Induction of a CD8(+) cytotoxic T lymphocyte response by cross-priming requires cognate CD4(+) T cell help

被引:613
作者
Bennett, SRM
Carbone, FR
Karamalis, F
Miller, JFAP
Heath, WR
机构
[1] PO ROYAL MELBOURNE HOSP, WALTER & ELIZA HALL INST MED RES, THYMUS BIOL UNIT, MELBOURNE, VIC 3050, AUSTRALIA
[2] ROYAL BRISBANE HOSP, QUEENSLAND INST MED RES, COOPERAT RES CTR VACCINE TECHNOL, HERSTON, QLD 4029, AUSTRALIA
[3] ALFRED HOSP, MONASH MED SCH, PRAHRAN, VIC 3181, AUSTRALIA
关键词
D O I
10.1084/jem.186.1.65
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Class I-restricted presentation is usually associated with cytoplasmic degradation of cellular proteins and is often considered inaccessible to exogenous antigens. Nonetheless, certain exogenous elements can gain entry into this so-called endogenous pathway by a mechanism termed cross-presentation. This is known to be effective for class I-restricted cytotoxic T lymphocyte (CTL) cross-priming directed against a variety of exogenous tumor, viral, and minor transplantation antigens. The related effect of cross-tolerance can also effectively eliminate responses to selected self components. In both cases, this presentation appears to require the active involvement of a bone marrow-derived antigen presenting cell (APC). Here, we show that CTL induction by cross-priming with cell-associated ovalbumin requires the active involvement of CD4(+) helper T cells. Importantly, this CD4(+) population is only effective when both the helper and CTL determinants are recognised on the same APC. Moreover, we would argue that the cognitive nature of this event suggests that the CD4(+) T cell actively modifies the APC, converting it into an effective stimulator for the successful priming of the CTL precursor.
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页码:65 / 70
页数:6
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