Onnockx Sheela, Baldo Aline, Pauwels Katia
Sciensano, Service Biosafety and Biotechnology, Rue Juliette Wytsmanstraat 14, B-1050 Brussels, Belgium.
Vaccines (Basel). 2023 Sep 1;11(9):1448. doi: 10.3390/vaccines11091448.
Attenuated and/or genetically modified oncolytic viruses (OV) gain increasing interest as a promising approach for cancer therapy. Beside the assessment of subject safety, quality and efficacy aspects of medicinal products for human use, genetically modified viruses are also governed by EU regulatory frameworks requiring an environmental risk assessment (ERA). An important element to be assessed as part of the ERA is the incidence of exposure to OV of individuals, other than the trial subjects, and the environment. The evidence-based evaluation of shedding data is considered to be decisive in that context, as it may impact the OV capacity to be transmitted. This is particularly true for OV still able to (conditionally) replicate as opposed to replication-defective viral vectors commonly used in gene therapy or vaccination. To our knowledge, this article presents the most extensive and up-to-date review of shedding data reported with OV employed in clinics. Besides the identification of a topical need for improving the collection of shedding data, this article aims at providing an aid to the design of an appropriate shedding study, thereby relying on and further complementing principles described in existing guidelines issued by European and international institutions.
减毒和/或基因改造的溶瘤病毒(OV)作为一种有前景的癌症治疗方法,越来越受到关注。除了评估人用药品的安全性、质量和有效性外,基因改造病毒还受欧盟监管框架的约束,需要进行环境风险评估(ERA)。作为ERA评估的一个重要因素,是除试验对象外的个体和环境接触OV的发生率。在这种情况下,基于证据对脱落数据的评估被认为是决定性的,因为它可能影响OV的传播能力。对于仍能(有条件地)复制的OV来说尤其如此,这与基因治疗或疫苗接种中常用的复制缺陷病毒载体不同。据我们所知,本文对临床使用的OV报告的脱落数据进行了最广泛和最新的综述。除了确定改进脱落数据收集的局部需求外,本文旨在为设计适当的脱落研究提供帮助,从而依赖并进一步补充欧洲和国际机构发布的现有指南中描述的原则。