The Role of the Immunogenetic Background in the Development and Recurrence of Acute Idiopathic Pericarditis
2011; Karger Publishers; Volume: 118; Issue: 1 Linguagem: Inglês
10.1159/000324309
ISSN1421-9751
AutoresGeorge Lazaros, Apostolos Karavidas, M. Spyropoulou, Dimitris Tsiachris, Antonios Halapas, Achilleas Zacharoulis, Sophia Arapi, Vasiliki Matzaraki, Kostantinos Papadopoulos, Dimitrios Korres, Aliki Iniotaki, Vlassis N Pyrgakis, Christodoulos Stefanadis,
Tópico(s)Myasthenia Gravis and Thymoma
ResumoWe assessed the role of the immunogenetic background in the development and recurrence of acute idiopathic pericarditis (AIP).Fifty-five patients with a first episode of AIP were followed for 23.8 ± 6.3 months and recurrences were recorded. The control group consisted of 246 healthy individuals. In all subjects, genomic human leukocyte antigen (HLA) typing was performed. Moreover, circulating lymphocyte subpopulations were studied in 44 randomly selected patients and in 20 controls.An increased frequency of HLA-A*02, -Cw*07 and -DQB1*0202 alleles, and a decreased frequency of the -DQB1*0302 allele was detected in patients with AIP. The recurrence rate was 40% and time to recurrence was 202.8 ± 164.1 days. In patients with idiopathic recurrent pericarditis (RP), increased frequencies of HLA-A*02, -Cw*07 and -DQB1*0202 alleles were found. Notably, no patient with RP exhibited HLA-DRB1*04 and -DQB1*0302 alleles. Patients with RP exhibited lower CD4+/CD45RA+ naïve T cells (p = 0.03) than controls, and higher CD8+DR+ activated T cells (p = 0.01) than patients without recurrence and controls.HLA alleles may confer either susceptibility or resistance to AIP and RP. Circulating T-cell subpopulations may also predict RP. A combination of the above parameters might help to better define patients prone to recurrence.
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