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Impact of first-line antiretroviral therapy regimens on the restoration of the CD4/CD8 ratio in the CNICS cohort.
Herrera, Sabina; Fernandez-Felix, Borja M; Hunt, Peter W; Deeks, Steven G; Sainz, Talía; Heath, Sonya L; Achenbach, Chad J; Rodríguez, Benigno; Mathews, Christopher; Christopoulos, Katerina; Mayer, Kenneth; Napravnik, Sonia; Moreno, Santiago; Serrano-Villar, Sergio.
Afiliación
  • Herrera S; University Hospital Ramón y Cajal and Universidad de Alcalá (IRYCIS), Madrid, 28034, Spain.
  • Fernandez-Felix BM; University Hospital Ramón y Cajal and Universidad de Alcalá (IRYCIS), Madrid, 28034, Spain.
  • Hunt PW; University of California, San Francisco, CA 91143, USA.
  • Deeks SG; University of California, San Francisco, CA 91143, USA.
  • Sainz T; University Hospital La Paz and Universidad Autónoma (IdIPAZ), Madrid, 28046, Spain.
  • Heath SL; University of Alabama, Birmingham, AL 35294, USA.
  • Achenbach CJ; Northwestern University, Evanston, IL 60201, USA.
  • Rodríguez B; Case Western Reserve University, Cleveland, OH 44106, USA.
  • Mathews C; University of California, San Diego, CA 92110, USA.
  • Christopoulos K; University of California, San Francisco, CA 91143, USA.
  • Mayer K; Fenway Health and Harvard School of Public Health, Boston, MA 02116, USA.
  • Napravnik S; University of North Carolina, Chapel Hill, NC 27599, USA.
  • Moreno S; University Hospital Ramón y Cajal and Universidad de Alcalá (IRYCIS), Madrid, 28034, Spain.
  • Serrano-Villar S; University Hospital Ramón y Cajal and Universidad de Alcalá (IRYCIS), Madrid, 28034, Spain.
J Antimicrob Chemother ; 75(6): 1604-1610, 2020 06 01.
Article en En | MEDLINE | ID: mdl-32211777
ABSTRACT

BACKGROUND:

The CD4/CD8 ratio is an indicator of immunosenescence and a predictor of all-cause mortality in HIV-infected patients. The effects of different ART regimens on CD4/CD8 ratio recovery remain unclear.

METHODS:

Clinical cohort study of ART-treated patients from the CFAR Network of Integrated Clinical Systems (CNICS). We included ART-naive adults with HIV infection who achieved undetectable HIV RNA during the first 48 weeks of treatment and had additional follow-up 48 weeks after virological suppression (VS). Primary endpoints included increase in CD4/CD8 ratio at both timepoints and secondary endpoints were CD4/CD8 ratio recovery at cut-offs of ≥0.5 or ≥1.0.

RESULTS:

Of 3971 subjects who met the study criteria, 1876 started ART with an NNRTI, 1804 with a PI and 291 with an integrase strand transfer inhibitor (INSTI). After adjusting for age, sex, race, year of entry, risk group, HCV serostatus, baseline viral load and baseline CD4/CD8 ratio, subjects on an NNRTI showed a significantly greater CD4/CD8 ratio gain compared with those on a PI, either 48 weeks after ART initiation or after 48 weeks of HIV RNA VS. The greater CD4/CD8 ratio improvement in the NNRTI arm was driven by a higher decline in CD8 counts. The INSTI group showed increased rates of CD4/CD8 ratio normalization at the ≥1.0 cut-off compared with the PI group.

CONCLUSIONS:

NNRTI therapy was associated with a greater increase in the CD4/CD8 ratio compared with PIs. NNRTI- and INSTI-based first-line ART were associated with higher rates of CD4/CD8 ratio normalization at a cut-off of 1.0 than a PI-based regimen, which might have clinical implications.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / Fármacos Anti-VIH Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: J Antimicrob Chemother Año: 2020 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / Fármacos Anti-VIH Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: J Antimicrob Chemother Año: 2020 Tipo del documento: Article País de afiliación: España