Your browser doesn't support javascript.
loading
Astute Clinician Report: A Novel 10 bp Frameshift Deletion in Exon 2 of ICOS Causes a Combined Immunodeficiency Associated with an Enteritis and Hepatitis.
Robertson, Nic; Engelhardt, Karin R; Morgan, Neil V; Barge, Dawn; Cant, Andrew J; Hughes, Stephen M; Abinun, Mario; Xu, Yaobo; Koref, Mauro Santibanez; Arkwright, Peter D; Hambleton, Sophie.
Afiliação
  • Robertson N; Primary Immunodeficiency Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.
  • Engelhardt KR; Great North Children's Hospital, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
  • Morgan NV; Primary Immunodeficiency Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.
  • Barge D; Centre for Cardiovascular Sciences, School of Clinical and Experimental Medicine, University of Birmingham, Birmingham, UK.
  • Cant AJ; Blood Sciences Flow Cytometry Laboratory, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
  • Hughes SM; Great North Children's Hospital, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
  • Abinun M; Paediatric Immunology, Royal Manchester Children's Hospital, Manchester, UK.
  • Xu Y; Great North Children's Hospital, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
  • Koref MS; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
  • Arkwright PD; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
  • Hambleton S; Paediatric Immunology, Royal Manchester Children's Hospital, Manchester, UK.
J Clin Immunol ; 35(7): 598-603, 2015 Oct.
Article em En | MEDLINE | ID: mdl-26399252
ICOS encodes the Inducible T-cell Co-Stimulator (ICOS). Deficiency of this receptor in humans causes a common variable immunodeficiency (CVID) characterised by an absence of class-switched memory B cells and hypogammaglobulinemia. Three pathogenic mutations in ICOS have been described to date in a total of 13 cases. Here we report a novel homozygous 10 base pair frameshift deletion in exon 2 discovered by whole exome sequencing of two siblings from a family of Pakistani origin. Both patients presented in early childhood with diarrhea, colitis and transaminitis and one showed defective handling of human herpesvirus 6. Activated patient CD3(+)CD4(+) T lymphocytes demonstrated a complete absence of ICOS expression and, consistent with previous reports, we detected a reduction in circulating T follicular helper cells. Findings in this kindred emphasise the phenotypic variability of ICOS deficiency and, in particular, the variably impaired antiviral immunity that is a poorly understood facet of this rare disorder.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos T Auxiliares-Indutores / Herpesvirus Humano 6 / Infecções por Roseolovirus / Enterite / Proteína Coestimuladora de Linfócitos T Induzíveis / Hepatite / Síndromes de Imunodeficiência Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: J Clin Immunol Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos T Auxiliares-Indutores / Herpesvirus Humano 6 / Infecções por Roseolovirus / Enterite / Proteína Coestimuladora de Linfócitos T Induzíveis / Hepatite / Síndromes de Imunodeficiência Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: J Clin Immunol Ano de publicação: 2015 Tipo de documento: Article