AI Article Synopsis

  • The innate immune system uses pattern recognition receptors (PRRs) like Toll-like receptors (TLRs) to identify pathogens and trigger immune responses.
  • TLR7/8 are specific receptors that respond to viral RNA and bacterial DNA, leading to the release of proinflammatory cytokines and potential links to diseases like cancer and autoimmune disorders.
  • Research on TLR7/8 agonists and antagonists shows promise for immunotherapy, but challenges remain regarding their effectiveness and potential side effects.

Article Abstract

The innate immune system recognizes conserved features of viral and microbial pathogens through pattern recognition receptors (PRRs). Toll-like receptors (s) are one type of PRR used by the innate immune system to mediate the secretion of proinflammatory cytokines and promote innate and adaptive immune responses. family members 7 and TLR8 (referred to as 7/8 from herein) are endosomal transmembrane receptors that recognize purine-rich single-stranded RNA (ssRNA) and bacterial DNA, eliciting an immunologic reaction to pathogens. 7/8 were discovered to mediate the secretion of proinflammatory cytokines by activating immune cells. In addition, accumulating evidence has indicated that TLR7/8 may be closely related to numerous immune-mediated disorders, specifically several types of cancer, autoimmune disease, and viral disease. 7/8 agonists and antagonists, which are used as drugs or adjuvants, have been identified in preclinical studies and clinical trials as promising immune stimulators for the immunotherapy of these immune-mediated disorders. These results provided reasoning to further explore immunotherapy for the treatment of immune-mediated disorders. Nevertheless, numerous needs remain unmet, and the therapeutic effects of 7/8 agonists and antagonists are poor and exert strong immune-related toxicities. The present review aimed to provide an overview of the family members, particularly 7/8, and address the underlying molecular mechanisms and clinical implications of 7/8 in immune-mediated disorders. The aim of the work is to discuss the underlying molecular mechanisms and clinical implications of 7/8 in immune-mediated disorders.

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Source
http://dx.doi.org/10.1089/vim.2023.0077DOI Listing

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