AI Article Synopsis

  • Mesalamine, an anti-inflammatory drug, was tested for its effects on mucosal inflammation in HIV-infected individuals with low CD4 counts and under antiretroviral therapy.
  • A clinical trial randomized 33 subjects to receive either mesalamine or placebo for 12 weeks, followed by a crossover to the other treatment for another 12 weeks.
  • The results showed no significant changes in immune activation markers or CD4+ T cell counts in those treated with mesalamine compared to the placebo group, indicating mesalamine did not affect the ongoing immune activation linked to HIV infection.

Article Abstract

Unlabelled: The anti-inflammatory agent, mesalamine (5-aminosalicylic acid) has been shown to decrease mucosal inflammation in ulcerative colitis. The effect of mesalamine in HIV-infected individuals, who exhibit abnormal mucosal immune activation and microbial translocation (MT), has not been established in a placebo-controlled trial. We randomized 33 HIV-infected subjects with CD4 counts <350 cells/mm3 and plasma HIV RNA levels <40 copies/ml on antiretroviral therapy (ART) to add mesalamine vs. placebo to their existing regimen for 12 weeks followed by a 12 week crossover to the other arm. Compared to placebo-treated subjects, mesalamine-treated subjects did not experience any significant change in the percent CD38+HLA-DR+ peripheral blood CD4+ and CD8+ T cells at week 12 (P = 0.38 and P = 0.63, respectively), or in the CD4+ T cell count at week 12 (P = 0.83). The percent CD38+HLA-DR+ CD4+ and CD8+ T cells also did not change significantly in rectal tissue (P = 0.86, P = 0.84, respectively). During the period of mesalamine administration, plasma sCD14, IL-6, D-dimer, and kynurenine to tryptophan ratio were not changed significantly at week 12 and were similarly unchanged at week 24. This study suggests that, at least under the conditions studied, the persistent immune activation associated with HIV infection is not impacted by the anti-inflammatory effects of mesalamine.

Trial Registration: ClinicalTrials.gov NCT01090102.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283685PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0116306PLOS

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