4.8 Article

Coagulation Factor X Activates Innate Immunity to Human Species C Adenovirus

Journal

SCIENCE
Volume 338, Issue 6108, Pages 795-798

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1226625

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Funding

  1. U.S. NIH [AI065429, CA141439]
  2. University of Washington National Institute of Environmental Health Sciences [P30ES07033]
  3. Washington State Life Sciences Discovery Fund
  4. Center for Intracellular Delivery of Biologics Analytical Biopharmacy Core facility

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Although coagulation factors play a role in host defense for living fossils such as horseshoe crabs, the role of the coagulation system in immunity in higher organisms remains unclear. We modeled the interface of human species C adenovirus (HAdv) interaction with coagulation factor X (FX) and introduced a mutation that abrogated formation of the HAdv-FX complex. In vivo genome-wide transcriptional profiling revealed that FX-binding-ablated virus failed to activate a distinct network of nuclear factor kappa B-dependent early-response genes that are activated by HAdv-FX complex downstream of TLR4/MyD88/TRIF/TRAF6 signaling. Our study implicates host factor decoration of the virus as a mechanism to trigger an innate immune sensor that responds to a misplacement of coagulation FX from the blood into intracellular macrophage compartments upon virus entry into the cell.

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