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抗拓扑异构酶 I 抗体和抗着丝点抗体在系统性硬化症患者中的共存。利妥昔单抗联合尼达尼布治疗的疗效。病例报告。

Coexistence of anti-topoisomerase I and anticentromere antibodies in a patient with systemic sclerosis. Efficacy of treatment combining rituximab and nintedanib. A case report.

机构信息

Department of Rheumatology, 16804Doctor Peset University Hospital, Valencia, Spain.

Autoimmunity Laboratory, 16804Doctor Peset University Hospital, Valencia, Spain.

出版信息

Int J Immunopathol Pharmacol. 2022 Jan-Dec;36:3946320221115310. doi: 10.1177/03946320221115310.

Abstract

In the diagnostic of systemic sclerosis (SSc), both anti-centromere (ACA) and anti-topoisomerase I (ATA) antibodies are considered mutually exclusive, though their coexistence has been also reported in some patients. Notably, nintedanib has been approved for the treatment of interstitial lung disease associated to SSc. Herein, we present the clinical case of a 41-year-old woman with SSc who shows an immunological seroconversion (from ACA positivity to a coexistence of ACA and ATA antibodies) together with changes in her clinical phenotype. Besides, the patient responds positively to the treatment of her lung involvement with a combination of immunomodulators and antifibrotic agents.

摘要

在系统性硬化症(SSc)的诊断中,抗着丝点(ACA)和抗拓扑异构酶 I(ATA)抗体被认为是相互排斥的,尽管在一些患者中也有报道它们同时存在。值得注意的是,尼达尼布已被批准用于治疗与 SSc 相关的间质性肺疾病。在此,我们报告了一例 41 岁女性 SSc 患者的临床病例,该患者表现出免疫血清学转换(从 ACA 阳性转为 ACA 和 ATA 抗体共存),同时其临床表型也发生了变化。此外,患者对免疫调节剂和抗纤维化药物联合治疗其肺部受累反应良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6556/9393658/25f530d0834d/10.1177_03946320221115310-fig1.jpg

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