scispace - formally typeset
X

Xiang-Yang Tan

Researcher at Pfizer

Publications -  28
Citations -  3140

Xiang-Yang Tan is an academic researcher from Pfizer. The author has contributed to research in topics: Receptor & RAGE (receptor). The author has an hindex of 13, co-authored 27 publications receiving 2947 citations.

Papers
More filters
Journal ArticleDOI

Interleukin (IL)-22 and IL-17 are coexpressed by Th17 cells and cooperatively enhance expression of antimicrobial peptides

TL;DR: IL-22 is identified as a new cytokine expressed by Th17 cells that synergizes with IL- 17A or IL-17F to regulate genes associated with skin innate immunity.
Journal ArticleDOI

Inhibition of the RAGE products increases survival in experimental models of severe sepsis and systemic infection

TL;DR: RAGE-/-, RAGE+/-, and anti-RAGE antibody-treated animals were resistant to lethality from Listeria monocytogenes by almost two orders of magnitude compared with wild-type mice and delayed treatment up to 24 hours after CLP resulted in a significant survival benefit compared with control mice.
Journal ArticleDOI

ADAMTS-8 exhibits aggrecanase activity and is expressed in human articular cartilage.

TL;DR: The ability of ADAMTS-8 to exhibit 'aggrecanase' activity was examined and a neoepitope monoclonal antibody was developed and used to demonstrate the ability of the protein to cleave aggrecan at the aggrecaase-susceptible Glu373-Ala374 peptide bond.
Journal ArticleDOI

Temporal associations between interleukin 22 and the extracellular domains of IL-22R and IL-10R2.

TL;DR: A temporal model for the development of a functional IL-22 cytokine-receptor-Fc complex is proposed, based on data studied, which indicates that the IL-10R2(ECD) binds to a surface created by the interaction between IL- 22 and the Il-22R(ECD), and thereby further stabilizes the association ofIL-22 within this cytokine/receptor complex.
Patent

Il-13 binding agents

TL;DR: In this paper, agents (i.e., antibodies and fragments thereof) that bind specifically to IL 13 and modulate the ability of IL 13 to interact with IL-13 receptors and signaling mediators are disclosed.