TY - JOUR
T1 - Phenotypic and functional alterations on inflammatory peripheral blood cells after acute myocardial infarction
AU - Carvalheiro, Tiago
AU - Velada, Isabel
AU - Valado, Ana
AU - Mendes, Fernando
AU - Martinho, António
AU - António, Natália
AU - Gonçalves, Lino
AU - Providência, Luís
AU - Pais, Maria Luísa
AU - Paiva, Artur
PY - 2012/6
Y1 - 2012/6
N2 - The frequency and function of T cells, monocytes, and dendritic cell subsets were investigated in 12 patients after acute myocardial infarction (AMI)-(T0), 1 month after the episode (T1), and in 12 healthy individuals (HG). The cell characterization and the functional studies were performed by flow cytometry and by RT-PCR, after cell sorting. The most important findings at T0 moment, when compared with T1 and HG, were: a decrease in the frequency of IL-2-producing T cells; a lower frequency of TNF-α- and IL-6-producing monocytes, myeloid dendritic cells, and CD14(-/low)CD16(+)DCs; and a lower TNF-α mRNA expression, after sorting these cells. Moreover, the regulatory function of Treg cells, at T0 moment, was upregulated, based on the FoxP3, CTLA-4, and TGF-β mRNA expression increase. The majority of these phenotypic and functional alterations disappeared at T1. Our data demonstrate that AMI induces a significant change in the immune system homeostasis.
AB - The frequency and function of T cells, monocytes, and dendritic cell subsets were investigated in 12 patients after acute myocardial infarction (AMI)-(T0), 1 month after the episode (T1), and in 12 healthy individuals (HG). The cell characterization and the functional studies were performed by flow cytometry and by RT-PCR, after cell sorting. The most important findings at T0 moment, when compared with T1 and HG, were: a decrease in the frequency of IL-2-producing T cells; a lower frequency of TNF-α- and IL-6-producing monocytes, myeloid dendritic cells, and CD14(-/low)CD16(+)DCs; and a lower TNF-α mRNA expression, after sorting these cells. Moreover, the regulatory function of Treg cells, at T0 moment, was upregulated, based on the FoxP3, CTLA-4, and TGF-β mRNA expression increase. The majority of these phenotypic and functional alterations disappeared at T1. Our data demonstrate that AMI induces a significant change in the immune system homeostasis.
KW - Adult
KW - Aged
KW - Biomarkers/blood
KW - Case-Control Studies
KW - Cell Separation
KW - Dendritic Cells/immunology
KW - Female
KW - Flow Cytometry
KW - GPI-Linked Proteins/blood
KW - Humans
KW - Immunophenotyping
KW - Inflammation/blood
KW - Inflammation Mediators/blood
KW - Interleukin-2/blood
KW - Interleukin-6/blood
KW - Lipopolysaccharide Receptors/blood
KW - Male
KW - Middle Aged
KW - Monocytes/immunology
KW - Myocardial Infarction/blood
KW - Phenotype
KW - Portugal
KW - Prospective Studies
KW - RNA, Messenger/blood
KW - Real-Time Polymerase Chain Reaction
KW - Receptors, IgG/blood
KW - T-Lymphocyte Subsets/immunology
KW - Time Factors
KW - Tumor Necrosis Factor-alpha/blood
U2 - 10.1007/s12265-012-9365-8
DO - 10.1007/s12265-012-9365-8
M3 - Article
C2 - 22528677
SN - 1937-5387
VL - 5
SP - 309
EP - 320
JO - Journal of cardiovascular translational research
JF - Journal of cardiovascular translational research
IS - 3
ER -