Down modulation of human TLR3 function by a monoclonal antibody.

DUFFY KE, LAMB RJ, SAN MATEO LR, JORDAN JL, CANZIANI G, BRIGHAM-BURKE M, KORTEWEG J, CUNNINGHAM M, BECK HS, CARTON J, GILES-KOMAR J, DUCHALA C, SARISKY RT, MBOW ML.

CELLULAR IMMUNOLOGY

ACADEMIC PRESS INC ELSEVIER SCIENCE

Año: 2007 vol. 248 p. 103 - 114

0008-8749

Toll-like receptors are a family of pattern-recognition receptors that contribute to the innate immune response. Toll-like receptor 3 (TLR3) signals in response to foreign, endogenous and synthetic ligands including viral dsRNA, bacterial RNA, mitochondrial RNA, endogenous necrotic cell mRNA and the synthetic dsRNA analog, poly(I:C). We have generated a monoclonal antibody (mAb CNTO2424) that recognizes the extracellular domain (ECD) of human TLR3 in a conformation-dependent manner. CNTO2424 down-regulates poly(I:C)-induced production of IL-6, IL-8, MCP-1, RANTES, and IP-10 in human lung epithelial cells. In addition, mAb CNTO2424 was able to interfere with the known TLR3-dependent signaling pathways, namely NF-kappaB, IRF-3/ISRE, and p38 MAPK. The generation of this neutralizing anti-TLR3 mAb provides a unique tool to better understand TLR3 signaling and potential cross-talk between TLR3 and other molecules.