Preparation, Purification and Performance Evaluation of Polyclonal Antibody Against SARS-CoV-2 Produced in Rat.

IF 3.1 Q2 PHARMACOLOGY & PHARMACY
Fatemeh Yaghoobizadeh, Mohammad Roayaei Ardakani, Mohammad Mehdi Ranjbar, Mohammad Khosravi, Hamid Galehdari
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Abstract

Purpose: Among all known human coronaviruses, some viruses (e.g., SARS-CoV-2) cause severe pneumonia or even death. With the regard to its spread and the importance of its rapid identification/treatment, and because pAbs are relatively cheap, able to bind to more sites on antigens and even neutralize them, this study was done for the production and purification of anti-SARS-CoV-2 polyclonal antibodies (pAb) in rats.

Methods: Viral antigen purification was performed by PEG/NaCl precipitation. The efficiency of the sucrose cushion method was also investigated to produce a purer antigen. Immunization was done and antibody purification was performed by ammonium sulfate precipitation (33%), dialysis, and ion-exchange chromatography. Western blotting and enzyme-linked immunosorbent assay (ELISA) were performed to verify the antibody specificity. All data were analyzed by SPSS software.

Results: The results showed that the amount of concentrated virus increased with the increase of PEG concentration. Moreover, the sucrose cushion method increased its purity. Besides, induction of immune response in rats for pAb production with high titers was reached via these antigens and ELISA/western blot results indicated a suitable antibody-antigen interaction. Additionally, it was shown that ion-exchange chromatography could be a suitable technique for IgG purification.

Conclusion: Herein, we presented a simple and cheap method for the purification of whole viral particles with relatively high quality. The results verified that these antigens could elicit a good immune response in the rat. The obtained pAbs showed a good specificity toward SARS-CoV-2 antigens. Accordingly, this study proposes a promising method for viral vaccine development.

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大鼠抗SARS-CoV-2多克隆抗体的制备、纯化及性能评价
目的:在所有已知的人类冠状病毒中,有些病毒(如SARS-CoV-2)会导致严重的肺炎甚至死亡。考虑到其广泛性和快速识别/治疗的重要性,并且由于pAb相对便宜,能够结合抗原上的更多位点甚至中和抗原,本研究进行了大鼠抗sars - cov -2多克隆抗体(pAb)的生产和纯化。方法:采用PEG/NaCl沉淀法纯化病毒抗原。还研究了蔗糖缓冲法的效率,以产生更纯净的抗原。免疫后用硫酸铵沉淀(33%)、透析、离子交换层析纯化抗体。采用Western blotting和酶联免疫吸附试验(ELISA)验证抗体特异性。所有数据均采用SPSS软件进行分析。结果:随着PEG浓度的增加,病毒浓缩量增加。此外,蔗糖缓冲法提高了其纯度。此外,通过这些抗原诱导大鼠产生高滴度的pAb免疫反应,ELISA/western blot结果表明抗体-抗原相互作用合适。此外,离子交换色谱法是一种纯化IgG的合适方法。结论:本文提出了一种简单、廉价、质量较高的病毒全粒纯化方法。结果证实,这些抗原能在大鼠体内引起良好的免疫反应。获得的pAbs对SARS-CoV-2抗原具有良好的特异性。因此,本研究为病毒疫苗的开发提供了一种有前景的方法。
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来源期刊
Advanced pharmaceutical bulletin
Advanced pharmaceutical bulletin PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
2.80%
发文量
51
审稿时长
12 weeks
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