治疗制品

兔抗新型冠状病毒血清制备中佐剂对抗体效价的影响

  • 胡云光 ,
  • 英志芳 ,
  • 张玉平 ,
  • 殷安国 ,
  • 李亚东 ,
  • 常亚军 ,
  • 段男 ,
  • 易力 ,
  • 宋杰
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  • 1中国医学科学院&北京协和医学院医学生物学研究所,昆明 650031;2国家药品监督管理局疫苗及生物制品质量控制与评价重点实验室,成都 611731;3中国食品药品检定研究院,国家卫生健康委员会生物技术产品检定方法及其标准化重点实验室,北京 102629

网络出版日期: 2025-08-16

基金资助

云南省重大科技专项(202102AA100057)

Effects of adjuvants in rabbit anti-SARS-CoV-2 serum preparation on the antibody titer

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  • 1Institute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Kunming 650031, China; 2NMPA Key Laboratory for Quality Control and Evaluation of Vaccines and Biological Products, Chengdu 611731, China; 3National Institute for Food and Drug Control, Key Laboratory of Research on Quality and Standardization of Biotech Products, National Health Commission, Beijing 102629, China

Online published: 2025-08-16

Supported by

Science and Technology Major Project of Yunnan Province (202102AA100057)

摘要

目的  制备高效价兔抗新型冠状病毒血清并研究佐剂对抗体效价的影响。方法  将9只新西兰兔随机分为a、b、c组,分别皮下注射新型冠状病毒混合弗氏佐剂、氢氧化铝佐剂或单磷酰脂A佐剂进行免疫,0、28、42 d各免疫1次。每次免疫前及初次免疫后14 d于耳中央动脉采血,初次免疫后49 d经颈动脉采血,分离血清,进行中和抗体效价检测以及中和试验。结果  经过整个免疫程序后,a、b、c组均能产生高效价抗血清,且a组(6 144.00)最终产生的血清中和抗体效价高于b组(4 437.33)、c组(3 754.67);3组血清均可在中和试验中有效中和KMS2株新型冠状病毒,中和后培养细胞均未发生病变。结论  3种不同佐剂疫苗在新西兰兔体内均可产生高水平的免疫应答。

本文引用格式

胡云光 , 英志芳 , 张玉平 , 殷安国 , 李亚东 , 常亚军 , 段男 , 易力 , 宋杰 . 兔抗新型冠状病毒血清制备中佐剂对抗体效价的影响[J]. 国际生物制品学杂志, 2023 , 46(3) : 146 -150 . DOI: 10.3760/cma.j.cn311962-20220927-00063

Abstract

Objective  To preparate high-efficacy rabbit anti-severe acute respiratory syndrome coronavirus 2(SARS-CoV-2) serum and to study the effect of different adjuvants in rabbit anti-SARS-CoV-2 serum preparation on the antibody titer. Methods  Nine New Zealand rabbits were randomly divided into groups a, b, and c, and were immunized by subcutaneous injections with SARS-CoV-2 mixed with Freund's adjuvant, aluminum hydroxide adjuvant, or monophosphoryl lipid A adjuvant, respectively. They were immunized 3 times on 0, 28, and 42 d. Blood samples were collected from the central ear artery before every immunization, and at 14 d after the first immunization. Blood was also collected from the carotid artery on 49 d after the first immunization to separate the serum for neutralizing antibody titer detection and neutralizing tests. Results  After the entire immunization process, all groups produced highly effective anti-SARS-CoV-2 serum. Group a (6 144.00) had a higher final neutralizing antibody titer than groups b (4 437.33) and c (3 754.67). The serum obtained from all 3 groups could effectively neutralize the KMS2 strain of SARS-CoV-2 in neutralizing tests without causing any cell damage. Conclusion  All 3 different adjuvants can be used to obtain highly effective anti-SARS-CoV-2 serum in New Zealand rabbits.
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