Dec 3, 2024, 1:04 PM
Dec 3, 2024, 1:04 PM

HepB-CpG vaccine offers stronger protection for people living with HIV

Highlights
  • The ACTG announced the publication of the BEe-HIVe trial results in JAMA, focusing on the HepB-CpG vaccine's efficacy among HIV patients.
  • The trial found that the HepB-CpG vaccine delivered significantly higher protection against hepatitis B compared to traditional vaccines.
  • These results provide strong evidence for the re-vaccination of people living with HIV who did not benefit from standard hepatitis B vaccines.
Story

In a significant development on December 3, 2024, researchers from the ACTG announced findings from the BEe-HIVe randomized clinical trial, published in JAMA. This international study focused on evaluating the effectiveness of the HepB-CpG vaccine in protecting individuals living with HIV, particularly those who had previously not responded to conventional hepatitis B vaccines. The trial provided essential data regarding the vulnerability of these individuals to hepatitis B and highlighted the inadequacies of traditional vaccination methods. Approximately 55 million people are living with HIV around the world, often facing challenges in developing protective immune responses following vaccination. Hepatitis B is a serious health risk for this population, frequently leading to liver complications, including cirrhosis and liver cancer. The BEe-HIVe trial involved participants who were on antiretroviral therapy and had a history of poor responses to conventional hepatitis B vaccinations. The study setup included randomizing participants into three groups, with two groups receiving different doses of the HepB-CpG vaccine, while the control group received the conventional hepatitis B vaccine. The results were promising, showing a remarkable 99% protection rate for those who received three doses of the HepB-CpG vaccine and 93% for those receiving two doses, compared to only 81% for participants who were administered the conventional vaccine. As hepatitis B poses significant long-term health risks, assessors emphasized how important it is to reassess vaccination strategies within vulnerable populations, particularly those living with HIV. The implications of these findings are profound: if adopted widely, this new vaccination could prevent a great deal of morbidity and mortality related to hepatitis B within this demographic. The safety profile of the HepB-CpG vaccine appeared reassuring, with no unexpected safety concerns reported during the trial. The study adds to a compelling body of evidence advocating for re-vaccination of individuals who did not initially respond to traditional hepatitis B vaccines. Through this, healthcare providers could significantly mitigate the risk of hepatitis B infection among those more susceptible due to their HIV status. Long-term follow-up will continue, with more data expected in 2025, aiming for a comprehensive understanding of the lasting efficacy and safety regarding the HepB-CpG vaccination in this vulnerable group.

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