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克罗恩病:先天性免疫缺陷?

Crohn's disease: innate immunodeficiency?

作者信息

Yamamoto-Furusho Jesus-K, Korzenik Joshua-R

机构信息

Gastrointestinal Unit, Massachusetts General Hospital, 55 Fruit Street, Boston, Massachusetts 02114, USA.

出版信息

World J Gastroenterol. 2006 Nov 14;12(42):6751-5. doi: 10.3748/wjg.v12.i42.6751.

Abstract

In the past, Crohn's disease (CD) has been understood primarily as an immunologic disorder characterized by an abnormal T-cell response. Recent in vitro and in vivo data suggests that CD may instead be precipitated by innate immune dysfunction resulting from a combination of genetic and environmental factors. Some reports have demonstrated a defective immune response in a variety of other cellular components, including neutrophils, monocytes and dendritic cells. Recent studies of granulocyte-macrophage colony-stimulating factor (GM-CSF) in CD, aiming to stimulate the innate immune system with the conception that an innate immune defect underlies the development of the disease, have been demonstrated a clinical benefit and reinforce this evolving understanding of the disease.

摘要

过去,克罗恩病(CD)主要被理解为一种以异常T细胞反应为特征的免疫紊乱疾病。最近的体外和体内数据表明,CD可能反而由遗传和环境因素共同导致的固有免疫功能障碍引发。一些报告已证实在包括中性粒细胞、单核细胞和树突状细胞在内的多种其他细胞成分中存在免疫反应缺陷。最近针对CD中粒细胞巨噬细胞集落刺激因子(GM-CSF)的研究,旨在通过认为固有免疫缺陷是该疾病发展基础的理念来刺激固有免疫系统,已证明具有临床益处,并强化了对该疾病这种不断演变的认识。

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