IL-10 welectively regulates murine Ig isotype switching
スポンサーリンク
概要
著者
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Stuber Eckhard
Laboratory Of Clinical Investigation National Institutes Of Health
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Snapper Clifford
Department Of Pathology Usuhs
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Snapper Clifford
Pathology Uniformed Services University Department Of The Health Sciences
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MOND James
Departments of Medicine Pathology Uniformed Services University of the Health Sciences
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JIN Liang
Departments of Pathology Uniformed Services University of the Health Sciences
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KEHRY Marilyn
Boehringer-lngelheim Pharmaceuticals
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SHPARAGO Neil
Walter Reed Army Medical Center
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ZELAZOWSKI Piotr
Department of Pathology USUHS
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MCLNTYRE Tina
Department of Pathology USUHS
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PECANHA Ligia
Depto de Imunologia-IM-UFRJ
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MAX Edward
Center for Biologics, Evaluation, and Research, Food and Drug Administration
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Jin Liang
Department Of Pathology Usuhs
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Max Edward
Center For Biologics Evaluation And Research Food And Drug Administration
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Mond J
Departments Of Medicine Pathology Uniformed Services University Of The Health Sciences
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Kehry Marilyn
Boehringer-ingelheim Pharmaceuticals Inc.
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Mond James
Department Of Medicine
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KEHRY Marilyn
Boehringer Ingelheim Pharmaceuticals Inc.
関連論文
- T Versus T cytokine profile determines the modulation of in vitro T Cell-independent type 2 responses by IL-4
- Multivalent cross-linking of membrane lg sensitizes murine Bcells to a broader spectrum of CpG-containing oligodeoynucleotide motifs, including their methylated counterparts, for stimulation of proliferation and lg secretion
- IFN-γ is a potent inducer of lg secretion by sort-purified murine B cells activated through the mlg, but not the CD40, signaling pathway
- IL-10 welectively regulates murine Ig isotype switching
- Interaction of B cells with activated T cells reduces the threshold for CD40-mediated B cell activation
- Phenotypic and functional characterization of a panel of cytotoxic murine NK cell clones that are heterogeneous in their enhancement of lg secretion in vitro
- Heterogeneity in the ability of cytotoxic murine NK cell clones to enhance lg secretion in vitro