Sigmovir Biosystems, Inc., Rockville, Maryland, United States of America.
University of Massachusetts Chan Medical School, Worcester, Massachusetts United States of America.
PLoS Pathog. 2021 Dec 23;17(12):e1009856. doi: 10.1371/journal.ppat.1009856. eCollection 2021 Dec.
Maternal anti-respiratory syncytial virus (RSV) antibodies acquired by the fetus through the placenta protect neonates from RSV disease through the first weeks of life. In the cotton rat model of RSV infections, we previously reported that immunization of dams during pregnancy with virus-like particles assembled with mutation stabilized pre-fusion F protein as well as the wild type G protein resulted in robust protection of their offspring from RSV challenge. Here we describe the durability of those protective responses in dams, the durability of protection in offspring, and the transfer of that protection to offspring of two consecutive pregnancies without a second boost immunization. We report that four weeks after birth, offspring of the first pregnancy were significantly protected from RSV replication in both lungs and nasal tissues after RSV challenge, but protection was reduced in pups at 6 weeks after birth. However, the overall protection of offspring of the second pregnancy was considerably reduced, even at four weeks of age. This drop in protection occurred even though the levels of total anti-pre-F IgG and neutralizing antibody titers in dams remained at similar, high levels before and after the second pregnancy. The results are consistent with an evolution of antibody properties in dams to populations less efficiently transferred to offspring or the less efficient transfer of antibodies in elderly dams.
母体抗呼吸道合胞病毒(RSV)抗体通过胎盘传递给胎儿,可在生命的头几周保护新生儿免受 RSV 疾病的侵害。在 RSV 感染的棉鼠模型中,我们之前报道称,在妊娠期间用突变稳定的预融合 F 蛋白和野生型 G 蛋白组装而成的病毒样颗粒对母体进行免疫接种,可使后代对 RSV 攻击产生强大的保护作用。在这里,我们描述了母体中这些保护反应的持久性、后代的保护持久性以及无需第二次加强免疫即可将这种保护作用传递给连续两次妊娠的后代的情况。我们报告称,在 RSV 攻击后,第一次妊娠的后代在出生后四周时,肺部和鼻组织中的 RSV 复制明显受到保护,但在出生后 6 周时,幼崽的保护作用减弱。然而,第二次妊娠后代的整体保护作用明显降低,即使在 4 周龄时也是如此。即使在第二次妊娠前后,母体内总抗前 F IgG 和中和抗体滴度仍保持在相似的高水平,这种保护作用的下降仍然存在。这些结果与母体抗体特性的进化相一致,即向后代传递的效率降低或老年母体中抗体的传递效率降低。