Institute of Bioengineering, ChongQing Academy of Animal Sciences, Chongqing, China.
Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Front Immunol. 2022 Sep 23;13:992787. doi: 10.3389/fimmu.2022.992787. eCollection 2022.
The coronavirus disease 2019 pandemic has caused more than 532 million infections and 6.3 million deaths to date. The reactive and neutralizing fully human antibodies of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are effective detection tools and therapeutic measures. During SARS-CoV-2 infection, a large number of SARS-CoV-2 reactive and neutralizing antibodies will be produced. Most SARS-CoV-2 reactive and neutralizing fully human antibodies are isolated from human and frequently encoded by convergent heavy-chain variable genes. However, SARS-CoV-2 viruses can mutate rapidly during replication and the resistant variants of neutralizing antibodies easily survive and evade the immune response, especially in the face of such focused antibody responses in humans. Therefore, additional tools are needed to develop different kinds of fully human antibodies to compensate for current deficiency. In this study, we utilized antibody humanized CAMouse mice to develop a rapid antibody discovery method and examine the antibody repertoire of SARS-CoV-2 RBD-reactive hybridoma cells derived from CAMouse mice by using high-throughput single-cell V(D)J sequencing analysis. CAMouse mice were immunized by 28-day rapid immunization method. After electrofusion and semi-solid medium screening on day 12 post-electrofusion, 171 hybridoma clones were generated based on the results of SARS-CoV-2 RBD binding activity assay. A rather obvious preferential usage of IGHV6-1 family was found in these hybridoma clones derived from CAMouse mice, which was significantly different from the antibodies found in patients with COVID-19. After further virus neutralization screening and antibody competition assays, we generated a noncompeting two-antibody cocktail, which showed a potent prophylactic protective efficacy against SARS-CoV-2 in cynomolgus macaques. These results indicate that humanized CAMouse mice not only provide a valuable platform to obtain fully human reactive and neutralizing antibodies but also have a different antibody repertoire from humans. Thus, humanized CAMouse mice can be used as a good complementary tool in discovery of fully human therapeutic and diagnostic antibodies.
新型冠状病毒病 2019 大流行迄今已导致超过 5.32 亿感染和 630 万人死亡。严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的反应性和中和性全人源抗体是有效的检测工具和治疗措施。在 SARS-CoV-2 感染期间,会产生大量的 SARS-CoV-2 反应性和中和性抗体。大多数 SARS-CoV-2 反应性和中和性全人源抗体是从人类中分离出来的,并且经常由会聚的重链可变基因编码。然而,SARS-CoV-2 病毒在复制过程中会迅速发生突变,中和抗体的耐药变体很容易存活并逃避免疫反应,尤其是在人类面临这种集中的抗体反应时。因此,需要开发额外的工具来开发不同类型的全人源抗体以弥补当前的不足。在这项研究中,我们利用抗体人源化 CAMouse 小鼠开发了一种快速抗体发现方法,并通过高通量单细胞 V(D)J 测序分析来检查源自 CAMouse 小鼠的 SARS-CoV-2 RBD 反应性杂交瘤细胞的抗体库。CAMouse 小鼠通过 28 天快速免疫方法进行免疫。电融合后 12 天,基于 SARS-CoV-2 RBD 结合活性测定的结果,通过电融合和半固体培养基筛选,共生成 171 个杂交瘤克隆。从 CAMouse 小鼠衍生的杂交瘤克隆中发现了明显的 IGHV6-1 家族的优先使用,这与 COVID-19 患者中的抗体明显不同。经过进一步的病毒中和筛选和抗体竞争实验,我们生成了一种非竞争的双抗体鸡尾酒,该鸡尾酒在食蟹猴中对 SARS-CoV-2 显示出强大的预防保护作用。这些结果表明,人源化 CAMouse 小鼠不仅提供了获得全人源反应性和中和性抗体的有价值的平台,而且具有与人类不同的抗体库。因此,人源化 CAMouse 小鼠可用作发现全人源治疗性和诊断性抗体的良好补充工具。