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目前治疗系统性红斑狼疮的新疗法。

Current and novel therapeutics in the treatment of systemic lupus erythematosus.

机构信息

Department of Pediatrics, Division of Pediatric Rheumatology, Morgan Stanley Children's Hospital of New York Presbyterian, Columbia University Medical Center, New York, New York, USA.

出版信息

J Allergy Clin Immunol. 2011 Feb;127(2):303-12; quiz 313-4. doi: 10.1016/j.jaci.2010.12.1087.

DOI:10.1016/j.jaci.2010.12.1087
PMID:21281862
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3053574/
Abstract

Systemic lupus erythematosus (SLE) is a complex autoimmune disease with significant clinical heterogeneity. Recent advances in our understanding of the genetic, molecular, and cellular bases of autoimmune diseases and especially SLE have led to the application of novel and targeted treatments. Although many treatment modalities are effective in lupus-prone mice, the situation is more complex in human subjects. This article reviews the general approach to the therapy of SLE, focusing on current approved therapies and novel approaches that might be used in the future.

摘要

系统性红斑狼疮(SLE)是一种复杂的自身免疫性疾病,具有显著的临床异质性。我们对自身免疫性疾病,尤其是 SLE 的遗传、分子和细胞基础的理解的最新进展,导致了新型和靶向治疗的应用。虽然许多治疗方法在狼疮易感小鼠中是有效的,但在人类受试者中情况更为复杂。本文综述了 SLE 治疗的一般方法,重点介绍了目前批准的治疗方法和未来可能使用的新方法。

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Arthritis Res Ther. 2010;12(6):R204. doi: 10.1186/ar3179. Epub 2010 Nov 4.
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TLR recognition of self nucleic acids hampers glucocorticoid activity in lupus.TLR 识别自身核酸会阻碍狼疮患者糖皮质激素的活性。
Nature. 2010 Jun 17;465(7300):937-41. doi: 10.1038/nature09102.
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Suppression of skin and kidney disease by inhibition of spleen tyrosine kinase in lupus-prone mice.
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Arthritis Res Ther. 2024 Nov 18;26(1):201. doi: 10.1186/s13075-024-03435-1.
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Implications of CD154 and Its Receptors in the Pathogenesis and Treatment of Systemic Lupus Erythematosus.CD154 及其受体在系统性红斑狼疮发病机制和治疗中的意义。
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