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https://www.arca.fiocruz.br/handle/icict/33009
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ArtigoDireito Autoral
Acesso restrito
Data de embargo
2050-01-01
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HLA-G IS EXPRESSED IN INTESTINAL SAMPLES OF ULCERATIVE COLITIS AND CROHN'S DISEASE PATIENTS AND HLA-G5 EXPRESSION IS DIFFERENTIALLY CORRELATED WITH TNF AND IL-10 CYTOKINE EXPRESSION
HLA-G
IL-10
Inflammatory bowel disease
TNF
Ulcerative colitis
Adulto
Envelhecido
Colite Ulcerativa / imunologia
Doença de Crohn / imunologia
Progressão da doença
Células Epiteliais / fisiologia
Fêmea
Antígenos HLA-G / metabolismo
Humanos
Imunohistoquímica
Imunomodulação
Interleucina-10 / genética
Interleucina-10 / metabolismo
Mucosa Intestinal / metabolismo
Intestinos / patologia
Masculino
Meia idade
Reação em Cadeia da Polimerase
RNA, mensageiro / análise
Fator alfa de necrose tumoral / genética
Fator de Necrose Tumoral alfa / metabolismo
Adulto jovem
Autor(es)
Afiliação
Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Recife, PE, Brasil.
Federal University of Pernambuco. School of Medicine. Department of Internal Medicine. Recife, PE, Brazil.
Federal University of Pernambuco. School of Medicine. Department of Internal Medicine. Recife, PE, Brazil.
Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Recife, PE, Brasil.
Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Recife, PE, Brasil.
Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Recife, PE, Brasil.
Federal University of Rio Grande do Norte. Department of Pharmacology. Natal, RN, Brazil.
Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Recife, PE, Brasil.
University of São Paulo. Medical School of Ribeirão Preto. Department of Internal Medicine. Ribeirão Preto, SP, Brazil.
Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Recife, PE, Brasil.
Federal University of Pernambuco. School of Medicine. Department of Internal Medicine. Recife, PE, Brazil.
Federal University of Pernambuco. School of Medicine. Department of Internal Medicine. Recife, PE, Brazil.
Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Recife, PE, Brasil.
Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Recife, PE, Brasil.
Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Recife, PE, Brasil.
Federal University of Rio Grande do Norte. Department of Pharmacology. Natal, RN, Brazil.
Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Recife, PE, Brasil.
University of São Paulo. Medical School of Ribeirão Preto. Department of Internal Medicine. Ribeirão Preto, SP, Brazil.
Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Recife, PE, Brasil.
Resumo em Inglês
HLA-G is an immunomodulatory molecule that can be produced by epithelial cells. Considering that TNF and IL-10 participate in bowel inflammatory disorders and that both cytokines modulate HLA-G, we evaluated HLA-G, TNF and IL-10 mRNA expression by qPCR and HLA-G protein levels by immunohistochemistry in two intestinal samples exhibiting different degree of inflammation within a patient suffering from Crohn's disease (CD) or ulcerative colitis (UC). Tissue HLA-G5 (P < 0.0001), TNF (P = 0.0004) and IL-10 (P = 0.0169) mRNA expression levels were higher in intestinal areas exhibiting intense inflammation compared to areas of low inflammation, and HLA-G protein levels were not associated with degree of mucosal inflammation. In CD, the expression of TNF was correlated with IL-10 in low inflamed areas, exhibiting a TNF:IL-10 ratio = 3, but in inflamed areas the ratio increased to 9-folds. In UC, the expression of TNF was correlated to IL-10, irrespective of the inflammation grade, with little variation of the TNF:IL-10 ratio in the various inflamed areas. TNF and IL-10 expression was correlated with HLA-G5 expression in mild inflamed areas. Both CD and UC samples exhibited gene and protein expression of HLA-G; and the HLA-G5 expression is differentially correlated with TNF and IL-10 levels depending on the type of the underlying inflammatory bowel disorder.
Palavras-chave em inglês
Crohn’s diseaseHLA-G
IL-10
Inflammatory bowel disease
TNF
Ulcerative colitis
DeCS
AdolescenteAdulto
Envelhecido
Colite Ulcerativa / imunologia
Doença de Crohn / imunologia
Progressão da doença
Células Epiteliais / fisiologia
Fêmea
Antígenos HLA-G / metabolismo
Humanos
Imunohistoquímica
Imunomodulação
Interleucina-10 / genética
Interleucina-10 / metabolismo
Mucosa Intestinal / metabolismo
Intestinos / patologia
Masculino
Meia idade
Reação em Cadeia da Polimerase
RNA, mensageiro / análise
Fator alfa de necrose tumoral / genética
Fator de Necrose Tumoral alfa / metabolismo
Adulto jovem
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