Abstract
Heat shock proteins interact with antigen-presenting cells through their receptor, CD91, eliciting a cascade of events including maturation, activation and representation of chaperoned foreign peptides with class I molecules on their surface. In turn, this facilitates recognition of non-self leading to induction of a cytotoxic T cell response. The abundance of heat shock proteins in tumours and their presence in virion coats makes them attractive propositions for use in antitumour and antiviral strategies.
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Stebbing, J., Savage, P., Patterson, S., & Gazzard, B. (2004). All for CD91 and CD91 for all. Journal of Antimicrobial Chemotherapy, 53(1), 1–3. https://doi.org/10.1093/jac/dkh010
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