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The Cellular source and target of IL-21 in the K/BxN mouse model | 51142
Journal of Clinical and Cellular Immunology

Journal of Clinical and Cellular Immunology
Open Access

ISSN: 2155-9899

+44 1223 790975

The Cellular source and target of IL-21 in the K/BxN mouse model of rheumatoid arthritis


2nd International Conference on Clinical & Cellular Immunology

October 15-17, 2013 Hampton Inn Tropicana, Las Vegas, NV, USA

Haochu Huang

Scientific Tracks Abstracts: J Clin Cell Immunol

Abstract :

Cytokines are major regulators of immune responses. Particularly, IL-21 is a pluripotent cytokine that regulates B cell and plasma cell differentiation, and is thought to be an autocrine factor for T FH and T H 17 differentiation, two T cell subsets implicated in autoimmunity. The relevant cellular source and target cells of IL-21 in autoimmunity have not been well characterized. We investigated this issue in the K/BxN mice by comparing the ability to induce arthritis of wildtype KRN T cells, IL-21 knockout KRN T cells that cannot produce IL-21, IL-21 receptor knockout KRN T cells or B cells that cannot signal by IL-21, or ROR γ t knockout KRN T cells that are defective in Th17 differentiation. Our results showed that IL-21 production by T FH but not T H 17 T cells is critical for arthritis development. However, IL-21 does not act on T cells as an autocrine factor but rather acts on B cells to form germinal centers and produce autoantibodies. These results clarify the roles of IL-21 signaling to T cells or B cells in autoimmune diseases and have implications in developing effective therapies for rheumatoid arthritis and other antibody-mediated autoimmune diseases.

Biography :

Haochu Huang has completed his Ph.D. from Johns Hopkins University and postdoctoral studies in the lab of Drs. Christophe Benoist and Diane Mathis at Harvard Medical School. His work focuses on tolerance and regulation of autoreactive T cells and B cells in normal immune system and autoimmune diseases.

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