Impact of Previous HPV Infection and CD4 T-Cell Levels on Immune Responses to a Three-Dose Nonavalent HPV Vaccine in Individuals with HIV Undergoing ART - Summary - MDSpire

Impact of Previous HPV Infection and CD4 T-Cell Levels on Immune Responses to a Three-Dose Nonavalent HPV Vaccine in Individuals with HIV Undergoing ART

  • By

  • Eeva Tortellini

  • Mariasilvia Guardiani

  • Anna Carraro

  • Lorenzo Ansaldo

  • Sara Corazza

  • Sara Giovanna De Maria

  • Silvia Garattini

  • Mirko Barresi

  • Valeria Belvisi

  • Maria Antonella Zingaropoli

  • Federica Dominelli

  • Carmen Falvino

  • Fabio Mengoni

  • Alessandro Tavelli

  • Cristina Giambi

  • Claudio Maria Mastroianni

  • Cosmo Del Borgo

  • Raffaella Marocco

  • Miriam Lichtner

  • December 24, 2025

  • 0 min

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Objective:

To characterize the T-cell response to the Gardasil 9® HPV vaccine in people with HIV (PWH), focusing on the effects of prior HPV infection and CD4 T-cell count, and to assess the implications for vaccination strategies.

Key Findings:
  • PWH have a higher incidence of HPV infection and related cancers compared to HIV-uninfected individuals, necessitating targeted vaccination efforts.
  • The immune response to the Gardasil 9® vaccine in PWH is comparable to that in the general population, indicating effective immunogenicity.
  • Higher CD4 T-cell counts correlate with better T-cell responses to the vaccine, suggesting the need for monitoring CD4 levels in vaccination strategies.
  • Prior HPV infection status influences T-cell responses post-vaccination, highlighting the importance of individual patient history.
Interpretation:

The study suggests that both prior HPV infection and CD4 T-cell levels significantly affect the immune response to the HPV vaccine in PWH, emphasizing the need for tailored vaccination strategies to enhance efficacy.

Limitations:
  • The study was conducted at a single center, which may limit generalizability and applicability to broader populations.
  • Exclusion of individuals with other chronic viral infections may affect the findings, potentially underrepresenting the complexity of immune responses in diverse patient populations.
Conclusion:

The findings underscore the importance of considering prior HPV infection and CD4 T-cell counts when evaluating vaccine responses in PWH, suggesting potential avenues for improving vaccination strategies tailored to individual patient profiles.

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