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

Article Abstract:

Research demonstrates that dendritic cells with CD40 ligand when primed with heat-killed Pseudomonas, express B cells against Pseudomonas in the absence of CD4+ T cells. Data show that the cells exhibit pseudomonas-specific humoral immune response in wild-type mice lacking CD4 but not in B-cell lacking mice.

Author: Kikuchi, Toshiaki, Worgall, Stefan, Singh Ravi, Moore, Malcolm A.S., Crystal, Ronald G.
Publisher: Nature America, Inc.
Publication Name: Nature Medicine
Subject: Health
ISSN: 1078-8956
Year: 2000
Analysis, Physiological aspects, Pseudomonas, Immunity, Immunity (Physiology), T cells, Immune response, Antigen presenting cells, CD4 lymphocytes, Immune response regulation

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Impaired recruitment of bone-marrow-derived endothelial and hematopoietic precursor cells blocks tumor angiogenesis and growth

Article Abstract:

Research presented concerns the association between bone marrow-derived precursor cells and tumor angiogenesis. Findings suggest that recruitment of vascular endothelial growth factor bone marrow-derived cells promotes tumor angiogenesis, thus blocking these cells may have implications for halting tumor growth.

Author: Moore, Malcolm A.S., Crystal, Ronald G., Benezra, Robert, Wu, Yan, Lyden, David, Hattori, Koichi, Dias, Sergio, Costa, Carla, Blaikie, Pamela, Butros, Linda, Chadburn, Amy, Heissig, Beate, Marks, Willy, Witte, Larry, Hicklin, Daniel, Zhu, Zhenping, Hackett, Neil R., Hajjar, Katherine A., Manova, Katia, Rafii, Shahin
Publisher: Nature America, Inc.
Publication Name: Nature Medicine
Subject: Health
ISSN: 1078-8956
Year: 2001
Statistical Data Included, Growth, Neovascularization, B cells, Vascular endothelial growth factor, Tumors

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Trans-splicing repair of CD40 ligand deficiency results in naturally regulated correction of a mouse model of hyper-IgM X-linked immunodeficiency

Article Abstract:

A study was conducted to demonstrate the use of trans-splicing to correct the CD40L mutation while preserving the natural regulation and cell specificity of CD40L expression in a mouse CD40L-knockout model. The result confirms the use of CD40L trans-splicing to correct hyper-IgM (HIGM1), leading to functional correction of the genetic defect without the adverse consequences of unregulated expression of the CD40L gene.

Author: Crystal, Ronald G., Lesser, Martin L., Tahara, Minoru, Pergolizzi, Robert G., Kobayashi, Hiroyasu, Krause, Anja, Luettich, Karsta
Publisher: Nature America, Inc.
Publication Name: Nature Medicine
Subject: Health
ISSN: 1078-8956
Year: 2004
Science & research, Gene mutations, Gene mutation, Gene expression

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Subjects list: United States, Research
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