Department of Pathobiology, University of Guelph, Guelph, Ontario, Canada.
Special Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
J Infect Dis. 2023 Nov 13;228(Suppl 7):S682-S690. doi: 10.1093/infdis/jiad345.
Although there are no approved countermeasures available to prevent or treat disease caused by Marburg virus (MARV), potently neutralizing monoclonal antibodies (mAbs) derived from B cells of human survivors have been identified. One such mAb, MR191, has been shown to provide complete protection against MARV in nonhuman primates. We previously demonstrated that prophylactic administration of an adeno-associated virus (AAV) expressing MR191 protected mice from MARV. Here, we modified the AAV-MR191 coding sequence to enhance efficacy and reevaluated protection in a guinea pig model. Remarkably, 4 different variants of AAV-MR191 provided complete protection against MARV, despite administration 90 days prior to challenge. Based on superior expression kinetics, AAV-MR191-io2, was selected for evaluation in a dose-reduction experiment. The highest dose provided 100% protection, while a lower dose provided ∼88% protection. These data confirm the efficacy of AAV-mediated expression of MR191 and support the further development of this promising MARV countermeasure.
虽然目前尚无批准的对策可用于预防或治疗马尔堡病毒(MARV)引起的疾病,但已从人类幸存者的 B 细胞中鉴定出具有强大中和作用的单克隆抗体(mAbs)。其中一种 mAb,MR191,已被证明可在非人类灵长类动物中提供针对 MARV 的完全保护。我们之前证明,预防性给予表达 MR191 的腺相关病毒(AAV)可保护小鼠免受 MARV 的侵害。在这里,我们修改了 AAV-MR191 的编码序列以提高功效,并在豚鼠模型中重新评估了保护作用。值得注意的是,尽管在挑战前 90 天给予了 4 种不同的 AAV-MR191 变体,但仍能提供针对 MARV 的完全保护。基于优越的表达动力学,选择 AAV-MR191-io2 进行剂量降低实验的评估。最高剂量可提供 100%的保护,而较低剂量可提供约 88%的保护。这些数据证实了 AAV 介导的 MR191 表达的功效,并支持进一步开发这种有前途的 MARV 对策。