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Erwin W. Gelfand

Researcher at University of Colorado Denver

Publications -  679
Citations -  37565

Erwin W. Gelfand is an academic researcher from University of Colorado Denver. The author has contributed to research in topics: Immunoglobulin E & T cell. The author has an hindex of 99, co-authored 675 publications receiving 36059 citations. Previous affiliations of Erwin W. Gelfand include University of Colorado Hospital & University of Virginia.

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Journal Article

Antibody-mediated target cell lysis by nonimmune cells: the use of anti-immunoglobulin to distinguish effector cell population.

TL;DR: The role of a goat IgG anti-rabbit immunoglobulin on antibody-mediated target cell lysis by nonimmune cells was investigated and the mechanism of enhancement appeared to be due to cross-linking between effector lymphocytes and antibody-coated target cells by the divalent anti-immunoglOBulin.
Journal Article

Heterogeneity of Human Thymocytes and a Malignant T-Lymphoblast Cell Line, MOLT-3

TL;DR: Analysis of the subpopulations of thymocytes demonstrated that they represent a heterogeneous population of cells with respect to their size, proliferative activity, and presence and quantities of terminal deoxynucleotidyl transferase and human thymus leukemia-associated antigen, a thymic isozyme of adenosine deaminase.
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Safety and tolerability of increased rate of infusion of intravenous immunoglobulin G, 10% in antibody-deficient patients.

TL;DR: Increasing the rate of infusion of IGIV-C, 10% by 75% up to 0.14 mL/kg/min (840 mg/ kg/h) was well tolerated, suggesting safe administration of IGiva, 10%, at this rate, and resulted in a shortened overall infusion time.
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A prostacyclin agonist with thromboxane inhibitory activity for airway allergic inflammation in mice.

TL;DR: The effect of ONO‐1301 on development of airway allergic inflammation is investigated and it is shown that the drug acts as a prostacyclin agonist with thromboxane A2 synthase inhibitory activity.
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Pretreatment with allergen prevents immediate hypersensitivity and airway hyperresponsiveness.

TL;DR: The data suggest that IgE (and IgG1) responses and airway hyperresponsiveness induced by allergen sensitization via the airways can be modulated by subcutaneous administration of peptide.