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AAV 长效递送抗 SIV 单克隆抗体。

Long-Term Delivery of an Anti-SIV Monoclonal Antibody With AAV.

机构信息

Department of Pathology, Miller School of Medicine, University of Miami, Miami, FL, United States.

Wisconsin National Primate Research Center, University of Wisconsin, Madison, WI, United States.

出版信息

Front Immunol. 2020 Mar 17;11:449. doi: 10.3389/fimmu.2020.00449. eCollection 2020.

Abstract

Long-term delivery of anti-HIV monoclonal antibodies using adeno-associated virus (AAV) holds promise for the prevention and treatment of HIV infection. We previously reported that after receiving a single administration of AAV vector coding for anti-SIV antibody 5L7, monkey 84-05 achieved high levels of AAV-delivered 5L7 IgG1 which conferred sterile protection against six successive, escalating dose, intravenous challenges with highly infectious, highly pathogenic SIVmac239, including a final challenge with 10 animal infectious doses (1). Here we report that monkey 84-05 has successfully maintained 240-350 μg/ml of anti-SIV antibody 5L7 for over 6 years. Approximately 2% of the circulating IgG in this monkey is this one monoclonal antibody. This monkey generated little or no anti-drug antibodies (ADA) to the AAV-delivered antibody for the duration of the study. Due to the nature of the high-dose challenge used and in order to rule out a potential low-level infection not detected by regular viral loads, we have used ultrasensitive techniques to detect cell-associated viral DNA and RNA in PBMCs from this animal. In addition, we have tested serum from 84-05 by ELISA against overlapping peptides spanning the whole envelope sequence for SIVmac239 (PepScan) and against recombinant p27 and gp41 proteins. No reactivity has been detected in the ELISAs indicating the absence of naturally arising anti-SIV antibodies; moreover, the ultrasensitive cell-associated viral tests yielded no positive reaction. We conclude that macaque 84-05 was effectively protected and remained uninfected. Our data show that durable, continuous antibody expression can be achieved after one single administration of AAV and support the potential for lifelong protection against HIV from a single vector administration.

摘要

使用腺相关病毒(AAV)长期递送抗 HIV 单克隆抗体有望预防和治疗 HIV 感染。我们之前报道过,在接受单次给予编码抗 SIV 抗体 5L7 的 AAV 载体后,猴子 84-05 实现了高水平的 AAV 递送 5L7 IgG1,从而对六次连续递增剂量的具有高度传染性和高致病性的 SIVmac239 静脉内挑战提供了无菌保护,包括最后一次用 10 个动物感染剂量(1)进行挑战。在这里,我们报告说猴子 84-05 已经成功地将抗 SIV 抗体 5L7 的水平维持在 240-350μg/ml 超过 6 年。在这只猴子的循环 IgG 中,大约有 2%是这种单克隆抗体。在研究期间,这只猴子对 AAV 递送的抗体几乎没有或没有产生抗药物抗体(ADA)。由于使用了高剂量挑战的性质,并为了排除常规病毒载量未检测到的潜在低水平感染,我们使用超灵敏技术检测了来自该动物的 PBMC 中的细胞相关病毒 DNA 和 RNA。此外,我们通过 ELISA 用针对 SIVmac239 包膜序列全长的重叠肽(PepScan)和针对重组 p27 和 gp41 蛋白对 84-05 的血清进行了检测。ELISAs 未检测到反应性,表明不存在自然产生的抗 SIV 抗体;此外,超灵敏的细胞相关病毒检测未产生阳性反应。我们得出结论,食蟹猴 84-05 得到了有效保护,并且未被感染。我们的数据表明,单次给予 AAV 后可以实现持久的、连续的抗体表达,并支持单次载体给药可实现对 HIV 的终身保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb62/7089924/5baffa3aa334/fimmu-11-00449-g0001.jpg

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