Nadir CD4 Is Negatively Associated With Antinuclear Antibody Detection in HCV/HIV-Coinfected Patients

J Acquir Immune Defic Syndr. 2019 Apr 1;80(4):461-466. doi: 10.1097/QAI.0000000000001940.

Abstract

Background: Hepatitis C virus (HCV) and HIV infections are associated with higher risk of autoimmune diseases and T-cell dysfunction.

Setting: We evaluate prevalence and factors associated with the presence of autoimmune antinuclear (ANA), anti-smooth muscle actin (aSMA), and anti-liver kidney microsome (aLKM1) antibodies (Ab) in HCV/HIV-coinfected patients during the post-combined antiretroviral therapy era.

Methods: A cross-sectional observational study nested in the ANRS CO13 HEPAVIH cohort (NCT number: NCT03324633). We selected patients with both ANA testing and T-cell immunophenotyping determination during the cohort follow-up and collected aLKM1 and aSMA data when available. Logistic regression models were built to determine factors associated with the presence of auto-Ab.

Results: Two hundred twenty-three HCV/HIV-coinfected patients fulfilled selection criteria. Prevalence of ANA and aSMA was 43.5% and 23.2%, respectively, and both were detected in 13.3% of patients. Isolated aSMA were detected in 9.9% and aLKM1 in 2 patients. In multivariable analysis, only a low nadir CD4 T-cell count was significantly associated with ANA detection.

Conclusions: ANA and aSMA detection remain frequent in HCV/HIV-coinfected patients during the post-combined antiretroviral therapy era, despite fair immune restoration. These results advocate for a close monitoring of ANA before immune checkpoint inhibitor therapy in these patients with greater caution for those with a low nadir CD4 T-cell count.

Publication types

  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / immunology*
  • Antibodies, Antinuclear / blood*
  • Autoimmune Diseases / complications
  • Autoimmune Diseases / epidemiology*
  • CD4 Lymphocyte Count
  • Coinfection / immunology
  • Coinfection / virology
  • Cross-Sectional Studies
  • Female
  • HIV Infections / complications
  • HIV Infections / immunology*
  • HIV-1 / immunology
  • Hepacivirus / immunology
  • Hepatitis C / complications
  • Hepatitis C / immunology*
  • Humans
  • Male
  • Microsomes, Liver / immunology*
  • Middle Aged
  • T-Lymphocytes / immunology

Substances

  • ACTA2 protein, human
  • Actins
  • Antibodies, Antinuclear

Associated data

  • ClinicalTrials.gov/NCT03324633