Sana Biotechnology, Cambridge, Massachusetts, USA.
Ultragenyx Pharmaceutical Inc, Novato, California, USA.
AAPS J. 2023 Apr 26;25(3):47. doi: 10.1208/s12248-023-00814-5.
The number of approved or investigational late phase viral vector gene therapies (GTx) has been rapidly growing. The adeno-associated virus vector (AAV) technology continues to be the most used GTx platform of choice. The presence of pre-existing anti-AAV immunity has been firmly established and is broadly viewed as a potential deterrent for successful AAV transduction with a possibility of negative impact on clinical efficacy and a connection to adverse events. Recommendations for the evaluation of humoral, including neutralizing and total antibody based, anti-AAV immune response have been presented elsewhere. This manuscript aims to cover considerations related to the assessment of anti-AAV cellular immune response, including review of correlations between humoral and cellular responses, potential value of cellular immunogenicity assessment, and commonly used analytical methodologies and parameters critical for monitoring assay performance. This manuscript was authored by a group of scientists involved in GTx development who represent several pharma and contract research organizations. It is our intent to provide recommendations and guidance to the industry sponsors, academic laboratories, and regulatory agencies working on AAV-based GTx viral vector modalities with the goal of achieving a more consistent approach to anti-AAV cellular immune response assessment.
已批准或正在研究的晚期病毒载体基因治疗(GTx)的数量正在迅速增加。腺相关病毒载体(AAV)技术仍然是最常用的 GTx 平台选择。预先存在的抗 AAV 免疫已被牢固确立,并被广泛认为是 AAV 转导成功的潜在障碍,可能对临床疗效产生负面影响,并与不良事件有关。有关评估体液免疫(包括中和和基于总抗体的免疫)的建议已在其他地方提出。本文旨在涵盖与评估抗 AAV 细胞免疫反应相关的考虑因素,包括对体液和细胞反应之间相关性的综述、细胞免疫原性评估的潜在价值,以及用于监测分析性能的常用分析方法和关键参数。本文由参与 GTx 开发的一组科学家撰写,他们代表几家制药和合同研究组织。我们的目的是为从事基于 AAV 的 GTx 病毒载体模式的行业赞助商、学术实验室和监管机构提供建议和指导,旨在实现更一致的抗 AAV 细胞免疫反应评估方法。