QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
School of Medicine, University of Queensland, Brisbane, Queensland, Australia.
Science. 2019 Jan 18;363(6424):288-293. doi: 10.1126/science.aat0066.
Cytomegalovirus infection is a frequent and life-threatening complication that significantly limits positive transplantation outcomes. We developed preclinical mouse models of cytomegalovirus reactivation after transplantation and found that humoral immunity is essential for preventing viral recrudescence. Preexisting antiviral antibodies decreased after transplant in the presence of graft-versus-host disease and were not replaced, owing to poor reconstitution of donor B cells and elimination of recipient plasma cells. Viral reactivation was prevented by the transfer of immune serum, without a need to identify and target specific antigenic determinants. Notably, serotherapy afforded complete protection, provided that the serum was matched to the infecting viral strain. Thus, we define the mechanisms for cytomegalovirus reactivation after transplantation and identify a readily translatable strategy of exceptional potency, which avoids the constraints of cellular therapies.
巨细胞病毒感染是一种常见且危及生命的并发症,严重限制了移植的积极结果。我们开发了移植后巨细胞病毒再激活的临床前小鼠模型,发现体液免疫对于预防病毒复发至关重要。在移植物抗宿主病的存在下,移植后抗病毒抗体减少,并且由于供体 B 细胞的重建不良和受体浆细胞的消除,抗体没有得到替代。免疫血清的转移可以预防病毒再激活,而无需识别和靶向特定的抗原决定簇。值得注意的是,血清疗法提供了完全的保护,只要血清与感染的病毒株相匹配。因此,我们定义了移植后巨细胞病毒再激活的机制,并确定了一种具有卓越效力的易于转化的策略,该策略避免了细胞治疗的限制。