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Review
. 2024 Nov 1;19(6):293-304.
doi: 10.1097/COH.0000000000000881. Epub 2024 Aug 21.

Preventing perinatal HIV acquisition; current gaps and future perspectives

Affiliations
Review

Preventing perinatal HIV acquisition; current gaps and future perspectives

Beatrice Cockbain et al. Curr Opin HIV AIDS. .

Abstract

Purpose of review: Although current treatment could eradicate vertical transmission, in 2022, 130 000 infants acquired HIV globally. HIV suppression with antiretroviral therapy (ART) transforms survival for people living with HIV (PLWH), and prevents transmission, including vertical. International guidelines recommend lifelong ART for PLWH, consequently perinatal HIV acquisition reflects implementation gaps in the HIV care cascade. We summarize these gaps, exploring potential novel approaches and therapeutic innovations towards eliminating vertical HIV transmission.

Recent findings: Multifactorial challenges continue to underpin gaps in the HIV care cascade, including accessibility, availability and sustainability of HIV testing, prevention and treatment, alongside stigma, gender-based violence and poverty. Long-acting ART may be important in preventing perinatal HIV acquisition, with early data demonstrating tolerability and efficacy of injectable ART throughout pregnancy, both as HIV treatment and prevention. Carefully selected long-acting broadly neutralizing antibodies (bNAbs) matching circulating, exposing viral envelope sequences have demonstrated safety, clinical trials are ongoing to demonstrate efficacy.

Summary: Emerging clinical studies should prioritize pregnant/lactating people and infants to ensure such therapies are well tolerated and efficacious. Alongside therapeutic innovation, programmatic strategies must address social and economic challenges, ensuring sustainable HIV treatment/prevention programmes and facilitating global elimination of blood-borne viruses.

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Conflict of interest statement

B.C. is in receipt of a National Institute of Health Research (NIHR) Academic Clinical Fellowship. S.F. is supported by the Imperial College NIHR Biomedical Research Centre and has received grant money to her institution from Viiv, Gilead, and AbbVie.

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