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TREX1 531C/T Polymorphism and Autoantibodies Associated with the Immune Status of HIV-1-Infected Individuals
Autoimmune diseases can develop during HIV-1 infection, mainly related to the individual’s immune competence. The study investigated the association of the TREX1 531C/T polymorphism and antinuclear antibodies (ANA) in HIV-1 infection and the time of antiretroviral therapy (ART) used. Cross-sectional...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253649/ https://www.ncbi.nlm.nih.gov/pubmed/37298611 http://dx.doi.org/10.3390/ijms24119660 |
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author | Queiroz, Maria Alice Freitas Moura, Tuane Carolina Ferreira Bichara, Carlos David Araújo de Lima, Lorena Leticia Peixoto de Oliveira, Allysson Quintino Tenório de Souza, Ranilda Gama Gomes, Samara Tatielle Monteiro Amoras, Ednelza da Silva Graça Vallinoto, Antonio Carlos Rosário |
author_facet | Queiroz, Maria Alice Freitas Moura, Tuane Carolina Ferreira Bichara, Carlos David Araújo de Lima, Lorena Leticia Peixoto de Oliveira, Allysson Quintino Tenório de Souza, Ranilda Gama Gomes, Samara Tatielle Monteiro Amoras, Ednelza da Silva Graça Vallinoto, Antonio Carlos Rosário |
author_sort | Queiroz, Maria Alice Freitas |
collection | PubMed |
description | Autoimmune diseases can develop during HIV-1 infection, mainly related to the individual’s immune competence. The study investigated the association of the TREX1 531C/T polymorphism and antinuclear antibodies (ANA) in HIV-1 infection and the time of antiretroviral therapy (ART) used. Cross-sectional and longitudinal assessments were carried out in 150 individuals, divided into three groups: ART-naïve, 5 years and 10 years on ART; ART-naïve individuals were evaluated for 2 years after initiation of treatment. The individuals’ blood samples were submitted to indirect immunofluorescence tests, real-time PCR and flow cytometry. The TREX1 531C/T polymorphism was associated with higher levels of TCD4(+) lymphocytes and IFN-α in individuals with HIV-1. Individuals on ART had a higher frequency of ANA, higher levels of T CD4(+) lymphocytes, a higher ratio of T CD4(+)/CD8(+) lymphocytes and higher levels of IFN-α than therapy-naïve individuals (p < 0.05). The TREX1 531C/T polymorphism was associated with better maintenance of the immune status of individuals with HIV-1 and ANA with immune restoration in individuals on ART, indicating the need to identify individuals at risk of developing an autoimmune disease. |
format | Online Article Text |
id | pubmed-10253649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102536492023-06-10 TREX1 531C/T Polymorphism and Autoantibodies Associated with the Immune Status of HIV-1-Infected Individuals Queiroz, Maria Alice Freitas Moura, Tuane Carolina Ferreira Bichara, Carlos David Araújo de Lima, Lorena Leticia Peixoto de Oliveira, Allysson Quintino Tenório de Souza, Ranilda Gama Gomes, Samara Tatielle Monteiro Amoras, Ednelza da Silva Graça Vallinoto, Antonio Carlos Rosário Int J Mol Sci Article Autoimmune diseases can develop during HIV-1 infection, mainly related to the individual’s immune competence. The study investigated the association of the TREX1 531C/T polymorphism and antinuclear antibodies (ANA) in HIV-1 infection and the time of antiretroviral therapy (ART) used. Cross-sectional and longitudinal assessments were carried out in 150 individuals, divided into three groups: ART-naïve, 5 years and 10 years on ART; ART-naïve individuals were evaluated for 2 years after initiation of treatment. The individuals’ blood samples were submitted to indirect immunofluorescence tests, real-time PCR and flow cytometry. The TREX1 531C/T polymorphism was associated with higher levels of TCD4(+) lymphocytes and IFN-α in individuals with HIV-1. Individuals on ART had a higher frequency of ANA, higher levels of T CD4(+) lymphocytes, a higher ratio of T CD4(+)/CD8(+) lymphocytes and higher levels of IFN-α than therapy-naïve individuals (p < 0.05). The TREX1 531C/T polymorphism was associated with better maintenance of the immune status of individuals with HIV-1 and ANA with immune restoration in individuals on ART, indicating the need to identify individuals at risk of developing an autoimmune disease. MDPI 2023-06-02 /pmc/articles/PMC10253649/ /pubmed/37298611 http://dx.doi.org/10.3390/ijms24119660 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Queiroz, Maria Alice Freitas Moura, Tuane Carolina Ferreira Bichara, Carlos David Araújo de Lima, Lorena Leticia Peixoto de Oliveira, Allysson Quintino Tenório de Souza, Ranilda Gama Gomes, Samara Tatielle Monteiro Amoras, Ednelza da Silva Graça Vallinoto, Antonio Carlos Rosário TREX1 531C/T Polymorphism and Autoantibodies Associated with the Immune Status of HIV-1-Infected Individuals |
title | TREX1 531C/T Polymorphism and Autoantibodies Associated with the Immune Status of HIV-1-Infected Individuals |
title_full | TREX1 531C/T Polymorphism and Autoantibodies Associated with the Immune Status of HIV-1-Infected Individuals |
title_fullStr | TREX1 531C/T Polymorphism and Autoantibodies Associated with the Immune Status of HIV-1-Infected Individuals |
title_full_unstemmed | TREX1 531C/T Polymorphism and Autoantibodies Associated with the Immune Status of HIV-1-Infected Individuals |
title_short | TREX1 531C/T Polymorphism and Autoantibodies Associated with the Immune Status of HIV-1-Infected Individuals |
title_sort | trex1 531c/t polymorphism and autoantibodies associated with the immune status of hiv-1-infected individuals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253649/ https://www.ncbi.nlm.nih.gov/pubmed/37298611 http://dx.doi.org/10.3390/ijms24119660 |
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