Th2-dependent B cell responses in the absence of CD40-CD40 ligand interactions

被引:17
作者
Chirmule, N
Tazelaar, J
Wilson, JM
机构
[1] Univ Penn, Inst Human Gene Therapy, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Mol & Cellular Engn, Philadelphia, PA 19104 USA
[3] Wistar Inst Anat & Biol, Dept Mol & Cellular Engn, Philadelphia, PA 19104 USA
关键词
D O I
10.4049/jimmunol.164.1.248
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD40 is thought to play a central role in T cell-dependent humoral responses through two distinct mechanisms. CD4(+) T helper cells are activated via CD40-dependent Ag presentation in which CD80/CD86 pro,ides costimulation through CD28, In addition, engagement of CD40 on B cells provides a direct pathway for activation of humoral responses, We used a model of adenovirus-mediated gene transfer of beta-galactosidase (lacZ) into murine lung to evaluate the specific CD40-dependent pathways required for humoral immunity at mucosal surfaces of the lung. Animals deficient in CD40L failed to develop T and B cell responses to vector. Activation of Th2 cells, which normally requires CD40-dependent stimulation of APCs, was selectively reconstituted in CD40 ligand-deficient mice by systemic administration of an Ab that is agonistic to CD28, Surprisingly, this resulted in the development of a functional humoral response to vector as evidenced by formation of germinal centers and production of antiadenovirus IgG1 and IgA that neutralized and prevented effective readministration of vector. The CD28-dependent B cell response required CD4(+) T cells and was mediated via IL-4, These studies indicate that CD40 signals to the B cells are not necessary for CD4(+) Th2 cell-dependent humoral responses to be generated.
引用
收藏
页码:248 / 255
页数:8
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