CD30-MEDIATED SIGNALING PROMOTES THE DEVELOPMENT OF HUMAN T-HELPER TYPE 2-LIKE T-CELLS

被引:148
作者
DELPRETE, G
DECARLI, M
DELIOS, MM
DANIEL, KC
ALMERIGOGNA, F
ALDERSON, M
SMITH, CA
THOMAS, E
ROMAGNANI, S
机构
[1] UNIV FLORENCE, DIV CLIN IMMUNOL & ALLERGY, I-50134 FLORENCE, ITALY
[2] UNIV PISA, INST INTERNAL MED, I-56100 PISA, ITALY
[3] IMMUNEX RES & DEV CORP, SEATTLE, WA 98101 USA
关键词
D O I
10.1084/jem.182.6.1655
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have recently shown that CD30, a member of the tumor necrosis factor/nerve growth factor receptor superfamily, is preferentially expressed by human T cell clones producing T helper (Th) type 2 cytokines. We report here that costimulation with an agonistic anti-CD30 monoclonal antibody enhanced antigen (Ag)-induced proliferation and cytokine secretion by established human Th2 and Th0 clones. Moreover, costimulation of peripheral blood mononuclear cells with the same anti-CD30 monoclonal antibody resulted in the preferential development of Ag-specific T cell lines and clones showing a Th2-like profile of cytokine secretion. In contrast, early blockade III bulk culture of CD30 ligand-CD30 interaction shifted the development of Ag-specific T cells towards the opposite (Th1-like) phenotype. Taken together, these data suggest that CD30 triggering of activated Th cells by CD30 ligand-expressing Ag-presenting cells may represent an important costimulatory signaling for the development of Th2-type responses.
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收藏
页码:1655 / 1661
页数:7
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