The lgV domain of human B7-2 (CD86) is sufficient to co-stimulate T lymphocytes and induce cytokine secretion
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概要
著者
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Greenfield Edward
Departments Of Molecular Biology And Immunology Repligen Corp.
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Levine Bruce
Immune Cell Biology Program Naval Medical Research Institute
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Ueda Yuji
Immune Cell Biology Program Naval Medical Research Institute
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Freeman Gordon
Division Of Hematologic Malignancies Dana-farber Cancer Institute Harvard Medical School
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RENNERT Paul
Departments of Molecular Biology and Immunology, Repligen Corp.
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FURLONG Kimberly
Departments of Molecular Biology and Immunology, Repligen Corp.
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JELLIS Cindy
Departments of Molecular Biology and Immunology, Repligen Corp.
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JUNE Carl
Immune Cell Biology Program, Naval Medical Research Institute
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GRAY Gary
Departments of Molecular Biology and Immunology, Repligen Corp.
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Gray Gary
Departments Of Molecular Biology And Immunology Repligen Corp.
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June Carl
Immune Cell Biology Program Naval Medical Research Institute
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Jellis Cindy
Departments Of Molecular Biology And Immunology Repligen Corp.
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Rennert Paul
Departments Of Molecular Biology And Immunology Repligen Corp.
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Rennert Paul
Department Of Immunology/inflammation Biogen Inc.
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Furlong Kimberly
Departments Of Molecular Biology And Immunology Repligen Corp.
関連論文
- The lgV domain of human B7-2 (CD86) is sufficient to co-stimulate T lymphocytes and induce cytokine secretion
- Both CD28 ligands CD80(B7-1) and CD86(B7-2) activate phosphatidylinositol 3-kinase, and wortmannin reveals heterogeneity in the regulation of T cell IL-2 secretion
- CD28 ligands CD80(B7-1) and CD86(B7-2) induce long-term autocrine growth of CD4+T cells and induce similar patterns of cytokine secretion in vitro
- Primary porcine endothelial cells express membrane-bound B7-2 (CD86) and a soluble factor that co-stimulate cyclosporin A-resistant and CD28-dependent human T cell proliferation
- Selective desruption of lymphotoxin ligands reveals a novel set of mucosal lymph nodes and unique effects on lymph node cellular organization