Loss of Interleukin-10 Signaling and Infantile Inflammatory Bowel Disease: Implications for Diagnosis and Therapy


Autoria(s): Kotlarz, Daniel; Beier, Rita; Murugan, Dhaarini; Diestelhorst, Jana; Jensen, Ole; Boztug, Kaan; Pfeifer, Dietmar; Kreipe, Hans; Pfister, Eva-Doreen; Baumann, Ulrich; Puchalka, Jacek; Bohne, Jens; Egritas, Odul; Dalgic, Buket; Kolho, Kaija-Leena; Sauerbrey, Axel; Buderus, Stephan; Guengoer, Tayfun; Enninger, Axel; Ling Koda, Yu Kar; Guariso, Graziella; Weiss, Batia; Corbacioglu, Selim; Socha, Piotr; Uslu, Nuray; Metin, Ayse; Wahbeh, Ghassan T.; Husain, Khalid; Ramadan, Dina; Al-Herz, Waleed; Grimbacher, Bodo; Sauer, Martin; Sykora, Karl-Walter; Koletzko, Sibylle; Klein, Christoph
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

29/10/2013

29/10/2013

2012

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

http://dx.doi.org/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