Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA, USA.
Division of HIV, Infectious Diseases and Global Medicine, University of California San Francisco, San Francisco, CA, USA.
Nat Commun. 2022 Mar 9;13(1):1219. doi: 10.1038/s41467-022-28727-5.
A major obstacle to achieving long-term antiretroviral (ART) free remission or functional cure of HIV infection is the presence of persistently infected cells that establish a long-lived viral reservoir. HIV largely resides in anatomical regions that are inaccessible to routine sampling, however, and non-invasive methods to understand the longitudinal tissue-wide burden of HIV persistence are urgently needed. Positron emission tomography (PET) imaging is a promising strategy to identify and characterize the tissue-wide burden of HIV. Here, we assess the efficacy of using immunoPET imaging to characterize HIV reservoirs and identify anatomical foci of persistent viral transcriptional activity using a radiolabeled HIV Env-specific broadly neutralizing antibody, Zr-VRC01, in HIV-infected individuals with detectable viremia and on suppressive ART compared to uninfected controls (NCT03729752). We also assess the relationship between PET tracer uptake in tissues and timing of ART initiation and direct HIV protein expression in CD4 T cells obtained from lymph node biopsies. We observe significant increases in Zr-VRC01 uptake in various tissues (including lymph nodes and gut) in HIV-infected individuals with detectable viremia (N = 5) and on suppressive ART (N = 5) compared to uninfected controls (N = 5). Importantly, PET tracer uptake in inguinal lymph nodes in viremic and ART-suppressed participants significantly and positively correlates with HIV protein expression measured directly in tissue. Our strategy may allow non-invasive longitudinal characterization of residual HIV infection and lays the framework for the development of immunoPET imaging in a variety of other infectious diseases.
实现长期抗逆转录病毒(ART)缓解或功能性治愈 HIV 感染的主要障碍是存在持续感染的细胞,这些细胞建立了一个长期存在的病毒储存库。然而,HIV 主要存在于常规采样无法到达的解剖区域,因此迫切需要非侵入性方法来了解 HIV 持续存在的纵向组织负担。正电子发射断层扫描(PET)成像技术是一种有前途的策略,可以识别和描述 HIV 储存库,并使用放射性标记的 HIV Env 特异性广泛中和抗体 Zr-VRC01 来表征组织范围内的 HIV 持续转录活性,该抗体可用于 HIV 感染个体,这些个体的病毒载量可检测到且正在接受抑制性 ART,与未感染对照者(NCT03729752)相比。我们还评估了 PET 示踪剂在组织中的摄取与 ART 起始时间以及从淋巴结活检中获得的 CD4 T 细胞中直接 HIV 蛋白表达之间的关系。我们观察到,与未感染对照者(N = 5)相比,在可检测到病毒载量的 HIV 感染个体(N = 5)和接受抑制性 ART 的个体(N = 5)中,各种组织(包括淋巴结和肠道)中 Zr-VRC01 的摄取显著增加。重要的是,在病毒载量可检测和 ART 抑制的参与者的腹股沟淋巴结中,PET 示踪剂摄取与直接在组织中测量的 HIV 蛋白表达呈显著正相关。我们的策略可能允许对残留 HIV 感染进行非侵入性的纵向描述,并为在各种其他传染病中开发免疫 PET 成像奠定了框架。