Loss of Interleukin-10 Signaling and Infantile Inflammatory Bowel Disease: Implications for Diagnosis and Therapy
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
29/10/2013
29/10/2013
2012
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Resumo |
BACKGROUND & AIMS: Homozygous loss of function mutations in interleukin-10 (IL10) and interleukin-10 receptors (IL10R) cause severe infantile (very early onset) inflammatory bowel disease (IBD). Allogeneic hematopoietic stem cell transplantation (HSCT) was reported to induce sustained remission in 1 patient with IL-10R deficiency. We investigated heterogeneity among patients with very early onset IBD, its mechanisms, and the use of allogeneic HSCT to treat this disorder. METHODS: We analyzed 66 patients with early onset IBD (younger than 5 years of age) for mutations in the genes encoding IL-10, IL-10R1, and IL-10R2. IL-10R deficiency was confirmed by functional assays on patients' peripheral blood mononuclear cells (immunoblot and enzyme-linked immunosorbent assay analyses). We assessed the therapeutic effects of standardized allogeneic HSCT. RESULTS: Using a candidate gene sequencing approach, we identified 16 patients with IL-10 or IL-10R deficiency: 3 patients had mutations in IL-10, 5 had mutations in IL-10R1, and 8 had mutations in IL-10R2. Refractory colitis became manifest in all patients within the first 3 months of life and was associated with perianal disease (16 of 16 patients). Extraintestinal symptoms included folliculitis (11 of 16) and arthritis (4 of 16). Allogeneic HSCT was performed in 5 patients and induced sustained clinical remission with a median follow-up time of 2 years. In vitro experiments confirmed reconstitution of IL-10R-mediated signaling in all patients who received the transplant. CONCLUSIONS: We identified loss of function mutations in IL-10 and IL-10R in patients with very early onset IBD. These findings indicate that infantile IBD patients with perianal disease should be screened for IL-10 and IL-10R deficiency and that allogeneic HSCT can induce remission in those with IL-10R deficiency. DFG DFG [SFB621] Deutsche Jose Carreras LeukamieStiftung e. V. Deutsche Jose Carreras Leukamie-Stiftung e. V. BMBF (ERARE) BMBF (E-RARE) Care-for-Rare Foundation CareforRare Foundation |
Identificador |
GASTROENTEROLOGY, PHILADELPHIA, v. 143, n. 2, supl. 5, Part 3, pp. 347-355, AUG, 2012 0016-5085 http://www.producao.usp.br/handle/BDPI/36166 10.1053/j.gastro.2012.04.045 |
Idioma(s) |
eng |
Publicador |
W B SAUNDERS CO-ELSEVIER INC PHILADELPHIA |
Relação |
GASTROENTEROLOGY |
Direitos |
closedAccess Copyright W B SAUNDERS CO-ELSEVIER INC |
Palavras-Chave | #CHILDREN #GENETIC DEFECT #IMMUNODEFICIENCY #INTESTINAL INFLAMMATION #STEM-CELL TRANSPLANTATION #BONE-MARROW-TRANSPLANTATION #GENOME-WIDE ASSOCIATION #REFRACTORY CROHNS-DISEASE #NON-HODGKINS-LYMPHOMA #COMPLETE REMISSION #RECEPTOR #PATHOGENESIS #LEUKEMIA #COLITIS #GASTROENTEROLOGY & HEPATOLOGY |
Tipo |
article original article publishedVersion |