Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/87982
Type: Artigo de periódico
Title: The Ccr5Δ32 Polymorphism In Brazilian Patients With Sickle Cell Disease
Author: Lopes M.P.
Santos M.N.N.
Faber E.W.
Bezerra M.A.C.
Hatzlhofer B.L.D.
Albuquerque D.M.
Zaccariotto T.R.
Ribeiro D.M.
Da Silva Araujo A.
Costa F.F.
De Fatima Sonati M.
Abstract: Background. Previous studies on the role of inflammation in the pathophysiology of sickle cell disease (SCD) suggested that the CCR5Δ32 allele, which is responsible for the production of truncated C-C chemokine receptor type 5 (CCR5), could confer a selective advantage on patients with SCD because it leads to a less efficient Th1 response. We determined the frequency of the CCR5Δ32 polymorphism in 795 Afro-Brazilian SCD patients followed up at the Pernambuco Hematology and Hemotherapy Center, in Northeastern Brazil, divided into a pediatric group (3 months-17 years, n = 483) and an adult group (18-70 years, n = 312). The adult patients were also compared to a healthy control group (blood donors, 18-61 years, n = 247). Methods. The CCR5/CCR5Δ32 polymorphism was determined by allele-specific PCR. Results. No homozygous patient for the CCR5Δ32 allele was detected. The frequency of heterozygotes in the study population (patients and controls) was 5.8%, in the total SCD patients 5.1%, in the children 5.4%, in the adults with SCD 4.8%, and in the adult controls 8.1%. These differences did not reach statistical significance. Conclusions. Our findings failed to demonstrate an important role of the CCR5Δ32 allele in the population sample studied here.
Editor: Hindawi Publishing Corporation
Rights: fechado
Identifier DOI: 10.1155/2014/678246
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-84918769756&partnerID=40&md5=bde7ac5a854eee99659c2ca3ec05a486
Date Issue: 2014
Appears in Collections:Unicamp - Artigos e Outros Documentos

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