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Characterization of CD4(+) T Cell Subsets in Patients with Abdominal Aortic Aneurysms

BACKGROUND: The mediators produced by CD4(+) T lymphocytes are involved in the pathogenesis of aneurysmal lesions in abdominal aortic aneurysm (AAA) patients. The aim of this study was to identify and characterize the CD4(+) T cell subsets involved in human AAA. METHODS: The CD4(+) T cell subsets in...

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Detalles Bibliográficos
Autores principales: Téo, Fábio Haach, de Oliveira, Rômulo Tadeu Dias, Villarejos, Liana, Mamoni, Ronei Luciano, Altemani, Albina, Menezes, Fabio Husemann, Blotta, Maria Heloisa Souza Lima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327259/
https://www.ncbi.nlm.nih.gov/pubmed/30686933
http://dx.doi.org/10.1155/2018/6967310
Descripción
Sumario:BACKGROUND: The mediators produced by CD4(+) T lymphocytes are involved in the pathogenesis of aneurysmal lesions in abdominal aortic aneurysm (AAA) patients. The aim of this study was to identify and characterize the CD4(+) T cell subsets involved in human AAA. METHODS: The CD4(+) T cell subsets in 30 human aneurysmal lesions were determined using flow cytometry (FC) and immunohistochemistry (IHC). The peripheral blood mononuclear cells (PBMCs) from patients with AAA were also analyzed by FC and compared with control subjects. RESULTS: Human aneurysmal lesions contained IFN-γ, IL-12p35, IL-4, IL-23p19, IL-17R, and IL-22 positive cells. PBMCs from AAA patients had higher expression levels of IFN-γ, TNF-α, IL-4, and IL-22 when compared to controls. CONCLUSIONS: Our results show the presence of T(H)1, T(H)2, T(H)17, and T(H)22 subsets in aneurysmal lesions of AAA patients and suggest that these cells may be mainly activated in situ, where they can induce tissue degradation and contribute to the pathogenesis of AAA.