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IL-31 expression in HIV-infected patients with different routes of disease transmission
Acquired immunodeficiency syndrome (AIDS) is caused by the human immunodeficiency virus (HIV). AIDS is characterized by an impaired immune system and low cellular immunity. The main manifestation of AIDS is a reduction in the number of CD4(+) T cells and alteration in cytokine concentration. The pre...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276414/ https://www.ncbi.nlm.nih.gov/pubmed/35758393 http://dx.doi.org/10.1097/MD.0000000000029509 |
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author | Yan, Changxin Xu, Huafeng Rong, Chunli Cao, Meilin Miao, Zhuo Zhou, Haizhou |
author_facet | Yan, Changxin Xu, Huafeng Rong, Chunli Cao, Meilin Miao, Zhuo Zhou, Haizhou |
author_sort | Yan, Changxin |
collection | PubMed |
description | Acquired immunodeficiency syndrome (AIDS) is caused by the human immunodeficiency virus (HIV). AIDS is characterized by an impaired immune system and low cellular immunity. The main manifestation of AIDS is a reduction in the number of CD4(+) T cells and alteration in cytokine concentration. The present work aimed to explore the expression of IL-31 in HIV infection and disease progression. Serum samples were collected from HIV-infected patients with different routes of disease transmission. The subjects included 24 patients who were infected with HIV upon blood transmission and 36 patients who had acquired the disease through sexual transmission (21 cases of homosexual transmission and 15 cases of heterosexual transmission). In addition, 20 normal healthy individuals were included to serve as the control group. The levels of IL-31 in the collected serum samples were estimated using the human IL-31 Platinum ELISA kit. The serum analysis results revealed that the concentration of IL-31 in the serum samples for the blood transmission, sexually transmission, and normal group patients was 4.07 ± 1.63 pg/L, 7.43 ± 1.15 pg/L, and 2.87 ± 1.04 pg/L, respectively. The statistical analysis revealed that the concentration of IL-31 in HIV-1 infection was higher than that in the normal control. In addition, the expression of IL-31 was significantly higher in the sexual transmission group compared to the blood transmission group (P < .05). IL-31 could have an important role in HIV infection, although the role of IL-31 in disease progression in HIV-infected individuals requires further research. |
format | Online Article Text |
id | pubmed-9276414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-92764142022-08-01 IL-31 expression in HIV-infected patients with different routes of disease transmission Yan, Changxin Xu, Huafeng Rong, Chunli Cao, Meilin Miao, Zhuo Zhou, Haizhou Medicine (Baltimore) 4850 Acquired immunodeficiency syndrome (AIDS) is caused by the human immunodeficiency virus (HIV). AIDS is characterized by an impaired immune system and low cellular immunity. The main manifestation of AIDS is a reduction in the number of CD4(+) T cells and alteration in cytokine concentration. The present work aimed to explore the expression of IL-31 in HIV infection and disease progression. Serum samples were collected from HIV-infected patients with different routes of disease transmission. The subjects included 24 patients who were infected with HIV upon blood transmission and 36 patients who had acquired the disease through sexual transmission (21 cases of homosexual transmission and 15 cases of heterosexual transmission). In addition, 20 normal healthy individuals were included to serve as the control group. The levels of IL-31 in the collected serum samples were estimated using the human IL-31 Platinum ELISA kit. The serum analysis results revealed that the concentration of IL-31 in the serum samples for the blood transmission, sexually transmission, and normal group patients was 4.07 ± 1.63 pg/L, 7.43 ± 1.15 pg/L, and 2.87 ± 1.04 pg/L, respectively. The statistical analysis revealed that the concentration of IL-31 in HIV-1 infection was higher than that in the normal control. In addition, the expression of IL-31 was significantly higher in the sexual transmission group compared to the blood transmission group (P < .05). IL-31 could have an important role in HIV infection, although the role of IL-31 in disease progression in HIV-infected individuals requires further research. Lippincott Williams & Wilkins 2022-06-24 /pmc/articles/PMC9276414/ /pubmed/35758393 http://dx.doi.org/10.1097/MD.0000000000029509 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) |
spellingShingle | 4850 Yan, Changxin Xu, Huafeng Rong, Chunli Cao, Meilin Miao, Zhuo Zhou, Haizhou IL-31 expression in HIV-infected patients with different routes of disease transmission |
title | IL-31 expression in HIV-infected patients with different routes of disease transmission |
title_full | IL-31 expression in HIV-infected patients with different routes of disease transmission |
title_fullStr | IL-31 expression in HIV-infected patients with different routes of disease transmission |
title_full_unstemmed | IL-31 expression in HIV-infected patients with different routes of disease transmission |
title_short | IL-31 expression in HIV-infected patients with different routes of disease transmission |
title_sort | il-31 expression in hiv-infected patients with different routes of disease transmission |
topic | 4850 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276414/ https://www.ncbi.nlm.nih.gov/pubmed/35758393 http://dx.doi.org/10.1097/MD.0000000000029509 |
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