;
Svanborg, C .
JOURNAL OF IMMUNOLOGY, 2000, 165 (09) :5287-5294
[26]   Mice lacking expression of secondary lymphoid organ chemokine have defects in lymphocyte homing and dendritic cell localization [J].
Gunn, MD ;
Kyuwa, S ;
Tam, C ;
Kakiuchi, T ;
Matsuzawa, A ;
Williams, LT ;
Nakano, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (03) :451-460
[27]   CCL28 has dual roles in mucosal immunity as a chemokine with broad-spectrum antimicrobial activity [J].
Hieshima, K ;
Ohtani, H ;
Shibano, M ;
Izawa, D ;
Nakayama, T ;
Kawasaki, Y ;
Shiba, F ;
Shiota, M ;
Katou, F ;
Saito, T ;
Yoshie, O .
JOURNAL OF IMMUNOLOGY, 2003, 170 (03) :1452-1461
[28]   Up-regulation of macrophage inflammatory protein-3α/CCL20 and CC chemokine receptor 6 in psoriasis [J].
Homey, B ;
Dieu-Nosjean, MC ;
Wiesenborn, A ;
Massacrier, C ;
Pin, JJ ;
Oldham, E ;
Catron, D ;
Buchanan, ME ;
Müller, A ;
Malefyt, RD ;
Deng, G ;
Orozco, R ;
Ruzicka, T ;
Lehmann, P ;
Lebecque, S ;
Caux, C ;
Zlotnik, A .
JOURNAL OF IMMUNOLOGY, 2000, 164 (12) :6621-6632
[29]   CCL27-CCR10 interactions regulate T cell-mediated skin inflammation [J].
Homey, B ;
Alenius, H ;
Müller, A ;
Soto, H ;
Bowman, EP ;
Yuan, W ;
McEvoy, L ;
Lauerma, AI ;
Assmann, T ;
Bünemann, E ;
Lehto, M ;
Wolff, H ;
Yen, D ;
Marxhausen, H ;
To, W ;
Sedgwick, J ;
Ruzicka, T ;
Lehmann, P ;
Zlotnik, A .
NATURE MEDICINE, 2002, 8 (02) :157-165
[30]   The structure of human macrophage inflammatory protein-3α/CCL20 -: Linking antimicrobial and CC chemokine receptor-6-binding activities with human β-defensins [J].
Hoover, DM ;
Boulègue, C ;
Yang, D ;
Oppenheim, JJ ;
Tucker, K ;
Lu, WY ;
Lubkowski, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (40) :37647-37654