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Abrams John S

Researcher at University of Wisconsin-Madison

Publications -  15
Citations -  1637

Abrams John S is an academic researcher from University of Wisconsin-Madison. The author has contributed to research in topics: Monoclonal antibody & Eosinophil. The author has an hindex of 8, co-authored 15 publications receiving 1605 citations.

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Strategies of anti-cytokine monoclonal antibody development: immunoassay of IL-10 and IL-5 in clinical samples.

TL;DR: The general strategy for preparing a large panel of anti-mouse and human cytokine monoclonal antibodies (mAb) and setting up cytokine immunoassays and this review outlines the general strategy followed.
Journal Article

APCs Express DCIR, a Novel C-Type Lectin Surface Receptor Containing an Immunoreceptor Tyrosine-Based Inhibitory Motif

TL;DR: DCIR represents a novel surface molecule expressed by Ag presenting cells, and of potential importance in regulation of DC function, and was expressed on DC, monocytes, macrophages, B lymphocytes, and granulocytes, but not detected on NK and T cells.
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Immediate and late airway response of allergic rhinitis patients to segmental antigen challenge. Characterization of eosinophil and mast cell mediators.

TL;DR: It is suggested that eosinophils are attracted to the airway during the late-phase allergic reaction and that IL-5 may produce changes in airway eos inophil density and promote the release of granular proteins to cause airway injury.
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Interleukin‐6 Production by Schwann Cells and Induction in Sciatic Nerve Injury

TL;DR: In vitro data demonstrate that iSC cells produce IL‐6 in response to PC12 cell coculture and to stimuli that induce IL‐8 production in the hematopoietic lineage and the induction of IL‐ 6 message distal to a crush injury suggests another mechanism by which Schwann cells facilitate peripheral nerve regeneration.
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Differential regulation of IL-13 and IL-4 production by human CD8+ and CD4+ Th0, Th1 and Th2 T cell clones and EBV-transformed B cells

TL;DR: The results indicate that the differences in expression and biological activities of IL-4 and IL-13 on T cells may have consequences for the relative roles of these cytokines in the immune response.