Skalweit Marion J
Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, OH, USA; Case Western Reserve University School of Medicine, Cleveland, OH, USA
Int J STD AIDS. 2016 Dec;27(14):1346-1349. doi: 10.1177/0956462416643852. Epub 2016 Apr 12.
Primary resistance mutations to second generation HIV non-nucleoside reverse transcriptase inhibitors are rare in HIV-infected persons in the US (estimated at 1.8%). We report an antiretroviral treatment (ART)-naïve patient with acquired immunodeficiency syndrome (AIDS) (CD4 cell count 20 cells/mm, viral load 8439 copies/mL), who was infected with HIV-1 sub-type B virus containing a reverse transcriptase mutation, E138A, associated with rilpivirine resistance. Subsequently, he was initiated on a single tablet ART regimen containing an integrase inhibitor and developed immune reconstitution inflammatory syndrome (IRIS), presenting as Mycobacterium avium cervical adenitis. The patient went on to develop rifamycin-induced neutropenia during treatment of his opportunistic infection but later recovered his counts, and remains well on an integrase-based HIV regimen. His case illustrates the growing importance of archived resistance mutations including the less common E138A mutation, as well as the risk and rapid occurrence of IRIS in AIDS patients initiated on integrase inhibitors.
在美国,HIV感染者中对第二代HIV非核苷类逆转录酶抑制剂的原发性耐药突变很少见(估计为1.8%)。我们报告了一名初治的获得性免疫缺陷综合征(AIDS)患者(CD4细胞计数为20个/mm³,病毒载量为8439拷贝/mL),他感染了含有与利匹韦林耐药相关的逆转录酶突变E138A的HIV-1 B亚型病毒。随后,他开始接受包含整合酶抑制剂的单片抗逆转录病毒治疗方案,并发生了免疫重建炎症综合征(IRIS),表现为鸟分枝杆菌颈部腺炎。该患者在治疗机会性感染期间出现了利福霉素诱导的中性粒细胞减少,但后来恢复了计数,目前在基于整合酶的HIV治疗方案下情况良好。他的病例说明了存档耐药突变(包括不太常见的E138A突变)的重要性日益增加,以及在开始使用整合酶抑制剂的AIDS患者中IRIS的风险和快速发生情况。