“当HIV与MG相遇时:是否存在免疫重建?”

Aditya Vijayakrishnan Nair, Lesley Ponraj, Ajith Sivadasan, Sanjit Aaron
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引用次数: 0

摘要

自身免疫性疾病和人类免疫缺陷病毒(HIV)阳性很少共存。我们报告一例抗肌肉特异性激酶(MuSK)抗体阳性的重症肌无力(MuSK+ MG)在HIV阳性患者。抗逆转录病毒治疗导致免疫重建综合征,导致MG症状恶化。然而,在这种情况下,额外的免疫调节的作用尚未得到澄清。病例表现:一名44岁女性,病毒学抑制HIV感染,表现为波动性眼球症状、肢体无力和呼吸衰竭。这些症状在抗逆转录病毒治疗(ART)修改后约6个月被注意到。电生理研究和抗MuSK抗体水平升高证实了MuSK + MG。在ART修饰后,CD4细胞计数从115个增加到681个/µL,这与免疫重建是一致的。皮质类固醇、利妥昔单抗和机会性感染预防治疗使她的MG症状减轻,无不良副作用。结论:本病例强调了管理HIV自身免疫性疾病的复杂性,art诱导的免疫重建可能揭示或触发自身免疫。早期诊断和靶向治疗可以改善预后。在这种情况下,利妥昔单抗开始促进症状控制和类固醇逐渐减少。需要一个多学科的方法来平衡免疫抑制和感染风险已被强调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
“When HIV meets MG: Is immune reconstitution in the mix?”

Background

Autoimmune disorders and human immunodeficiency virus (HIV) positivity rarely coexist. We report a case of anti-muscle-specific kinase (MuSK) antibody-positive myasthenia gravis (MuSK+ MG) in an HIV positive patient. Antiretroviral therapy resulted in an immune reconstitution syndrome, resulting in worsening of MG symptoms. However, the role of additional immunomodulation in this setting has yet to be clarified.

Case Presentation

A 44-year-old woman with virologically suppressed HIV infection presented with fluctuating oculobulbar symptoms, limb weakness, and respiratory failure. These symptoms were noticed around 6 months following antiretroviral therapy (ART) modification. Electrophysiological studies and elevated anti-MuSK antibody levels confirmed MuSK + MG. An increase in the CD4 count from 115 to 681 cells/µL following the ART modification was consistent with immune reconstitution. Treatment with corticosteroids, Rituximab, and opportunistic infection prophylaxis resulted in a reduction in her MG symptoms with no adverse side effects.

Conclusions

This case underscores the complexities of managing autoimmune diseases in HIV, where ART-induced immune reconstitution may unmask or trigger autoimmunity. Early diagnosis and targeted therapies can improve outcomes. In this case, Rituximab initiation facilitated symptom control and steroid tapering. The need for a multidisciplinary approach to balance immunosuppression and infection risks has been emphasized.
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