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Single Birth Gene Therapy Yields Years-Long HIV Protection in Primates

AUSTRALIA, JUL 30 – Researchers found CD8 T-cell responses to conserved HIV peptides may help control viral rebound during treatment interruptions in 68 men with HIV, suggesting new vaccine targets.

  • At the International AIDS Society Conference on HIV Science, data showed that IMAP-peptides were detected in 52%-100% of rebound HIV-1 sequences from participants in the PULSE trial of 68 men who have sex with men living with HIV.
  • The IMAP analysis pipeline selected 182 peptides from structurally important and mutation-intolerant HIV-1 regions, building on prior findings linking CD8 T-cell responses to five conserved HIV regions.
  • Among four noncontrollers and five transient controllers, IMAP-peptides appeared in 52%-100% of viral sequences across three ATIs, with CD8 T-cells showing a 15- to 53-fold higher effector response in transient controllers.
  • The results underscore IMAP’s potential for informing new treatment strategies, prompting efforts to develop and test mRNA vaccine constructs containing IMAP-peptides to assess immune responses in people living with HIV.
  • Looking ahead, the IMAP technique could be applied to other viruses, with future studies testing mRNA vaccine constructs in a humanized mouse model.
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Novel Peptides Expressed in HIV Could Drive Treatment

Findings could support new vaccine development to mitigate rapid virus mutation. Medscape Medical News

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Medical Xpress broke the news in on Wednesday, July 30, 2025.
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