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首页> 外文期刊>Viral immunology >Graves' disease as an immune reconstitution syndrome in an HIV-1-positive patient commencing effective antiretroviral therapy: case report and literature review.
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Graves' disease as an immune reconstitution syndrome in an HIV-1-positive patient commencing effective antiretroviral therapy: case report and literature review.

机译:在开始有效的抗逆转录病毒治疗的HIV-1阳性患者中,格雷夫斯病是免疫重建综合征:病例报告和文献复习。

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Combination antiretroviral therapy (cART) reduces morbidity and mortality in human immunodeficiency virus (HIV) infection, but it may also alter the clinical course of subclinical opportunistic infections and can even induce autoimmune disease. These atypical presentations are known as immune restoration disease (IRD), immune reconstitution syndrome/immune recovery syndrome (IRS), or immune restoration inflammatory syndrome (IRIS). We report the case of a 27-year-old, HIV-1-positive woman who developed hyperthyroidism attributable to Graves' disease (GD) after commencing potent cART. At the initiation of cART, her CD4 T cell count was 15 cells/microL and plasma HIV RNA 35 000 copies/mL. Her commencement of cART resulted in complete viral suppression and subsequent improvement of the CD4 T-cell count. Three years later, the diagnosis of GD was established based on a typical clinical picture and the results of hormonal and immunological analyses. It coincided with a 58-fold rise of the CD4 T cells. Retrospective analysis of serum samples revealed normal thyroid function and lack of anti-thyroid peroxidase (anti-TPO), anti- thyroid-stimulating hormone receptor (anti-TSHR), and anti-thyroglobulin (anti-TG) autoantibodies at the beginning of cART. HLA class II gene examination did not reveal susceptibility for the GD development in this patient. We suggest that GD in our patient was an IRD, and advise this as a possible differential diagnosis in patients presenting with hyperthyroidism on cART. To provide further details relevant to this case, we also review the literature concerning IRD-GD.
机译:联合抗逆转录病毒疗法(cART)可以降低人类免疫缺陷病毒(HIV)感染的发病率和死亡率,但它也可能改变亚临床机会性感染的临床过程,甚至可以诱发自身免疫性疾病。这些非典型表现被称为免疫恢复疾病(IRD),免疫重建综合征/免疫恢复综合征(IRS)或免疫恢复炎症综合征(IRIS)。我们报告一例27岁的HIV-1阳性妇女,在开始有效的cART治疗后发展为可归因于Graves病(GD)的甲状腺功能亢进症。在开始cART时,她的CD4 T细胞计数为15细胞/微升,血浆HIV RNA为35000拷贝/毫升。她开始使用cART可以完全抑制病毒并随后改善CD4 T细胞计数。三年后,根据典型的临床表现以及激素和免疫学分析结果确定了GD的诊断。它与CD4 T细胞的58倍上升同时发生。血清样本的回顾性分析显示,在开始cART时,甲状腺功能正常,缺乏抗甲状腺过氧化物酶(anti-TPO),抗甲状腺刺激激素受体(anti-TSHR)和抗甲状腺球蛋白(anti-TG)自身抗体。 。 HLA II类基因检查未显示该患者发生GD的敏感性。我们建议患者中的GD为IRD,建议将其作为cART甲亢患者的可能的鉴别诊断。为了提供与该案例有关的更多详细信息,我们还回顾了有关IRD-GD的文献。

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