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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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Loss of T Regulatory Cell Suppression following Signaling through Glucocorticoid-induced Tumor Necrosis Receptor (GITR) Is Dependent on c-Jun N-terminal Kinase Activation

TL;DR: Treatment with an inhibitor of JNK phosphorylation resulted in complete reversal of all GITR-induced changes in nTreg phenotype and function, with full restoration of suppression of in vivo lung allergic responses and in vitro proliferation of activated CD4+CD25− T cells.
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Platelet-activating factor enhances Ig production in B lymphoblastoid cell lines.

TL;DR: Data indicate that PAF may have an important immunomodulatory role in the production of Ig by B lymphocytes, and an ELISA spot assay for enumeration of Ig-secreting cells demonstrated that the increase in Ig production is likely due to enhancement of single cell Ig secretion rather than an increase in cell number.
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Functional differentiation of B lymphocytes in congenital agammaglobulinemia. I. Generation of hemolytic plaque-forming cells.

TL;DR: Findings indicate the presence of B lymphocyte precursors in the majority of patients with cAgamma investigated, and specifically a specific hemolytic plaque-forming cell response in vitro to sheep red blood cells and ovalbumin.
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Disseminated Legionella pneumophila infection in an infant with severe combined immunodeficiency

TL;DR: A case of fatal Legionnaire disease is reported in an infant with severe combined immunodeficiency who developed disseminated infection involving the lungs, liver, and brain.
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Calcium-induced ERK activation in human T lymphocytes

TL;DR: The activation of ERK1 and 2 by calcium ionophores was rapid, transient, and occurred in a dose-dependent manner in human primary and Jurkat T lymphocytes as mentioned in this paper.