scispace - formally typeset
J

Joost J. Oppenheim

Researcher at National Institutes of Health

Publications -  463
Citations -  61853

Joost J. Oppenheim is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Chemokine & Interleukin. The author has an hindex of 130, co-authored 454 publications receiving 59601 citations. Previous affiliations of Joost J. Oppenheim include Science Applications International Corporation & University of Birmingham.

Papers
More filters
Journal ArticleDOI

Properties of the Novel Proinflammatory Supergene "Intercrine" Cytokine Family

TL;DR: This review has summarized and discussed the available information concerning the regulation and structure of the genes, the structure and biochemical properties of the polypeptide products, their receptors, signal transduction, cell sources, and in vitro as well as in vivo activities of these cytokines.
Journal Article

International Union of Pharmacology. XXII. Nomenclature for Chemokine Receptors

TL;DR: A widely accepted receptor nomenclature system is described, ratified by the International Union of Pharmacology, that is facilitating clear communication in this area and updating current concepts of the biology and pharmacology of the chemokine system.
Journal ArticleDOI

β-Defensins: Linking Innate and Adaptive Immunity Through Dendritic and T Cell CCR6

TL;DR: In this paper, human β-defensin was selectively chemotactic for cells stably transfected to express human CCR6, a chemokine receptor preferentially expressed by immature dendritic cells and memory T cells.
Journal ArticleDOI

There is more than one interleukin 1.

TL;DR: The biochemical characteristics, gene cloning, cell sources, biological properties and actions of IL-1 are discussed, and reasons why this pleitotropic, nonspecific hormone-like cytokine is of considerable concern to immunologists are given.
Journal ArticleDOI

Ll-37, the Neutrophil Granule–And Epithelial Cell–Derived Cathelicidin, Utilizes Formyl Peptide Receptor–Like 1 (Fprl1) as a Receptor to Chemoattract Human Peripheral Blood Neutrophils, Monocytes, and T Cells

TL;DR: The results suggest that, in addition to its microbicidal activity, LL-37 may contribute to innate and adaptive immunity by recruiting neutrophils, monocytes, and T cells to sites of microbial invasion by interacting with FPRL1.