Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros











Base de dados
Tipo de estudo
Intervalo de ano de publicação
1.
Clin Immunol ; 96(2): 162-7, 2000 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-10900163

RESUMO

Deficiencies of factor I and/or factor H result in an increased consumption of C3 and higher susceptibility to recurrent infections. Here we describe a case of human factor I deficiency and lowered factor H levels. C3 concentration was 50% lower than normal, the classical pathway-dependent hemolytic activity was reduced to almost 30% of normal, and alternative pathway-dependent activity was completely absent. The killing by peripheral leukocytes of Candida albicans treated with deficient serum and the production of complement-dependent chemotactic factors were reduced in the proband's serum when compared with normal serum. Finally, we observed that C3 antigen present in the proband's serum has a different electrophoretic mobility than native C3 (most likely C3b), confirming the deregulation of complement activation due to the lack of regulatory proteins factors I and H. The impaired complement system described in this case, the first of its kind described in a Chile, explains the higher susceptibility to infections found in the proband.


Assuntos
Fator H do Complemento/metabolismo , Fator I do Complemento/deficiência , Animais , Fatores Quimiotáticos/biossíntese , Quimiotaxia , Criança , Pré-Escolar , Complemento C3/análise , Complemento C3b , Via Alternativa do Complemento/fisiologia , Via Clássica do Complemento/fisiologia , Eritrócitos , Feminino , Cobaias , Humanos , Imunoeletroforese , Masculino
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA