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|Title: ||A remarkable depletion of both naïve CD4+ and CD8+ with high proportion of memory T cells in an IPEX infant with a FOXP3 mutation in the forkhead domain|
|Authors: ||Costa-Carvalho, B.T.|
de Moraes-Pinto, M.I.
de Almeida, L.C.
de Seixas Alves, M.T.
de Souza, R.L.
|Keywords: ||Determinantes Imunológicos em Doenças Crónicas|
|Issue Date: ||Jul-2008|
|Publisher: ||Blackwell Publishing|
|Citation: ||Scand J Immunol. 2008 Jul;68(1):85-91. Epub 2008 May 15|
|Abstract: ||IPEX is a rare X-linked syndrome, with immune dysfunction, polyendocrinopathy and enteropathy. We describe an infant who died at the age of 11 months after developing eczema, severe diarrhoea, diabetes, hypothyroidism, thrombocytopenia and four episodes of septicaemia. Immunophenotyping of peripheral blood at 8 months revealed normal CD3+ T, CD4+ T and CD8+ T cell numbers, with low NK and B cells. CD4+ and CD8+ T lymphocytes showed remarkably low numbers and percentages of naïve cells and high numbers of memory CD4 and CD8 cells. At autopsy, an intense depletion of immune cells in thymus, spleen and lymph nodes was observed. No Hassall's corpuscles were found in thymus. Lymphocytic pancreatitis and intense villous atrophy with mucosal lymphocytic infiltration in small bowel were also seen. FOXP3 gene studies revealed a: C-->G substitution 3 bp upstream of exon 10, which prevents splicing between exons 9 and 10, likely resulting in a functionally altered or deficient protein. Florid clinical findings are usually observed in association of forkhead DNA-binding domain mutations. The intense depletion of naïve T cells we report suggest that depletion of immune cells might take place due to uncontrolled activation due to the absence of regulatory T cells.|
|Peer Reviewed: ||yes|
|Publisher version: ||http://onlinelibrary.wiley.com/doi/10.1111/j.1365-3083.2008.02055.x/abstract?systemMessage=Wiley+Online+Library+will+be+disrupted+4+Feb+from+10-12+GMT+for+monthly+maintenance|
|Appears in Collections:||DPSPDNT - Artigos em revistas internacionais|
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