Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/200496
Type: Artigo de periódico
Title: Characterization Of Cd4+cd28null T Cells In Patients With Coronary Artery Disease And Individuals With Risk Factors For Atherosclerosis.
Author: Téo, Fábio Haach
de Oliveira, Rômulo Tadeu Dias
Mamoni, Ronei Luciano
Ferreira, Maria Carolina Salmora
Nadruz, Wilson
Coelho, Otávio Rizzi
Fernandes, Juliano de Lara
Blotta, Maria Heloisa Souza Lima
Abstract: Risk factors for atherosclerosis may contribute to chronic low-grade inflammation. A highly cytotoxic and inflammatory CD4(+) cell subset (CD4(+)CD28(null) cells) has been associated with inflammatory diseases, including acute coronary syndromes (ACS). The aim of this study was to quantify and characterize CD4(+)CD28(null) cells in individuals with risk factors for atherosclerosis and patients with coronary artery disease (CAD). In order to achieve this goal, peripheral blood mononuclear cells (PBMCs) from individuals with risk factors for atherosclerosis and patients with CAD were analyzed using flow cytometry to detect cytotoxic molecules and evaluate the expression of homing receptors and inflammatory cytokines in CD4(+) cell subsets. The cells were evaluated ex vivo and after stimulation in culture. We found no differences in the proportions of CD4(+)CD28(null) cells among the groups. Compared with the CD4(+)CD28(+) population, the ex vivo CD4(+)CD28(null) subset from all groups expressed higher levels of granzymes A and B, perforin, granulysin and interferon-γ (IFN-γ). Individuals with risk factors and patients with ACS showed the highest levels of cytotoxic molecules. After stimulation, tumor necrosis factor-α (TNF-α) expression in the CD4(+)CD28(null) subset from these groups increased more than in the other groups. Stimulation with LPS decreased the expression of cytotoxic molecules by CD4(+)CD28(null) cells in all groups. In conclusion, our results show that risk factors for atherosclerosis may alter the CD4(+)CD28(null) cells phenotype, increasing their cytotoxic potential. Our findings also suggest that CD4(+)CD28(null) cells may participate in the early phases of atherosclerosis.
Subject: Adult
Aged
Aged, 80 And Over
Antigens, Cd28
Antigens, Differentiation, T-lymphocyte
Atherosclerosis
Cd4-positive T-lymphocytes
Coronary Artery Disease
Female
Granzymes
Humans
Interferon-gamma
Leukocytes, Mononuclear
Lipopolysaccharides
Male
Middle Aged
Perforin
Receptors, Ccr7
Receptors, Cxcr3
Risk Factors
T-lymphocyte Subsets
Tumor Necrosis Factor-alpha
Rights: fechado
Identifier DOI: 10.1016/j.cellimm.2013.01.007
Address: http://www.ncbi.nlm.nih.gov/pubmed/23416719
Date Issue: 2013
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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