
95% of researchers rate our articles as excellent or good
Learn more about the work of our research integrity team to safeguard the quality of each article we publish.
Find out more
BRIEF RESEARCH REPORT article
Front. Med.
Sec. Infectious Diseases: Pathogenesis and Therapy
Volume 12 - 2025 | doi: 10.3389/fmed.2025.1562537
The final, formatted version of the article will be published soon.
You have multiple emails registered with Frontiers:
Please enter your email address:
If you already have an account, please login
You don't have a Frontiers account ? You can register here
The CD4/CD8 ratio has emerged as a useful indicator of immune dysfunction and comorbid conditions in people living with HIV (PLWH).However, its optimal cut-off value is unclear.We explored the correlation between the CD4/CD8 ratio, immunosenescence markers and comorbid conditions.We prospectively included PLWH on successful and stable ART (antiretroviral therapy) > 60 years old and receiving either BIC/FTC/TAF or DTG/3TC, in Nice, France. HIV-negative healthy subjects were included as controls. We measured T-cell subsets (naïve, central memory, effector memory and terminally differentiated cells) and the distribution of KLRG1+CD57+ senescent cells. We correlated CD4/CD8 ratio, background measurements and comorbid conditions.We included 68 PLWH (median age 69 years, 31 years on ART, median CD4/CD8 ratio 0.76).PLWH had higher levels of senescence markers than controls (n=8). Among PLWH, adjusting for age, gender, HIV follow-up and duration on ART, those with a CD4/CD8 ratio < 0.76 had more senescent CD8+ cells (AdjOR=0.93, 95%CI=[0.88 ; 0.97], p-value=0.003). Higher levels of CD8+ senescence persisted for lower CD4/CD8 ratios, with, in addition, a significant decrease in NK cells in case of a ratio < 0.4.After adjustment, CD8+ effector memory senescent cells were significantly more abundant in PLWH with hypertension.Conclusions: PLWH on successful ART display elevated immunosenescence markers, mainly on CD8+ T-cells. A CD4/CD8 cut-off value below 0.4 showed the strongest association with immune dysfunction, including NK+ cells. Such results could be useful for identifying patients requiring closer follow-up and screening for complications.
Keywords: HIV, CD4/CD8 ratio, immunosenescence, Comorbidity, immune activation
Received: 17 Jan 2025; Accepted: 28 Mar 2025.
Copyright: © 2025 Vassallo, Jacques, Ticchioni, Fabre, Chirio, Naqvi, Cua, Ameil, Godemert, Pradier and Carles. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Matteo Vassallo, Centre Hospitalier de Cannes, Cannes, France
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Research integrity at Frontiers
Learn more about the work of our research integrity team to safeguard the quality of each article we publish.