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Charles A. Dinarello

Researcher at University of Colorado Denver

Publications -  1073
Citations -  152254

Charles A. Dinarello is an academic researcher from University of Colorado Denver. The author has contributed to research in topics: Interleukin & Cytokine. The author has an hindex of 190, co-authored 1058 publications receiving 139668 citations. Previous affiliations of Charles A. Dinarello include University of Guadalajara & Pennsylvania State University.

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Journal ArticleDOI

IL-32gamma and Streptococcus pyogenes cell wall fragments synergise for IL-1-dependent destructive arthritis via upregulation of TLR-2 and NOD2.

TL;DR: It is shown that IL-32γ aggravates SCW-induced arthritis by the upregulation of TLR-2/NOD2 expression and promotes severe joint erosion in an IL-1-dependent fashion.
Patent

Human il-1 cDNA sequences encoding biologically-active human il-1 proteins

TL;DR: In this paper, the truncated human IL-1 cDNA sequences of the subject invention are contained in specified plasmids whose constructions are described in detail, and they are useful to induce the production of IL-2 by activated T-cells.
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GM-CSF DNA induces specific patterns of cytokines and chemokines in the skin: implications for DNA vaccines.

TL;DR: Early events following GM-CSF DNA administration were characterized by high levels of inflammatory molecules, later followed by expression of precursor Th1 cytokines, IL-12 and IL-18, concomitant with IFNgamma production, which provided a basis for development of new approaches to cancer vaccines, including the use of cytokine genes as adjuvants.
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Characterization of Limulus amoebocyte lysate-reactive material from hollow-fiber dialyzers.

TL;DR: Results indicate that the Limulus amoebocyte lysate reactive material is cellulose derived and not pyrogenic.
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Soluble human p55 and p75 tumor necrosis factor receptors reverse spontaneous arthritis in transgenic mice expressing transmembrane tumor necrosis factor α

TL;DR: These data show that arthritis is sufficiently initiated and maintained in tmTNFalpha-transgenic/T NFalpha-KO mice, and that it can be neutralized by recombinant human p55 or p75 sTNFR, resulting in amelioration of the biologic and subsequent histologic destructive effects of tm TNFalpha.