Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, 1855 W Taylor Street, M/C 648, Chicago, IL 60612, USA.
Graefes Arch Clin Exp Ophthalmol. 2010 May;248(5):737-40. doi: 10.1007/s00417-009-1283-3. Epub 2010 Jan 22.
We report a case of recurrent cytomegalovirus (CMV) retinitis in an HIV-negative patient with CD4+ T lymphocytopenia.
Case report.
A 41-year-old HIV-negative woman with a history of systemic lupus erythematosus, idiopathic thrombocytopenic purpura requiring splenectomy, and diabetes presented with primary CMV infection, high-grade viremia, CMV pneumonia followed by CMV retinitis (CMVR) and a CD4+ T lymphocyte (CD4) count of 12 cells/mm(3) after therapy with rituximab, prednisone, and methotrexate. Persistent CMV viremia led to genotypic analysis of the circulating virus, which revealed UL97 and UL54 mutations known to be associated with resistance to ganciclovir (GCV) and cidofovir. CMV clearance from the bloodstream followed systemic antiviral therapy and recovery of CD4 cell count. However, CMVR recurred multiple times despite GCV implants, systemic valganciclovir, intravitreal GCV injections, and persistent CD4 counts greater than 100 cells/mm(3). Recurrent episodes of CMVR responded to multiple high dose intravitreal GCV injections (5000-6000 micrograms) and recovery of CD4 cell counts to greater than 200 cells/mm(3).
This case demonstrates that recurrent CMVR occurs in HIV-negative patients at CD4 cell counts thought to be protective in HIV patients, and suggests that an ineffective local immune response to retinal infection combined with CMV drug resistance may have been important factors leading to recurrent disease in this patient. Treatment producing high local concentrations of GCV may be effective therapy for CMV retinitis due to GCV-resistant virus.
我们报告了一例 HIV 阴性患者出现复发性巨细胞病毒(CMV)视网膜炎,该患者存在 CD4+T 淋巴细胞减少症。
病例报告。
一名 41 岁 HIV 阴性女性,患有系统性红斑狼疮、特发性血小板减少性紫癜(需行脾切除术)和糖尿病,因原发性 CMV 感染、高病毒载量血症、CMV 性肺炎继发 CMV 视网膜炎以及利妥昔单抗、泼尼松和甲氨蝶呤治疗后 CD4+T 淋巴细胞(CD4)计数 12 个/mm³而就诊。持续性 CMV 病毒血症导致循环病毒的基因分型分析,结果显示 UL97 和 UL54 突变,已知这些突变与更昔洛韦(GCV)和西多福韦耐药相关。在全身抗病毒治疗和 CD4 细胞计数恢复后,CMV 从血液中清除。然而,尽管给予 GCV 植入物、全身缬更昔洛韦、玻璃体内 GCV 注射以及 CD4 计数持续大于 100 个/mm³,CMVR 仍多次复发。多次复发性 CMVR 对多次高剂量玻璃体内 GCV 注射(5000-6000 微克)和 CD4 细胞计数恢复至大于 200 个/mm³有反应。
该病例表明,在 CD4 细胞计数被认为对 HIV 患者具有保护作用的 HIV 阴性患者中,会出现复发性 CMVR,并且提示针对视网膜感染的局部免疫反应无效和 CMV 耐药可能是导致该患者疾病复发的重要因素。产生高局部 GCV 浓度的治疗可能是治疗 GCV 耐药性 CMV 视网膜炎的有效方法。