Toll-Like Receptor 8-Mediated Reversal of CD4 + Regulatory T Cell Function

Author:

Peng Guangyong1,Guo Zhong1,Kiniwa Yukiko1,Voo Kui shin1,Peng Weiyi1,Fu Tihui1,Wang Daniel Y.1,Li Yanchun1,Wang Helen Y.1,Wang Rong-Fu1

Affiliation:

1. The Center for Cell and Gene Therapy and Department of Immunology, Baylor College of Medicine, Houston, TX 77030, USA.

Abstract

CD4 + regulatory T (Treg) cells have a profound ability to suppress host immune responses, yet little is understood about how these cells are regulated. We describe a mechanism linking Toll-like receptor (TLR) 8 signaling to the control of Treg cell function, in which synthetic and natural ligands for human TLR8 can reverse Treg cell function. This effect was independent of dendritic cells but required functional TLR8-MyD88-IRAK4 signaling in Treg cells. Adoptive transfer of TLR8 ligand-stimulated Treg cells into tumor-bearing mice enhanced anti-tumor immunity. These results suggest that TLR8 signaling could play a critical role in controlling immune responses to cancer and other diseases.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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