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Hachiro Senoh

Researcher at Osaka University

Publications -  10
Citations -  949

Hachiro Senoh is an academic researcher from Osaka University. The author has contributed to research in topics: Antibody & Proinflammatory cytokine. The author has an hindex of 7, co-authored 10 publications receiving 934 citations.

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T cell activation-associated hepatic injury: mediation by tumor necrosis factors and protection by interleukin 6.

TL;DR: TNFs are critical cytokines for inducing T cell activation-associated (Con A-induced) hepatitis and the induction of hepatitis is almost completely controlled by rIL-6, which exerts its protective effect through multiple mechanisms including the reduction of TNF production.
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Critical involvement of interferon gamma in the pathogenesis of T-cell activation-associated hepatitis and regulatory mechanisms of interleukin-6 for the manifestations of hepatitis.

TL;DR: Results indicate that IFN‐γ plays a critical role in the development of Con A‐induced acute hepatitis and suggest that IL‐6 administration can regulate the manifestation of hepatitis through mechanisms including the reduced production of inflammatory cytokines such as IFN-γ.
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Enhanced production of interleukin-6 in mice with type II collagen-induced arthritis.

TL;DR: An interleukin-6 (IL-6)-dependent cell line from murine plasmacytoma MOPC-104E cells was found to respond to murine and to human IL-6, but not to any other cytokines, and it is found that the L3T4+ T cell subset is responsible for the enhanced production of IL- 6 in arthritic mice.
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Studies on Anti-inflammatory Agents. IV. Synthesis and Pharmacological Properties of 1, 5-Diarylpyrazoles and Related Derivatives

TL;DR: A series of novel 1,5-diarylpyrazole derivatives was synthesized and tested for anti-inflammatory and analgesic activities to develop anti- inflammatory agents with fewer side effects than existing nonsteroidal anti- inflammation drugs.
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Strain difference in the induction of T-cell activation–associated, interferon gamma–dependent hepatic injury in mice

TL;DR: Results indicate that, while IFN‐γ produced in vivo by activated T cells induces hepatic injury, there exists a striking strain difference in the induction of IFN-γ–dependent hepatic Injury.