Department of Microbiology and Parasitology, Anhui Provincial Laboratory of Microbiology and Parasitology, Anhui Provincial Laboratory of Zoonoses of High Institutions, School of Basic Medical Sciences, Anhui Medical University, Hefei, China.
The Clinical Laboratory of the Third People's Hospital of Heifei, Hefei, China.
Parasitology. 2020 Aug;147(9):940-948. doi: 10.1017/S0031182020000177. Epub 2020 Feb 12.
The rhoptry kinase 18 of Toxoplasma gondii (TgROP18) has been identified as a key virulence factor that allows the parasite to escape from host immune defences and promotes its proliferation in host cells. Although much research is focused on the interaction between host cells and TgROP18, the development of monoclonal antibodies (mAbs) against TgROP18 has not been reported till date. To produce mAbs targeting TgROP18, two hybridomas secreting mAbs against TgROP18, designated as A1 and T2, were generated using cell fusion technology. The subtypes of the A1 and T2 mAbs were identified as IgG3 λ and IgM κ, and peptide scanning revealed that the core sequences of the antigenic epitopes were 180LRAQRRRSELVFE192 and 351NYFLLMMRAEADM363, respectively. The T2 mAb specifically reacted with both T. gondii type I and Chinese I, but not with T. gondii type II, Plasmodium falciparum or Schistosoma japonicum. Finally, the sequences of heavy chain and light chain complementarity-determining regions of T2 were amplified, cloned and characterized, making the modification of the mAb feasible in the future. The development of mAbs against TgROP18 would aid the investigation of the molecular mechanisms underlying the modulation of host cellular functions by TgROP18, and in the development of strategies to diagnose and treat Toxoplasmosis.
刚地弓形虫的 rhoptry 激酶 18(TgROP18)已被鉴定为一种关键的毒力因子,使寄生虫能够逃避宿主的免疫防御,并促进其在宿主细胞内增殖。尽管许多研究都集中在宿主细胞与 TgROP18 之间的相互作用上,但迄今为止尚未报道针对 TgROP18 的单克隆抗体(mAbs)的开发。为了产生针对 TgROP18 的 mAbs,我们使用细胞融合技术生成了两种分泌针对 TgROP18 的 mAbs 的杂交瘤,分别命名为 A1 和 T2。A1 和 T2 mAbs 的亚型被鉴定为 IgG3 λ 和 IgM κ,肽扫描显示抗原表位的核心序列分别为 180LRAQRRRSELVFE192 和 351NYFLLMMRAEADM363。T2 mAb 特异性地与刚地弓形虫 I 型和中国 I 型反应,但与刚地弓形虫 II 型、疟原虫或日本血吸虫不反应。最后,扩增、克隆和表征了 T2 的重链和轻链互补决定区序列,为未来 mAb 的修饰提供了可能。针对 TgROP18 的 mAbs 的开发将有助于研究 TgROP18 对宿主细胞功能的调节的分子机制,并有助于开发诊断和治疗弓形体病的策略。