Heckmann Jeannine M, Marais Suzaan
Neurology, Department of Medicine, Groote Schuur Hospital and University of Cape Town, Cape Town, South Africa.
Neurology Research Group, UCT Neuroscience Institute, University of Cape Town, Cape Town, South Africa.
Front Neurol. 2020 Aug 21;11:775. doi: 10.3389/fneur.2020.00775. eCollection 2020.
South Africa is home to more than seven million people living with human immunodeficiency virus (HIV) and a high prevalence of tuberculosis. Human immunodeficiency virus-infected individuals may develop myasthenia gravis (MG), which raises questions regarding their management. An MG database, with 24 years of observational data, was audited for HIV-infected persons. Case reports of MG in HIV-infected persons were reviewed. We identified 17 persons with MG and HIV infection. All had generalized MG with a mean age at onset of 37.8 years. Eleven had acetylcholine receptor antibody-positive MG; one had antibodies against muscle-specific kinase. Six developed MG prior to HIV infection (mean CD4 361 cells/mm); four worsened <6 months of starting antiretrovirals. Eleven developed MG while HIV-infected (mean CD4 423 cells/mm); five presented with mild MG; three in MG crisis requiring rescue therapies (intravenous immune globulin or plasma exchange and/or intravenous cyclophosphamide). Two were diagnosed with HIV infection and MG at the same time. Fifteen required maintenance steroid-sparing immune therapies, predominantly azathioprine, or methotrexate. Plasma HIV viral loads remained below detectable levels on antiretrovirals during immunosuppressant treatment. Over the average follow-up of 6 years, 10 achieved minimal manifestation status, and the remainder improved to mild symptoms. Three cases had tuberculosis before MG, but none developed tuberculosis reactivation on immunosuppressive therapy; one used isoniazid prophylaxis. Herpes zoster reactivation during treatment occurred in one. Conclusions include the following: MG in HIV-infected patients should be managed similarly to individuals without HIV infection; half develop moderate-severe MG; MG symptoms may worsen within 6 months of antiretroviral initiation; safety monitoring must include plasma HIV viral load estimation. Isoniazid prophylaxis may not be indicated in all cases.
南非有超过700万人感染了人类免疫缺陷病毒(HIV),结核病患病率也很高。感染人类免疫缺陷病毒的个体可能会患上重症肌无力(MG),这引发了关于其治疗的问题。我们对一个拥有24年观察数据的MG数据库中感染HIV的患者进行了审核。对HIV感染者中MG的病例报告进行了回顾。我们确定了17例MG合并HIV感染的患者。所有患者均为全身型MG,发病时的平均年龄为37.8岁。11例为乙酰胆碱受体抗体阳性MG;1例有针对肌肉特异性激酶的抗体。6例在HIV感染之前患上MG(平均CD4为361个细胞/mm³);4例在开始抗逆转录病毒治疗后不到6个月病情恶化。11例在感染HIV期间患上MG(平均CD4为423个细胞/mm³);5例表现为轻度MG;3例处于MG危象,需要抢救治疗(静脉注射免疫球蛋白或血浆置换和/或静脉注射环磷酰胺)。2例同时被诊断为HIV感染和MG。15例需要维持使用减少类固醇的免疫疗法,主要是硫唑嘌呤或甲氨蝶呤。在免疫抑制治疗期间,抗逆转录病毒药物治疗下血浆HIV病毒载量仍低于可检测水平。在平均6年的随访中,10例达到最小表现状态,其余患者症状改善为轻度。3例在MG之前患有结核病,但在免疫抑制治疗期间均未发生结核病复发;1例使用异烟肼进行预防。治疗期间有1例发生带状疱疹再激活。结论如下:HIV感染患者的MG治疗应与未感染HIV的个体类似;一半患者发展为中重度MG;MG症状可能在开始抗逆转录病毒治疗后6个月内恶化;安全监测必须包括血浆HIV病毒载量评估。并非所有病例都需要使用异烟肼进行预防。