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Discordant Immune Response Among Treatment Experienced Patients Infected With Hiv-1: Crosstalk Between Mirnas Expression and Cd4+ T Cells Count Publisher Pubmed



Poorghobadi S1 ; Agharezaei M1 ; Ghanbari M2 ; Bahramali G1 ; Abbasian L3 ; Sajadipour M4 ; Baesi K1
Authors
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Authors Affiliations
  1. 1. Hepatitis and AIDS Department, Pasteur Institute of Iran, Tehran, Iran
  2. 2. Department of Microbial Biotechnology, Faculty of Biological Science, Tehran North Branch, Islamic Azad University, Tehran, Iran
  3. 3. Department of Infectious Diseases and Tropical Medicine, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. South Health Center, Tehran University of Medical Sciences, Tehran, Iran

Source: International Immunopharmacology Published:2023


Abstract

Background: One of the problems with treating HIV-infected patients with ARVs is that the treatment can reduce viral load and does not increase the number of CD4 cells (immunological discordance). There are still challenges to treating HIV-positive patients. Aim: This study aimed to investigate the expression level of 18 miRNAs involved in the proliferation and differentiation of CD4+ T cells in a target (discordant immune response) and a control (immune response) group. Methods: In this case-control study, 18 miRNAs were selected and synthesized according to the in-silico analysis and published literatures. RNA extraction was performed from PBMC cells of 30 HIV-1 positive patients in the sample bank. The expression level of microRNAs was calculated by the relative q PCR method (2−ΔΔCt method), and data were analyzed using GraphPad Prism software version 8.0.2. Results: The results of fold change calculation and statistical analysis showed that the expression levels of miR-30b (p value: 0.01, fold change: 0.23), miR-155 (p value: 0.04, fold change: 0.44), miR-181a (p value: 0.01, fold change: 0.37), and miR-190b (p value: 0.01, fold change: 0.39) had a significant decrease in the target group compared to the control group. Conclusion: In summary, various studies have shown that miRNAs, including miR-30b, miR-155, miR-181a, and miR-190b, are involved in the proliferation, differentiation, and development of CD4+ T cells. One reason for the lack of increase in CD4+ T cells may be the reduced expression of these miRNAs. © 2022 Elsevier B.V.
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