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
[11]   Chemokines trigger immediate β2 integrin affinity and mobility changes:: Differential regulation and roles in lymphocyte arrest under flow [J].
Constantin, G ;
Majeed, M ;
Giagulli, C ;
Piccio, L ;
Kim, JY ;
Butcher, EC ;
Laudanna, C .
IMMUNITY, 2000, 13 (06) :759-769
[12]   Structure/function of human herpesvirus-8 MIP-II (1-71) and the antagonist N-terminal segment (1-10) [J].
Crump, MP ;
Elisseeva, E ;
Gong, JH ;
Clark-Lewis, I ;
Sykes, BD .
FEBS LETTERS, 2001, 489 (2-3) :171-175
[13]   Exaggerated response to endotoxin in mice lacking the Duffy antigen/receptor for chemokines (DARC) [J].
Dawson, TC ;
Lentsch, AB ;
Wang, ZX ;
Cowhig, JE ;
Rot, A ;
Maeda, N ;
Peiper, SC .
BLOOD, 2000, 96 (05) :1681-1684
[14]   Macrophage inflammatory protein 3α is expressed at inflamed epithelial surfaces and is the most potent chemokine known in attracting Langerhans cell precursors [J].
Dieu-Nosjean, MC ;
Massacrier, C ;
Homey, B ;
Vanbervliet, B ;
Pin, JJ ;
Vicari, A ;
Lebecque, S ;
Dezutter-Dambuyant, C ;
Schmitt, D ;
Zlotnik, A ;
Caux, C .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (05) :705-717
[15]   What is the real role of antimicrobial polypeptides that can mediate several other inflammatory responses? [J].
Elsbach, P .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (11) :1643-1645
[16]   Cutting edge:: Scavenging of inflammatory CC chemokines by the promiscuous putatively silent chemokine receptor D61 [J].
Fra, AM ;
Locati, M ;
Otero, K ;
Sironi, M ;
Signorelli, P ;
Massardi, ML ;
Gobbi, M ;
Vecchi, A ;
Sozzani, S ;
Mantovani, A .
JOURNAL OF IMMUNOLOGY, 2003, 170 (05) :2279-2282
[17]   Presence of high contents of thymus and activation-regulated chemokine in platelets and elevated plasma levels of thymus and activation-regulated chemokine and macrophage-derived chemokine in patients with atopic dermatitis [J].
Fujisawa, T ;
Fujisawa, R ;
Kato, Y ;
Nakayama, T ;
Morita, A ;
Katsumata, H ;
Nishimori, H ;
Iguchi, K ;
Kamiya, H ;
Gray, PW ;
Chantry, D ;
Suzuki, R ;
Yoshie, O .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2002, 110 (01) :139-146
[18]   Negative regulation of eosinophil recruitment to the lung by the chemokine monokine induced by IFN-γ (Mig, CXCL9) [J].
Fulkerson, PC ;
Zimmermann, N ;
Brandt, EB ;
Muntel, EE ;
Doepker, MP ;
Kavanaugh, JL ;
Mishra, A ;
Witte, DP ;
Zhang, HW ;
Farber, JM ;
Yang, M ;
Foster, PS ;
Rothenberg, ME .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (07) :1987-1992
[19]  
Galli G, 2000, EUR J IMMUNOL, V30, P204, DOI 10.1002/1521-4141(200001)30:1<204::AID-IMMU204>3.3.CO
[20]  
2-7