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Generation of tumor-associated cytotoxic T lymphocytes requires interleukin 4 from CD8+ T cells
被引:55
作者:
Schüler, T
Kammertoens, T
Preiss, S
Debs, P
Noben-Trauth, N
Blankenstein, T
机构:
[1] Free Univ Berlin, Inst Immunol, D-12200 Berlin, Germany
[2] NIH, Immunol Lab, Rockville, MD 20582 USA
[3] Max Delbruck Ctr Mol Med, D-13092 Berlin, Germany
关键词:
tumor vaccination;
cytotoxic T lymphocytes;
interleukin;
4;
interleukin 4 (receptor)-deficient mice;
cross-priming;
D O I:
10.1084/jem.194.12.1767
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Activation of tumor-associated CD8(+) cytotoxic T lymphocytes (CTLs) often requires antigen representation, e.g., by dendritic cells (DCs), and CD4(+) T cell help. Previously, we showed that CTL-mediated tumor immunity required interleukin 4 (IL-4) during the immunization but not effector phase. To determine the source and target cells of IL-4, we performed adoptive T cell transfers using CD4(+) and CD8(+) T cells from IL-4(-/-) and IL-4R(-/-) mice and analyzed CTL generation. Even though necessary for CTL generation, CD4(+). T cells did not need to express IL-4 or IL-4R. Surprisingly, CTL generation required IL-4 but not IL-4R expression by CD8(+) T cells. As IL-4 (a) was expressed by naive CD8(+) T cells within 24 h after antigen encounter, (b) IL-4 induced DC maturation, and (c) CTL development was impaired in T cell-reconstituted IL-4P(-/-) mice, CD8(+) T cell-derived IL-4 appears to act on DCs. We conclude that CD4(+) and CD8(+) T cells provide different signals for DC activation during CTL generation.
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页码:1767 / 1775
页数:9
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