TLR8 seems to function differently in humans and mice. Until recently, TLR8 was believed to be nonfunctional in mice, but it seems to counteract TLR7 activity[2][3]
The TLR family plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen-associated molecular patterns (PAMPs) that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. The various TLRs exhibit different patterns of expression. This gene is predominantly expressed in lung and peripheral blood leukocytes, and lies in close proximity to another family member, TLR7, on chromosome X.[4]
TLR8 can recognize GU-rich single-stranded RNA.[5] However, the presence of GU-rich sequences in the single-stranded RNA is not sufficient to stimulate TLR8.[6] TLR8 recognizes G-rich oligonucleotides.[7]
TLR8 is an endosomal receptor that recognizes single stranded RNA (ssRNA), and can recognize ssRNA viruses such as Influenza, Sendai, and Coxsackie B viruses. TLR8 binding to the viral RNA recruits MyD88 and leads to activation of the transcription factor NF-κB and an antiviral response.[8] TLR8 recognizes single-stranded RNA of viruses such as HIV and HCV.[5][6]
TLR7 is functional both in human and mouse, but TLR8 is only functional in human.[3]
↑Peng G, Guo Z, Kiniwa Y, Voo KS, Peng W, Fu T, Wang DY, Li Y, Wang HY, Wang RF (August 2005). "Toll-like receptor 8-mediated reversal of CD4+ regulatory T cell function". Science. 309 (5739): 1380–4. Bibcode:2005Sci...309.1380P. doi:10.1126/science.1113401. PMID16123302.
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