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J Immunol ; 192(10): 4897-912, 2014 May 15.
Article in English | MEDLINE | ID: mdl-24752442

ABSTRACT

Abdominal aortic aneurysm (AAA) is a common disease with often life-threatening consequences. This vascular disorder is responsible for 1-2% of all deaths in men aged 65 years or older. Autoimmunity may be responsible for the pathogenesis of AAA. Although it is well documented that infiltrating T cells are essentially always present in AAA lesions, little is known about their role in the initiation and/or progression of the disease. To determine whether T cells infiltrating AAA lesions contain clonally expanded populations of T cells, we amplified ß-chain TCR transcripts by the nonpalindromic adaptor-PCR/Vß-specific PCR and/or Vß-specific PCR, followed by cloning and sequencing. We report in this article that aortic abdominal aneurysmal lesions from 8 of 10 patients with AAA contained oligoclonal populations of T cells. Multiple identical copies of ß-chain TCR transcripts were identified in these patients. These clonal expansions are statistically significant. These results demonstrate that αß TCR(+) T lymphocytes infiltrating aneurysmal lesions of patients with AAA have undergone proliferation and clonal expansion in vivo at the site of the aneurysmal lesion, in response to unidentified self- or nonself Ags. This evidence supports the hypothesis that AAA is a specific Ag-driven T cell disease.


Subject(s)
Aortic Aneurysm, Abdominal/immunology , Cell Proliferation , Clonal Selection, Antigen-Mediated , Receptors, Antigen, T-Cell, alpha-beta/immunology , T-Lymphocytes/immunology , Aged , Aged, 80 and over , Aortic Aneurysm, Abdominal/pathology , Female , Humans , Male , Middle Aged , T-Lymphocytes/pathology
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