Research Institute for Children, Children's Hospital, New Orleans, Louisiana, United States of America ; Departments of Microbiology, Immunology and Parasitology, LSU Health Sciences Center, New Orleans, Louisiana, United States of America.
PLoS One. 2013 Sep 4;8(9):e73969. doi: 10.1371/journal.pone.0073969. eCollection 2013.
In humans it has been reported that a major site of the latent reservoir of HIV is within CD4+ T cells expressing the memory marker CD45RO, defined by the mAb UCHL1. There are conflicting reports regarding the expression of this antigen in macaques, the most relevant animal species for studying HIV pathogenesis and testing new therapies. There is now a major effort to eradicate HIV reservoirs and cure the infection. One approach is to eliminate subsets of cells housing the latent reservoir, using UCHL1 to target these cells. So that such studies may be performed in macaques, it is essential to determine expression of CD45RO.
We have used immunofluorescence and flow cytometry to study cell surface expression of CD45RO on lymphocytes from PBMC, lymphoid, and GI organs of rhesus, pigtailed, and cynomolgus macaques. Both direct and indirect immunofluorescence experiments were performed.
CD45RO is expressed on a subset of CD4+ lymphocytes of all pigtailed, a fraction of rhesus, and neither of the cynomolgus macaques studied. The binding of UCHL1 to macaque cells was of lower avidity than to human cells. This could be overcome by forming UCHL1 multimers. Directly conjugating fluors to UCHL1 can inhibit UCHL1 binding to macaque cells. Patterns of UCHL1 expression differ somewhat in macaques and humans, and from that of other memory markers often used in macaques.
CD45RO, defined with mAb UCHL1, is well expressed on CD4+ cells in pigtailed macaques. Using tissues recovered from latently infected pigtailed macaques we are determining whether UCHL1, or other memory markers, can define the cellular locus of the reservoir. The low avidity of this interaction could limit the utility of UCHL1, in its conventional form, to eliminate cells in vivo and test this approach in macaque models of HIV infection.
据报道,在人类中,HIV 的潜伏储存库主要位于表达记忆标志物 CD45RO 的 CD4+T 细胞中,该标志物由 mAbUCHL1 定义。关于这种抗原在猕猴中的表达存在相互矛盾的报告,猕猴是研究 HIV 发病机制和测试新疗法的最相关动物物种。现在正在努力根除 HIV 储存库并治愈感染。一种方法是使用 UCHL1 靶向这些细胞来消除储存潜伏库的细胞亚群。为了在猕猴中进行此类研究,确定 CD45RO 的表达至关重要。
我们使用免疫荧光和流式细胞术研究了来自猕猴、恒河猴和食蟹猴 PBMC、淋巴和 GI 器官的淋巴细胞表面 CD45RO 的表达。进行了直接和间接免疫荧光实验。
CD45RO 表达在所有恒河猴、部分猕猴和研究的食蟹猴的 CD4+淋巴细胞亚群上。UCHL1 与猕猴细胞的结合亲和力低于与人细胞的结合亲和力。通过形成 UCHL1 多聚体可以克服这种情况。直接将荧光团偶联到 UCHL1 上可以抑制 UCHL1 与猕猴细胞的结合。UCHL1 在猕猴和人类中的表达模式与其他在猕猴中常用的记忆标志物略有不同。
mAbUCHL1 定义的 CD45RO 在恒河猴的 CD4+细胞上表达良好。使用从潜伏感染的恒河猴中回收的组织,我们正在确定 UCHL1 或其他记忆标志物是否可以定义储存库的细胞位置。这种相互作用的低亲和力可能会限制 UCHL1 的常规形式在体内消除细胞的效用,并在猕猴 HIV 感染模型中测试这种方法。