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结节病的免疫病理学

Immunopathology of sarcoidosis.

作者信息

Mortaz Esmaeil, Masjedi Mohammad Reza, Tabarsi Payam, Pourabdollah Mihan, Adcock Ian M

机构信息

Division of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Faculty of Science, Utrecht University, Utrecht, The Netherlands.

Respiratory Diseases Research Center and National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Department of Immunology, ShahidBeheshti University of Medical Sciences, Tehran, Iran.

出版信息

Iran J Allergy Asthma Immunol. 2014 Oct;13(5):300-6.

Abstract

The immunopathology of sarcoidosis remains elusive despite years of research into this multiorgan disease.However, recent studies have provided new insights into the genetics and immune components involved in the clinical manifestation of the disease. Granulomatous inflammation is due to the host immune response to a persistent poorly degradable unknown antigen.Mycobacterium tuberculosis (MTB) is the major disease driver in many patients. The immune mechanisms that cause this disease start with the antigenic stimulus, followed by T-cell, macrophage and dendritic cell activation via a classic MHC II-mediated pathway. In addition, the profile of immune mediators reported in sarcoidosis indicates that the inflammasome pathway plays a critical role in disease pathogenesis. Increased understanding of the signal transductions pathways involved in the induction of inflammatory processes in sarcoidosis could give rise to new therapeutic approaches in future.

摘要

尽管对这种多器官疾病进行了多年研究,结节病的免疫病理学仍不清楚。然而,最近的研究为该疾病临床表现中涉及的遗传学和免疫成分提供了新的见解。肉芽肿性炎症是由于宿主对持续存在的、难以降解的未知抗原的免疫反应。结核分枝杆菌(MTB)是许多患者的主要疾病驱动因素。导致这种疾病的免疫机制始于抗原刺激,随后通过经典的MHC II介导途径激活T细胞、巨噬细胞和树突状细胞。此外,结节病中报道的免疫介质谱表明,炎性小体途径在疾病发病机制中起关键作用。对结节病中炎症过程诱导所涉及的信号转导途径的进一步了解可能会在未来产生新的治疗方法。

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