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系统性红斑狼疮1、2、3……狼疮的基因剖析

SLE 1, 2, 3...genetic dissection of lupus.

作者信息

Zhu Jiankun, Mohan Chandra

机构信息

Department of Internal Medicine, the Center for Immunology, University of Texas Southwestem Medical School, Dallas, TX, USA.

出版信息

Adv Exp Med Biol. 2007;601:85-95. doi: 10.1007/978-0-387-72005-0_9.

Abstract

Systemic lupus erythematosus (SLE) is a chronic and complex autoimmune disease of unknown etiology, characterized by the presence of widespread immunological abnormalities and multiorgan injury. An important advance over the past decade has been our understanding of how different genetic loci (or genes) may dictate specific immune abnormalities in lupus. "Genetic dissection" has unveiled some of the mystery enshrouding lupus pathogenesis. It appears that there are at least two distinct events leading to disease. The first involves a breach in the adaptive immune system and the second involves a dysregulation of innate immunity. Co-ordinate dysregulation of both checkpoints is necessary for full-blown lupus to ensue. The challenge ahead is to understand how these two checkpoints are regulated in human SLE, and to devise therapeutic strategies that target both checkpoints.

摘要

系统性红斑狼疮(SLE)是一种病因不明的慢性复杂自身免疫性疾病,其特征是存在广泛的免疫异常和多器官损伤。过去十年取得的一项重要进展是我们对不同基因位点(或基因)如何决定狼疮中特定免疫异常的理解。“基因剖析”揭示了一些笼罩狼疮发病机制的谜团。似乎至少有两个不同的事件导致疾病。第一个涉及适应性免疫系统的破坏,第二个涉及先天免疫的失调。两个检查点的协同失调是导致全面狼疮的必要条件。未来的挑战是了解这两个检查点在人类SLE中是如何调节的,并设计针对这两个检查点的治疗策略。

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