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Relationships between phenotype and function of blood cd4+ t-cells and ascending thoracic aortic aneurysm: an experimental study
Sbrana, Silverio; Tiwari, Kaushal Kishore; Bevilacqua, Stefano; Giungato, Paola; Kallushi, Enkel; Solinas, Marco; Mazzone, Anna Maria.
  • Sbrana, Silverio; CNR Institute of Clinical Physiology. Flow Cytometry Laboratory. Massa. IT
  • Tiwari, Kaushal Kishore; "G. Monasterio" Foundation. "G. Pasquinucci" Heart Hospital. Cardiac Surgery Department. Massa. IT
  • Bevilacqua, Stefano; "G. Monasterio" Foundation. "G. Pasquinucci" Heart Hospital. Cardiac Surgery Department. Massa. IT
  • Giungato, Paola; CNR Institute of Biomedical Technologies. Cellular Biology Laboratory. Pisa. IT
  • Kallushi, Enkel; "G. Monasterio" Foundation. "G. Pasquinucci" Heart Hospital. Cardiac Surgery Department. Massa. IT
  • Solinas, Marco; "G. Monasterio" Foundation. "G. Pasquinucci" Heart Hospital. Cardiac Surgery Department. Massa. IT
  • Mazzone, Anna Maria; "G. Monasterio" Foundation. "G. Pasquinucci" Heart Hospital. Cardiology Department. Massa. IT
Rev. bras. cir. cardiovasc ; 34(1): 8-16, Jan.-Feb. 2019. tab, graf
Article in English | LILACS | ID: biblio-985250
ABSTRACT
Abstract

Introduction:

Non-familial ascending thoracic aorta dilation and aneurysms (TAAs) are silent diseases in elderly patients. Histopathology revealed that functionally polarized infiltrating CD4+ T-cells play a key role in aortic wall weakening.

Objective:

To evaluate the possible associations between phenotype and cytokine production of circulating CD4+ T-lymphocytes and the presence of TAA in patients with aortic valve disease (AVD).

Methods:

We studied blood samples from 10 patients with TAA and 10 patients with AVD. Flow cytometry was used to quantify a) CD4+ T-lymphocytes surface expression of CD25, CD28, and chemokine receptors (CCR5, CXCR3, CX3CR1); b) fractions of in vitro stimulated CD4+ T-cells producing cytokines (interferon gamma [IFN-γ], interleukin [IL]-17A, IL-21, IL-10); c) CD4+CD25highFoxP3+ regulatory T-cells (Treg) fraction. Enzyme-linked immunosorbent assays (ELISA) were performed for cytokines (IFN-γ, IL-6, IL-10, IL-17A, IL-23, transforming growth factor beta [TGF-β]) and chemokines (RANTES, CX3CL1).

Results:

The total CD4+CD28±CD4+/CX3CR1+ T-cells fraction was higher (P=0.0323) in AVD (20.452±4.673) than in TAA patients (8.633±2.030). The frequency ratio of CD4+ T-lymphocytes producing IFN-γ vs. IL-17A+IL-21 cytokine-producing CD4+ T-cells was higher (P=0.0239) in AVD (2.102±0.272) than in TAA (1.365±0.123) patients. The sum of CD4+CD28±CD4+/CX3CR1+ T-cells correlated positively with values of the previous cytokine ratio (P=0.0002, R=0.732). The ratio of CD4+CD28±CD4+/CX3CR1+ T-cells vs. Treg was higher (P=0.0008) in AVD (20.859±3.393) than in TAA (6.367±1.277) patients.

Conclusion:

Our results show that the presence of TAA in subjects with AVD is associated with imbalance between phenotypic and cytokine-producing subsets of circulating CD4+ T-lymphocytes, prevalently oriented towards a pro-fibrotic and IFN-γ counteracting effect to functional polarization.
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Aortic Valve / Phenotype / CD4-Positive T-Lymphocytes / Cytokines / Aortic Aneurysm, Thoracic / Heart Valve Diseases Limits: Aged / Female / Humans / Male Language: English Journal: Rev. bras. cir. cardiovasc Journal subject: Cardiology / General Surgery Year: 2019 Type: Article Affiliation country: Italy Institution/Affiliation country: "G. Monasterio" Foundation/IT / CNR Institute of Biomedical Technologies/IT / CNR Institute of Clinical Physiology/IT

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Full text: Available Index: LILACS (Americas) Main subject: Aortic Valve / Phenotype / CD4-Positive T-Lymphocytes / Cytokines / Aortic Aneurysm, Thoracic / Heart Valve Diseases Limits: Aged / Female / Humans / Male Language: English Journal: Rev. bras. cir. cardiovasc Journal subject: Cardiology / General Surgery Year: 2019 Type: Article Affiliation country: Italy Institution/Affiliation country: "G. Monasterio" Foundation/IT / CNR Institute of Biomedical Technologies/IT / CNR Institute of Clinical Physiology/IT