The activation, differentiation, and subsequent effector functions of CD4 T cells depend on interactions with a multitude of MHC class II (MHCII)-expressing APCs. To evaluate the individual contribution of various APCs to CD4 T cell function, we have designed a new murine tool for selective in vivo expression of MHCII in subsets of APCs. Conditional expression of MHCII in B cells was achieved using a cre-loxP approach. After i.v. or s.c. priming, partial proliferation and activation of CD4 T cells was observed in mice expressing MHCII only by B cells. Restricting MHCII expression to B cells constrained secondary CD4 T cell responses in vivo, as demonstrated in a CD4 T cell-dependent model of autoimmunity, experimental autoimmune encephalomyelitis. These results highlight the limitations of B cell Ag presentation during initiation and propagation of CD4 T cell function in vivo using a novel system to study individual APCs by the conditional expression of MHCII.
Cutting edge: Conditional MHC class II expression reveals a limited role for B cell antigen presentation in primary and secondary CD4 T cell responses.
前沿研究:条件性 MHC II 类表达揭示了 B 细胞抗原呈递在初级和次级 CD4 T 细胞反应中的作用有限
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| 期刊: | Journal of Immunology | 影响因子: | 3.400 |
| 时间: | 2013 | 起止号: | 2013 Jul 15; 191(2):545-50 |
| doi: | 10.4049/jimmunol.1201598 | 研究方向: | 细胞生物学 |
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