scispace - formally typeset
W

Weitao Huang

Researcher at LSU Health Sciences Center New Orleans

Publications -  20
Citations -  3241

Weitao Huang is an academic researcher from LSU Health Sciences Center New Orleans. The author has contributed to research in topics: Haematopoiesis & Proinflammatory cytokine. The author has an hindex of 11, co-authored 19 publications receiving 3115 citations. Previous affiliations of Weitao Huang include Louisiana State University.

Papers
More filters
Journal ArticleDOI

Requirement of Interleukin-17A for Systemic Anti-Candida albicans Host Defense in Mice

TL;DR: The data suggest that the mIL- 17A/mIL-17AR system is required for normal fungal host defense in vivo, and IL-17A could have potential as a therapeutic cytokine for systemic C. albicans infections in immunocompromised patients with cancer or advanced acquired immunodeficiency syndrome.
Journal Article

IL-17 Stimulates Granulopoiesis in Mice: Use of an Alternate, Novel Gene Therapy-Derived Method for In Vivo Evaluation of Cytokines

TL;DR: In this article, Adenovirus-mediated gene transfer of the murine IL-17 cDNA targeted to the liver (5 x 10(9) plaque-forming units (PFU) intravenous) resulted in a transiently transgenic phenotype, with dramatic effects on in vivo granulopoiesis.
Journal ArticleDOI

Requirement of endogenous stem cell factor and granulocyte-colony-stimulating factor for IL-17-mediated granulopoiesis.

TL;DR: There remained a significant SCF/G-CSF-independent effect of IL-17 on splenic granulopoiesis, resulting in a preservation of mature circulating granulocytes, which may have potential for therapeutic development.
Journal ArticleDOI

Requirement of IL-17 Receptor Signaling in Radiation-Resistant Cells in the Joint for Full Progression of Destructive Synovitis

TL;DR: It is reported that IL-17R signaling is required in radiation-resistant cells in the joint for full progression of chronic synovitis and bone erosion and chimeric mice of host IL- 17R−/− and donor wt BM cells were protected from chronic destructive arthritis similar to wt→wt chimeras.