Association of γδ T cells with disease severity and mortality in septic patients

Gamma-delta T cells are the most abundant of all epithelial-resident lymphocytes and are considered a first line of defense against pathogens in the mucosa. Our objective was to confirm the reduction in γδ T cell subsets and its relationship with mortality in patients with sepsis. We studied 135 pat...

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Published in:Clinical and vaccine immunology Vol. 20; no. 5; p. 738
Main Authors: Andreu-Ballester, Juan C, Tormo-Calandín, Constantino, Garcia-Ballesteros, Carlos, Pérez-Griera, J, Amigó, Victoria, Almela-Quilis, Amadeo, Ruiz del Castillo, Juan, Peñarroja-Otero, Carlos, Ballester, Ferran
Format: Journal Article
Language:English
Published: United States 01.05.2013
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ISSN:1556-679X, 1556-679X
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Summary:Gamma-delta T cells are the most abundant of all epithelial-resident lymphocytes and are considered a first line of defense against pathogens in the mucosa. Our objective was to confirm the reduction in γδ T cell subsets and its relationship with mortality in patients with sepsis. We studied 135 patients with sepsis attended in the emergency department and intensive care unit of two hospitals and compared them with a similar control group of healthy subjects. The αβ and γδ T cell subsets were determined via flow cytometry according to the stage of the sepsis and its relationship with mortality. All the lymphocyte subsets were reduced with respect to the corresponding subsets in the control group. All the γδ T cell populations decreased significantly as the septic picture worsened. Furthermore, γδ T cells showed decreases at days 2, 3, and 4 from the start of sepsis. Twenty-six patients with sepsis died (19.3%). The γδ T cells, specifically, the CD3(+) CD56(+) γδ T cells, were significantly reduced in those septic patients who died. Our results indicate that, during sepsis, γδ T cells show the largest decrease and this reduction becomes more intense when the septic process becomes more severe. Mortality was associated with a significant decrease in γδ T cells.
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ISSN:1556-679X
1556-679X
DOI:10.1128/CVI.00752-12