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David Leitenberg

Researcher at George Washington University

Publications -  21
Citations -  748

David Leitenberg is an academic researcher from George Washington University. The author has contributed to research in topics: T cell & ZAP70. The author has an hindex of 11, co-authored 21 publications receiving 699 citations. Previous affiliations of David Leitenberg include Children's National Medical Center & Washington University in St. Louis.

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CD45 modulates galectin-1-induced T cell death: regulation by expression of core 2 O-glycans.

TL;DR: It is determined that CD45 can positively and negatively regulate galectin-1-induced T cell death, depending on the glycosylation status of the cells, and oligosaccharide-mediated clustering of CD45 facilitated galECTin- 1-induced cell death.
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Integrated src kinase and costimulatory activity enhances signal transduction through single-chain chimeric receptors in T lymphocytes.

TL;DR: Comparing signaling characteristics of 9 single-chain receptors consisting of the H-2K(b) extracellular and transmembrane domains and various combinations of T cell signal transduction domains shows that it is possible to link TCR, coreceptor, and costimulatory activities in a single functional entity using modular domains.
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Novel Approach to Inhibit Asthma-Mediated Lung Inflammation Using Anti-CD147 Intervention

TL;DR: It is proposed that extracellular cyclophilins, via interaction with CD147, may contribute to the recruitment of leukocytes from the periphery into tissues during inflammatory responses, providing a novel mechanism whereby asthmatic lung inflammation may be reduced.
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A Secreted Protein from the Human Hookworm Necator americanus Binds Selectively to NK Cells and Induces IFN-γ Production

TL;DR: This work found that a protein(s) from ES products of adult N. americanus bound selectively to mouse and human NK cells, and this is the first report of a pathogen protein that binds exclusively to NK cells and the first reported of a nematode-derived product that induces abundant levels of cytokines from NK cells.
Journal Article

The TCR zeta-chain immunoreceptor tyrosine-based activation motifs are sufficient for the activation and differentiation of primary T lymphocytes.

TL;DR: The results show that the zeta-chain ITAMs, in the absence of the gamma, delta, and epsilon ITams, are sufficient for the activation and functional maturation of primary T lymphocytes, and supports the isolated use of the zetas in the development of surrogate TCRs for therapeutic purposes.