Dendritic cells genetically modified to express CD40 ligand and pulsed with antigen can initiate antigen-specific humoral immunity independent of CD4+ T cells

被引:68
作者
Kikuchi, T
Worgall, S
Singh, R
Moore, MAS
Crystal, RG [1 ]
机构
[1] Cornell Univ, Weill Med Coll, Dept Med, Div Pulm & Crit Care Med, New York, NY 10021 USA
[2] Cornell Univ, Weill Med Coll, Dept Pediat, New York, NY USA
[3] Cornell Univ, Weill Med Coll, Belfer Gene Therapy Core Facil, New York, NY USA
[4] Cornell Univ, Weill Med Coll, Inst Med Genet, New York, NY USA
[5] Mem Sloan Kettering Canc Ctr, James Ewing Lab Dev Hematopoiesis, New York, NY 10021 USA
关键词
D O I
10.1038/80498
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have investigated whether dendritic cells genetically modified to express CD40 ligand and pulsed with antigen can trigger B cells to produce antigen-specific antibodies without CD4(+) T-cell help. Dendritic cells modified with a recombinant adenovirus vector to express CD40 ligand and pulsed with heat-killed Pseudomonas induced naive B cells to produce antibodies against Pseudomonas in the absence of CD4(+) T cells in vitro, initiated Pseudomonas-specific humoral immune responses in vivo in wild-type and CD4(-/-) mice, and protected immunized wild-type and CD4(-/-), but not B-cell(-/-) mice, from lethal intrapulmonary challenge with Pseudomonas. Thus, genetic modification of dendritic cells with CD40 ligand enables them to present a complex mixture of microbial antigens and establish CD4(+) T cell-independent, B cell-mediated protective immunity against a specific microbe.
引用
收藏
页码:1154 / 1159
页数:6
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