The study shows how the protein called polyglutamine-binding protein 1 (PQBP1) acts as a front-line sensor and is critical to initiating an immune response to HIV.
When the PQBP1 encounters the virus, it starts a programme that triggers an overall protective environment against infection and enhances the production of virus-specific antibodies.
"Vaccines work by teaching the immune system to react by mimicking a natural infection," said lead author Sunnie Yoh, a postdoctoral fellow in the lab of Sumit Chanda, director of the Immunity and Pathogenesis Programme at Sanford-Burnham Medical Research Institute.
"Current approaches to HIV vaccine development have thus far yielded little fruit, partly because of the lack of an effective vaccine adjuvant. Adjuvants promote a robust immune response to vaccines and are critical to eliciting long-lasting immunity," said Chanda.
"Our study identifies a promising new target for a vaccine adjuvant that could advance the development of HIV vaccines and prevent infection," Chanda said.
Although the major target of HIV infection is CD4+ T cells, dendritic cells are one of the first cell types to encounter HIV during sexual transmission.
Dendritic cells control the innate immune response - a generic, non-specific defence against pathogens.
These cells also activate the adaptive immune response that generates highly specific antibodies that provide protective, long-lasting immunity.
Both the innate and adaptive immune systems are necessary to provide an optimal immune response to vaccines.
"PQBP1 acts as a sentry for innate immune response to HIV. The development of a highly effective HIV vaccine will likely depend on both combining the correct immunogens, which are viral proteins, and unlocking the innate response, to establish long-lived protection," said Chanda.
The research was published in the journal Cell.
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