Activation-induced Cell Death Drives Profound Lung CD4 + T-Cell Depletion in HIV-associated Chronic Obstructive Pulmonary Disease

As overall survival improves, individuals with HIV infection become susceptible to other chronic diseases, including accelerated chronic obstructive pulmonary disease (COPD). To determine whether individuals with HIV-associated COPD exhibit dysregulated lung mucosal T-cell immunity compared with con...

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Vydané v:American journal of respiratory and critical care medicine Ročník 190; číslo 7; s. 744 - 755
Hlavní autori: Popescu, Iulia, Drummond, M. Bradley, Gama, Lucio, Coon, Tiffany, Merlo, Christian A., Wise, Robert A., Clements, Janice E., Kirk, Gregory D., McDyer, John F.
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States American Thoracic Society 01.10.2014
Predmet:
Apoptosis - immunology
Bronchoalveolar Lavage Fluid - immunology
CD4-Positive T-Lymphocytes - immunology
CD8-Positive T-Lymphocytes - immunology
Cell Death
Cohort Studies
fas Receptor - immunology
Female
Flow Cytometry - methods
HIV Infections - complications
HIV Infections - immunology
Humans
Immunity, Mucosal - immunology
Leukocytes, Mononuclear - immunology
Longitudinal Studies
Lung - immunology
Male
Middle Aged
Original
Pulmonary Disease, Chronic Obstructive - complications
Pulmonary Disease, Chronic Obstructive - immunology
Viral Load - immunology
apoptosis
HIV
T cells
immune activation
COPD
ISSN:1073-449X, 1535-4970, 1535-4970
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Shrnutí:As overall survival improves, individuals with HIV infection become susceptible to other chronic diseases, including accelerated chronic obstructive pulmonary disease (COPD). To determine whether individuals with HIV-associated COPD exhibit dysregulated lung mucosal T-cell immunity compared with control subjects. Using flow cytometry, we evaluated peripheral blood and lung mucosal T-cell immunity in 14 HIV(+)COPD(+), 13 HIV(+)COPD(-), and 7 HIV(-)COPD(+) individuals. HIV(+)COPD(+) individuals demonstrated profound CD4(+) T-cell depletion with reduced CD4/CD8 T-cell ratios in bronchoalveolar lavage-derived lung mononuclear cells, not observed in peripheral blood mononuclear cells, and diminished CD4(+) T cell absolute numbers, compared with control subjects. Furthermore, HIV(+)COPD(+) individuals demonstrated decreased pulmonary HIV-specific and staphylococcal enterotoxin B-reactive CD4(+) memory responses, including loss of multifunctionality, compared with HIV(+)COPD(-) control subjects. In contrast, lung mucosal HIV-specific CD8(+) T-cell responses were preserved. Lung CD4(+) T cells from HIV(+)COPD(+) individuals expressed increased surface Fas death receptor (CD95) and programmed death-1, but similar bronchoalveolar lavage viral loads as control subjects. However, programmed death-1 expression inversely correlated with HIV-specific lung CD4(+)IFN-γ(+) T-cell responses, suggesting functional exhaustion. Moreover, lung CD4(+) T cells from HIV(+)COPD(+) patients demonstrated increased basal and HIV antigen-induced expression of the early apoptosis marker annexin V compared with control subjects, which was significantly attenuated with anti-Fas blockade. Lastly, lung mucosal, but not blood, CD4(+)/CD8(+) ratios from HIV(+) patients significantly correlated with the FEV1, but not in HIV(-)COPD(+) patients. Together, our results provide evidence for profound lung mucosal CD4(+) T-cell depletion via a Fas-dependent activation-induced cell death mechanism, along with impaired HIV-specific CD4(+) immunity as immunologic features of HIV-associated COPD.
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Both authors contributed equally to this work.
ISSN:1073-449X
1535-4970
1535-4970
DOI:10.1164/rccm.201407-1226OC