CD1d-restricted immunoglobulin G formation to GPI-anchored antigens mediated by NKT cells

被引:332
作者
Schofield, L [1 ]
McConville, MJ
Hansen, D
Campbell, AS
Fraser-Reid, B
Grusby, MJ
Tachado, SD
机构
[1] Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
[2] Univ Melbourne, Dept Biochem & Mol Biol, Parkville, Vic 3052, Australia
[3] INSMED Pharmaceut, Richmond, VA 23219 USA
[4] Nat Prod & Glycotechnol, Durham, NC 27707 USA
[5] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[6] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
关键词
D O I
10.1126/science.283.5399.225
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Immunoglobulin G (IgG) responses require major histocompatibility complex (MHC)-restricted recognition of peptide fragments by conventional CD4(+) helper T cells. Immunoglobulin G responses to glycosylphosphatidylinositol (GPI)-anchored protein antigens, however, were found to be regulated in part through CD1d-restricted recognition of the GPI moiety by thymus-dependent, interleukin-4-producing CD4(+), natural killer cell antigen 1.1 [(NK1.1)(+)] helper T cells. The CD1-NKT cell pathway regulated immunogobulin G responses to the GPI-anchored surface antigens of Plasmodium and Trypanosoma and may be a general mechanism for rapid, MHC-unrestricted antibody responses to diverse pathogens.
引用
收藏
页码:225 / 229
页数:5
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