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Age-Associated Changes in Monocyte and Innate Immune Activation Markers Occur More Rapidly in HIV Infected Women
Age-Associated Changes in Monocyte and Innate Immune Activation Markers Occur More Rapidly in HIV Infected Women
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Age-Associated Changes in Monocyte and Innate Immune Activation Markers Occur More Rapidly in HIV Infected Women
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Age-Associated Changes in Monocyte and Innate Immune Activation Markers Occur More Rapidly in HIV Infected Women
Age-Associated Changes in Monocyte and Innate Immune Activation Markers Occur More Rapidly in HIV Infected Women

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Age-Associated Changes in Monocyte and Innate Immune Activation Markers Occur More Rapidly in HIV Infected Women
Age-Associated Changes in Monocyte and Innate Immune Activation Markers Occur More Rapidly in HIV Infected Women
Journal Article

Age-Associated Changes in Monocyte and Innate Immune Activation Markers Occur More Rapidly in HIV Infected Women

2013
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Overview
Aging is associated with immune dysfunction and the related development of conditions with an inflammatory pathogenesis. Some of these immune changes are also observed in HIV infection, but the interaction between immune changes with aging and HIV infection are unknown. Whilst sex differences in innate immunity are recognized, little research into innate immune aging has been performed on women. This cross-sectional study of HIV positive and negative women used whole blood flow cytometric analysis to characterize monocyte and CD8(+) T cell subsets. Plasma markers of innate immune activation were measured using standard ELISA-based assays. HIV positive women exhibited elevated plasma levels of the innate immune activation markers CXCL10 (p<0.001), soluble CD163 (sCD163, p = 0.001), sCD14 (p = 0.022), neopterin (p = 0.029) and an increased proportion of CD16(+) monocytes (p = 0.009) compared to uninfected controls. Levels of the innate immune aging biomarkers sCD163 and the proportion of CD16(+) monocytes were equivalent to those observed in HIV negative women aged 14.5 and 10.6 years older, respectively. CXCL10 increased with age at an accelerated rate in HIV positive women (p = 0.002) suggesting a synergistic effect between HIV and aging on innate immune activation. Multivariable modeling indicated that age-related increases in innate immune biomarkers CXCL10 and sCD163 are independent of senescent changes in CD8(+) T lymphocytes. Quantifying the impact of HIV on immune aging reveals that HIV infection in women confers the equivalent of a 10-14 year increase in the levels of innate immune aging markers. These changes may contribute to the increased risk of inflammatory age-related diseases in HIV positive women.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject

Acquired immune deficiency syndrome

/ Adult

/ Age

/ Age Factors

/ Aging

/ Aging - immunology

/ AIDS

/ Analysis

/ Antigens, CD - blood

/ Antigens, Differentiation, Myelomonocytic - blood

/ Bioindicators

/ Biology

/ Biomarkers

/ Biomarkers - blood

/ Blood flow

/ Cardiovascular disease

/ Care and treatment

/ Case-Control Studies

/ CD16 antigen

/ CD163 antigen

/ CD8 antigen

/ CD8-Positive T-Lymphocytes - immunology

/ CD8-Positive T-Lymphocytes - pathology

/ Cell activation

/ Chemokine CXCL10 - blood

/ Cross-Sectional Studies

/ CXCL10 protein

/ Diagnosis

/ Enzyme-linked immunosorbent assay

/ Equivalence

/ Fc receptors

/ Female

/ Flow cytometry

/ Gender aspects

/ Gender differences

/ GPI-Linked Proteins - immunology

/ Health risks

/ HIV

/ HIV - immunology

/ HIV infections

/ HIV Infections - immunology

/ HIV Infections - pathology

/ HIV Infections - virology

/ Hospitals

/ Human immunodeficiency virus

/ Humans

/ Immune response

/ Immune system

/ Immunity

/ Immunity, Innate

/ Immunology

/ Immunophenotyping

/ Infections

/ Infectious diseases

/ Innate immunity

/ Lipopolysaccharide Receptors - blood

/ Lymphocytes

/ Lymphocytes T

/ Males

/ Medicine

/ Middle Aged

/ Monocytes

/ Monocytes - immunology

/ Monocytes - pathology

/ Neopterin

/ Neopterin - blood

/ Pathogenesis

/ Plasma levels

/ Receptors, Cell Surface - blood

/ Receptors, IgG - immunology

/ Sex differences

/ Sexes

/ Sexually transmitted diseases

/ STD

/ Studies

/ Synergistic effect

/ T cell receptors

/ T cells

/ Virology

/ Womens health