Glycolipid targets of CD1-mediated T-cell responses

被引:25
作者
Moody, DB
Besra, GS
机构
[1] Univ Newcastle Upon Tyne, Sch Med, Dept Microbiol & Immunol, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[2] Brigham & Womens Hosp, Div Rheumatol Immunol & Allergy, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
关键词
D O I
10.1046/j.1365-2567.2001.01326.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Members of the CD1 family of antigen-presenting molecules bind and present a variety of mammalian and microbial glycolipids for specific recognition by T cells. CD I proteins accomplish their antigen-presenting function by binding the alkyl chains of the antigens within a deep. hydrophobic groove on the membrane distal surface of CD1, making the hydrophilic element, of the antigen available for contact with the variable regions of antigen-specific T-cell receptors. Most models of CD1-restricted T cells function in infectious. neoplastic, or a autoimmune diseases and are based on the premise that CD1-restricted T-cell responses are initiated by alterations in Cellular glycolipid content. Although a growing number of self, altered self and foreign glycolipid antigens have been identified, the cellular mechanisms that Could lead to the generation of antigenic glycolipids within cells, or control the presentation of particular classes of altered self or microbial glycolipids in disease states have only recently come under investigation. Here we review the Structures of known glycolipid antigens for T cells and discuss how the chemical nature of these antigens, which is quite different from that of peptides. influences their recognition by T cells.
引用
收藏
页码:243 / 251
页数:9
相关论文
共 73 条
[51]  
Park SH, 1998, J IMMUNOL, V160, P3128
[52]   Human T cells expressing an invariant V alpha 24-J alpha Q TCR alpha are CD4- and heterogeneous with respect to TCR beta expression [J].
Porcelli, S ;
Gerdes, D ;
Fertig, AM ;
Balk, SP .
HUMAN IMMUNOLOGY, 1996, 48 (1-2) :63-67
[53]   RECOGNITION OF CLUSTER OF DIFFERENTIATION-1 ANTIGENS BY HUMAN CD4-CD8- CYTOLYTIC LYMPHOCYTES-T [J].
PORCELLI, S ;
BRENNER, MB ;
GREENSTEIN, JL ;
BALK, SP ;
TERHORST, C ;
BLEICHER, PA .
NATURE, 1989, 341 (6241) :447-450
[54]   CD1B RESTRICTS THE RESPONSE OF HUMAN CD4-8- LYMPHOCYTES-T TO A MICROBIAL ANTIGEN [J].
PORCELLI, S ;
MORITA, CT ;
BRENNER, MB .
NATURE, 1992, 360 (6404) :593-597
[55]  
PORCELLI SA, 1995, ADV IMMUNOL, V59, P1, DOI 10.1016/S0065-2776(08)60629-X
[56]   Glycolipid antigen processing for presentation by CD1d molecules [J].
Prigozy, TI ;
Naidenko, O ;
Qasba, P ;
Elewaut, D ;
Brossay, L ;
Khurana, A ;
Natori, T ;
Koezuka, Y ;
Kulkarni, A ;
Kronenberg, M .
SCIENCE, 2001, 291 (5504) :664-667
[57]   CD1d-restricted NK T cells are dispensable for specific antibody responses and protective immunity against liver stage malaria infection in mice [J].
Romero, JF ;
Eberl, G ;
Macdonald, HR ;
Corradin, G .
PARASITE IMMUNOLOGY, 2001, 23 (05) :267-269
[58]  
Rosat JP, 1999, J IMMUNOL, V162, P366
[59]   CD1d-restricted immunoglobulin G formation to GPI-anchored antigens mediated by NKT cells [J].
Schofield, L ;
McConville, MJ ;
Hansen, D ;
Campbell, AS ;
Fraser-Reid, B ;
Grusby, MJ ;
Tachado, SD .
SCIENCE, 1999, 283 (5399) :225-229
[60]  
Shamshiev A, 1999, EUR J IMMUNOL, V29, P1667, DOI 10.1002/(SICI)1521-4141(199905)29:05<1667::AID-IMMU1667>3.0.CO