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不同预融合F VLP免疫的棉鼠母鼠及其后代抗体群体的比较。

Comparisons of Antibody Populations in Different Pre-Fusion F VLP-Immunized Cotton Rat Dams and Their Offspring.

作者信息

Cullen Lori M, Boukhvalova Marina S, Blanco Jorge C G, Morrison Trudy G

机构信息

Department of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, MA 01655, USA.

Sigmovir Biosystems Inc., Rockville, MD 20850, USA.

出版信息

Vaccines (Basel). 2020 Mar 18;8(1):133. doi: 10.3390/vaccines8010133.

Abstract

Respiratory syncytial virus (RSV) infection poses a significant risk for infants. Since the direct vaccination of infants is problematic, maternal vaccination may provide a safer, more effective approach to their protection. In the cotton rat (CR) model, we have compared the immunization of pregnant CR dams with virus-like particles assembled with the prototype mutation stabilized pre-fusion F protein, DS-Cav1, as well two alternative mutation stabilized pre-fusion proteins (UC-2 F, UC-3 F) and showed that the alternative pre-fusion F VLPs protected the offspring of immunized dams significantly better than DS-Cav1 F VLPs (Blanco, et al. J. Virol. 93: e00914). Here, we have addressed the reasons for this increased protection by characterizing the specificities of antibodies in the sera of both immunized dams and their offspring. The approach was to measure the levels of total anti-pre-F IgG serum antibodies that would block the binding of representative pre-fusion specific monoclonal antibodies to soluble pre-fusion F protein targets. Strikingly, we found that the sera in most offspring of DS-Cav1 F VLP-immunized dams had no mAb D25-blocking antibodies, although their dams had robust levels. In contrast, all offspring of UC-3 F VLP-immunized dams had robust levels of these D25-blocking antibodies. Both sets of pup sera had significant levels of mAb AM14-blocking antibodies, indicating that all pups received maternal antibodies. A lack of mAb D25-blocking antibodies in the offspring of DS-Cav1 F VLP-immunized dams may account for the lower protection of their pups from challenge compared to the offspring of UC-3 F VLP-immunized dams.

摘要

呼吸道合胞病毒(RSV)感染对婴儿构成重大风险。由于直接给婴儿接种疫苗存在问题,母体接种疫苗可能为保护婴儿提供一种更安全、更有效的方法。在棉鼠(CR)模型中,我们比较了用原型突变稳定化前融合F蛋白DS-Cav1组装的病毒样颗粒对怀孕的CR母鼠进行免疫,以及用另外两种突变稳定化前融合蛋白(UC-2 F、UC-3 F)进行免疫的效果,结果表明,与DS-Cav1 F病毒样颗粒相比,替代前融合F病毒样颗粒能更好地保护免疫母鼠的后代(布兰科等人,《病毒学杂志》93:e00914)。在此,我们通过表征免疫母鼠及其后代血清中抗体的特异性,探讨了这种增强保护作用的原因。方法是测量总抗前F IgG血清抗体水平,这些抗体可阻断代表性的前融合特异性单克隆抗体与可溶性前融合F蛋白靶点的结合。令人惊讶的是,我们发现,尽管DS-Cav1 F病毒样颗粒免疫母鼠的血清中有大量的抗体,但大多数其后代的血清中却没有能阻断单克隆抗体D25的抗体。相比之下,UC-3 F病毒样颗粒免疫母鼠的所有后代都有大量的这种能阻断D25的抗体。两组幼鼠血清中都有大量能阻断单克隆抗体AM14的抗体,这表明所有幼鼠都获得了母体抗体。与UC-3 F病毒样颗粒免疫母鼠的后代相比,DS-Cav1 F病毒样颗粒免疫母鼠的后代缺乏能阻断单克隆抗体D25的抗体,这可能是其幼鼠受到攻击时保护作用较低的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a95/7157610/06a237f1bc6b/vaccines-08-00133-g0A1.jpg

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