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Stephen D. Hurst

Researcher at Genentech

Publications -  28
Citations -  4857

Stephen D. Hurst is an academic researcher from Genentech. The author has contributed to research in topics: Cytokine & Antigen. The author has an hindex of 23, co-authored 27 publications receiving 4668 citations. Previous affiliations of Stephen D. Hurst include Northwestern University.

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IL-25 induces IL-4, IL-5, and IL-13 and Th2-associated pathologies in vivo.

TL;DR: The results suggest that IL-25, derived from Th2 T cells, is capable of amplifying allergic type inflammatory responses by its actions on other cell types.
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New IL-17 Family Members Promote Th1 or Th2 Responses in the Lung: In Vivo Function of the Novel Cytokine IL-25

TL;DR: The existence of a previously unrecognized cell population that may initiate Th2-like responses by responding to IL-25 in vivo is suggested and it is suggested thatIL-25 may be an important mediator of allergic disease via production of IL-4,IL-5, IL-13, and eotaxin.
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T cells that cannot respond to TGF-beta escape control by CD4(+)CD25(+) regulatory T cells.

TL;DR: It is shown that CD4+CD25+ T reg cells from the thymus of dnTβRII mice retain the ability to inhibit colitis, suggesting that T cell responsiveness to TGF-β is not required for the development or peripheral function of thymic-derived TReg cells.
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Differential CC chemokine-induced enhancement of T helper cell cytokine production.

TL;DR: Results suggest CC chemokines play a role in regulating naive Th cell cytokine production, in addition to regulating leukocyte trafficking.
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IL-25 regulates Th17 function in autoimmune inflammation

TL;DR: It is shown that IL-25 also regulates the development of autoimmune inflammation mediated by IL-17–producing T cells, and plays opposing roles in the pathogenesis of organ-specific autoimmunity.