Increased glucose transporter-1 expression on intermediate monocytes from HIV-infected women with subclinical cardiovascular disease. (14th January 2017)
- Record Type:
- Journal Article
- Title:
- Increased glucose transporter-1 expression on intermediate monocytes from HIV-infected women with subclinical cardiovascular disease. (14th January 2017)
- Main Title:
- Increased glucose transporter-1 expression on intermediate monocytes from HIV-infected women with subclinical cardiovascular disease
- Authors:
- Butterfield, Tiffany R.
Hanna, David B.
Kaplan, Robert C.
Kizer, Jorge R.
Durkin, Helen G.
Young, Mary A.
Nowicki, Marek J.
Tien, Phyllis C.
Golub, Elizabeth T.
Floris-Moore, Michelle A.
Titanji, Kehmia
Fischl, Margaret A.
Heath, Sonya L.
Martinson, Jefferey
Crowe, Suzanne M.
Palmer, Clovis S.
Landay, Alan L.
Anzinger, Joshua J. - Abstract:
- Abstract : Objective: People living with HIV (PLWH) have chronic immune activation and increased cardiovascular disease (CVD) risk. Activation of monocytes and T lymphocytes causes upregulation of glucose transporter-1 (GLUT1) for efficient function. PLWH have an increased percentage of GLUT1-expressing monocytes and T lymphocytes, but it is unclear if these cells are associated with CVD. We evaluated the expression of GLUT1 and CD38 on monocyte and T lymphocyte populations from HIV-infected women with subclinical CVD. Methods: Participants with more than 75th percentile ( n = 15) and less than 25th percentile ( n = 15) age-adjusted intima-media thickness (IMT) at the right common carotid artery and bifurcation were identified from the Women's Interagency HIV Study. Groups were matched by age, race/ethnicity, smoking status, and CD4 + cell count. All women were receiving suppressive antiretroviral therapy except for one high and one low IMT participant. Monocyte and T lymphocyte populations were evaluated for GLUT1 and CD38 expression using flow cytometry. Results: Intermediate monocytes from high IMT women had significantly increased expression of GLUT1 (310 MFI vs. 210 MFI, P = 0.024 ) (66.4% vs. 48.5%, P = 0.031 ) and CD38 (339 MFI vs. 211 MFI, P = 0.002 ) (10.5% vs. 3.8%, P = 0.0002 ) compared with women with low IMT. High and low IMT participants showed no differences in GLUT1 or CD38 expression on classical monocytes, nonclassical monocytes, CD4 + andAbstract : Objective: People living with HIV (PLWH) have chronic immune activation and increased cardiovascular disease (CVD) risk. Activation of monocytes and T lymphocytes causes upregulation of glucose transporter-1 (GLUT1) for efficient function. PLWH have an increased percentage of GLUT1-expressing monocytes and T lymphocytes, but it is unclear if these cells are associated with CVD. We evaluated the expression of GLUT1 and CD38 on monocyte and T lymphocyte populations from HIV-infected women with subclinical CVD. Methods: Participants with more than 75th percentile ( n = 15) and less than 25th percentile ( n = 15) age-adjusted intima-media thickness (IMT) at the right common carotid artery and bifurcation were identified from the Women's Interagency HIV Study. Groups were matched by age, race/ethnicity, smoking status, and CD4 + cell count. All women were receiving suppressive antiretroviral therapy except for one high and one low IMT participant. Monocyte and T lymphocyte populations were evaluated for GLUT1 and CD38 expression using flow cytometry. Results: Intermediate monocytes from high IMT women had significantly increased expression of GLUT1 (310 MFI vs. 210 MFI, P = 0.024 ) (66.4% vs. 48.5%, P = 0.031 ) and CD38 (339 MFI vs. 211 MFI, P = 0.002 ) (10.5% vs. 3.8%, P = 0.0002 ) compared with women with low IMT. High and low IMT participants showed no differences in GLUT1 or CD38 expression on classical monocytes, nonclassical monocytes, CD4 + and CD8 + T lymphocytes. Conclusion: GLUT1-expressing intermediate monocytes are elevated in HIV-infected women with subclinical CVD. These cells may contribute to development of CVD in PLWH and could be a novel target to limit inflammation. Abstract : Supplemental Digital Content is available in the text … (more)
- Is Part Of:
- AIDS. Volume 31:Number 2(2017)
- Journal:
- AIDS
- Issue:
- Volume 31:Number 2(2017)
- Issue Display:
- Volume 31, Issue 2 (2017)
- Year:
- 2017
- Volume:
- 31
- Issue:
- 2
- Issue Sort Value:
- 2017-0031-0002-0000
- Page Start:
- Page End:
- Publication Date:
- 2017-01-14
- Subjects:
- cardiovascular disease -- GLUT1 -- HIV -- monocyte -- T cell
AIDS (Disease) -- Periodicals
Acquired Immunodeficiency Syndrome
AIDS (Disease)
Periodicals
Periodicals
616.9792005 - Journal URLs:
- http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&PAGE=toc&D=ovft&AN=00002030-000000000-00000 ↗
http://journals.lww.com/aidsonline/pages/default.aspx?desktopMode=true ↗
http://journals.lww.com/pages/default.aspx ↗ - DOI:
- 10.1097/QAD.0000000000001320 ↗
- Languages:
- English
- ISSNs:
- 0269-9370
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0773.083000
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British Library STI - ELD Digital store - Ingest File:
- 8240.xml