HIV infection and cardiovascular disease have both shared and distinct monocyte gene expression features: Women's Interagency HIV study.

Persistent inflammation contributes to the development of cardiovascular disease (CVD) as an HIV-associated comorbidity. Innate immune cells such as monocytes are major drivers of inflammation in men and women with HIV. The study objectives are to examine the contribution of circulating non-classica...

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Main Authors: Juan Lin, Erik Ehinger, David B Hanna, Qibin Qi, Tao Wang, Yanal Ghosheh, Karin Mueller, Kathryn Anastos, Jason M Lazar, Wendy J Mack, Phyllis C Tien, Joan W Berman, Mardge H Cohen, Igho Ofotokun, Stephen Gange, Chenglong Liu, Sonya L Heath, Russell P Tracy, Howard N Hodis, Alan L Landay, Klaus Ley, Robert C Kaplan
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0285926
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author Juan Lin
Erik Ehinger
David B Hanna
Qibin Qi
Tao Wang
Yanal Ghosheh
Karin Mueller
Kathryn Anastos
Jason M Lazar
Wendy J Mack
Phyllis C Tien
Joan W Berman
Mardge H Cohen
Igho Ofotokun
Stephen Gange
Chenglong Liu
Sonya L Heath
Russell P Tracy
Howard N Hodis
Alan L Landay
Klaus Ley
Robert C Kaplan
author_facet Juan Lin
Erik Ehinger
David B Hanna
Qibin Qi
Tao Wang
Yanal Ghosheh
Karin Mueller
Kathryn Anastos
Jason M Lazar
Wendy J Mack
Phyllis C Tien
Joan W Berman
Mardge H Cohen
Igho Ofotokun
Stephen Gange
Chenglong Liu
Sonya L Heath
Russell P Tracy
Howard N Hodis
Alan L Landay
Klaus Ley
Robert C Kaplan
author_sort Juan Lin
collection DOAJ
description Persistent inflammation contributes to the development of cardiovascular disease (CVD) as an HIV-associated comorbidity. Innate immune cells such as monocytes are major drivers of inflammation in men and women with HIV. The study objectives are to examine the contribution of circulating non-classical monocytes (NCM, CD14dimCD16+) and intermediate monocytes (IM, CD14+CD16+) to the host response to long-term HIV infection and HIV-associated CVD. Women with and without chronic HIV infection (H) were studied. Subclinical CVD (C) was detected as plaques imaged by B-mode carotid artery ultrasound. The study included H-C-, H+C-, H-C+, and H+C+ participants (23 of each, matched on race/ethnicity, age and smoking status), selected from among enrollees in the Women's Interagency HIV Study. We assessed transcriptomic features associated with HIV or CVD alone or comorbid HIV/CVD comparing to healthy (H-C-) participants in IM and NCM isolated from peripheral blood mononuclear cells. IM gene expression was little affected by HIV alone or CVD alone. In IM, coexisting HIV and CVD produced a measurable gene transcription signature, which was abolished by lipid-lowering treatment. In NCM, versus non-HIV controls, women with HIV had altered gene expression, irrespective of whether or not they had comorbid CVD. The largest set of differentially expressed genes was found in NCM among women with both HIV and CVD. Genes upregulated in association with HIV included several potential targets of drug therapies, including LAG3 (CD223). In conclusion, circulating monocytes from patients with well controlled HIV infection demonstrate an extensive gene expression signature which may be consistent with the ability of these cells to serve as potential viral reservoirs. Gene transcriptional changes in HIV patients were further magnified in the presence of subclinical CVD.
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spelling doaj.art-f3b755da3995493bb9bc5b3e08f13d9a2024-02-01T05:32:13ZengPublic Library of Science (PLoS)PLoS ONE1932-62032023-01-01185e028592610.1371/journal.pone.0285926HIV infection and cardiovascular disease have both shared and distinct monocyte gene expression features: Women's Interagency HIV study.Juan LinErik EhingerDavid B HannaQibin QiTao WangYanal GhoshehKarin MuellerKathryn AnastosJason M LazarWendy J MackPhyllis C TienJoan W BermanMardge H CohenIgho OfotokunStephen GangeChenglong LiuSonya L HeathRussell P TracyHoward N HodisAlan L LandayKlaus LeyRobert C KaplanPersistent inflammation contributes to the development of cardiovascular disease (CVD) as an HIV-associated comorbidity. Innate immune cells such as monocytes are major drivers of inflammation in men and women with HIV. The study objectives are to examine the contribution of circulating non-classical monocytes (NCM, CD14dimCD16+) and intermediate monocytes (IM, CD14+CD16+) to the host response to long-term HIV infection and HIV-associated CVD. Women with and without chronic HIV infection (H) were studied. Subclinical CVD (C) was detected as plaques imaged by B-mode carotid artery ultrasound. The study included H-C-, H+C-, H-C+, and H+C+ participants (23 of each, matched on race/ethnicity, age and smoking status), selected from among enrollees in the Women's Interagency HIV Study. We assessed transcriptomic features associated with HIV or CVD alone or comorbid HIV/CVD comparing to healthy (H-C-) participants in IM and NCM isolated from peripheral blood mononuclear cells. IM gene expression was little affected by HIV alone or CVD alone. In IM, coexisting HIV and CVD produced a measurable gene transcription signature, which was abolished by lipid-lowering treatment. In NCM, versus non-HIV controls, women with HIV had altered gene expression, irrespective of whether or not they had comorbid CVD. The largest set of differentially expressed genes was found in NCM among women with both HIV and CVD. Genes upregulated in association with HIV included several potential targets of drug therapies, including LAG3 (CD223). In conclusion, circulating monocytes from patients with well controlled HIV infection demonstrate an extensive gene expression signature which may be consistent with the ability of these cells to serve as potential viral reservoirs. Gene transcriptional changes in HIV patients were further magnified in the presence of subclinical CVD.https://doi.org/10.1371/journal.pone.0285926
spellingShingle Juan Lin
Erik Ehinger
David B Hanna
Qibin Qi
Tao Wang
Yanal Ghosheh
Karin Mueller
Kathryn Anastos
Jason M Lazar
Wendy J Mack
Phyllis C Tien
Joan W Berman
Mardge H Cohen
Igho Ofotokun
Stephen Gange
Chenglong Liu
Sonya L Heath
Russell P Tracy
Howard N Hodis
Alan L Landay
Klaus Ley
Robert C Kaplan
HIV infection and cardiovascular disease have both shared and distinct monocyte gene expression features: Women's Interagency HIV study.
PLoS ONE
title HIV infection and cardiovascular disease have both shared and distinct monocyte gene expression features: Women's Interagency HIV study.
title_full HIV infection and cardiovascular disease have both shared and distinct monocyte gene expression features: Women's Interagency HIV study.
title_fullStr HIV infection and cardiovascular disease have both shared and distinct monocyte gene expression features: Women's Interagency HIV study.
title_full_unstemmed HIV infection and cardiovascular disease have both shared and distinct monocyte gene expression features: Women's Interagency HIV study.
title_short HIV infection and cardiovascular disease have both shared and distinct monocyte gene expression features: Women's Interagency HIV study.
title_sort hiv infection and cardiovascular disease have both shared and distinct monocyte gene expression features women s interagency hiv study
url https://doi.org/10.1371/journal.pone.0285926
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