Impact of very early antiretroviral therapy during acute HIV infection on long-term immunovirological outcomes

• Published in: International journal of infectious diseases Vol. 136; pp. 100 - 106
• Main Authors: Suanzes, Paula, Navarro, Jordi, Rando-Segura, Ariadna, Álvarez-López, Patricia, García, Jorge, Descalzo, Vicente, Monforte, Arnau, Arando, Maider, Rodríguez, Lucía, Planas, Bibiana, Burgos, Joaquín, Curran, Adrian, Buzón, María José, Falcó, Vicenç
• Format: Journal Article
• Language: English
• Published: Elsevier Ltd 01.11.2023; Elsevier
• Subjects: Acute HIV infection; Antiretroviral treatment; CD4+/CD8+ ratio; Early treatment; HIV infection; Immune recovery; Acute HIV infection; CD4+/CD8+ ratio; Early treatment; HIV infection; Immune recovery; Antiretroviral treatment
• ISSN: 1201-9712; 1878-3511
• DOI: 10.1016/j.ijid.2023.09.009

•The CD4+/CD8+ ratio pre-treatment is the strongest predictor of immune recovery.•The immune benefits of early antiretroviral therapy might derive from higher pre- antiretroviral therapy CD4+/CD8+ ratios.•Treatment with integrase inhibitors might be related to earlier immune recovery. We aimed to determine if starting antiretroviral therapy (ART) in the first 30 days after acquiring HIV infection has an impact on immunovirological response. Observational, ambispective study including 147 patients with confirmed acute HIV infection (January/1995-August/2022). ART was defined as very early (≤30 days after the estimated date of infection), early (31-180 days), and late (>180 days). We compared time to viral suppression (viral load [VL] <50 copies/ml) and immune recovery (IR) (CD4+/CD8+ ratio ≥1) according to the timing and type of ART using survival analysis. ART was started in 140 (95.2%) patients. ART was very early in 24 (17.1%), early in 77 (55.0%), and late in 39 (27.9%) cases. Integrase strand transfer inhibitor (INSTI)-based regimens were the most used in both the overall population (65%) and the very early ART group (23/24, 95.8%). Median HIV VL and CD4+/CD8+ ratio pre-ART were higher in the very early ART group (P <0.05). Patients in the very early and early ART groups and treated with INSTI-based regimens achieved IR earlier (P <0.05). Factors associated with faster IR were the CD4+/CD8+ ratio pre-ART (hazard ratio: 9.3, 95% CI: 3.1-27.8, P <0.001) and INSTI-based regimens (hazard ratio: 2.4, 95% CI: 1.3-4.2, P = 0.003). The strongest predictors of IR in patients who start ART during AHI are the CD4+/CD8+ ratio pre-ART and INSTI-based ART regimens.