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使用简单的本土技术生产安全、高效且具有免疫原性的部分纯化无细胞百日咳疫苗。

Production of a safe, potent and immunogenic partially purified acellular pertussis vaccine using simple indigenous techniques.

作者信息

Gupta R K, Saxena S N, Sharma S B, Ahuja S

机构信息

Biological Standardization & Quality Control Division, Central Research Institute, Kasauli (H.P.), India.

出版信息

Dev Biol Stand. 1991;73:205-22.

PMID:1778314
Abstract

Partially purified acellular pertussis vaccine was prepared from Bordetella pertussis strains 10536, 134, Tohama and 509 using simple indigenously available techniques. The Stainer-Scholte (SS) medium with methylated-beta-cyclodextrin was the most suitable for production of acellular pertussis vaccine. For preparation of the vaccine, 5 day cultures of B. pertussis grown under stationary conditions at 35 degrees C were treated twice with ammonium sulphate and prospective protective antigens were extracted. The extracts contained pertussis toxin (PT), filamentous hemagglutinin and agglutinogens. These extracts were treated with formaldehyde and glutaraldehyde separately for detoxification of PT. The formaldehyde treatment of acellular preparations affected the potency and did not destroy the toxic effects of PT completely. Active PT was found in formaldehyde detoxified acellular pertussis vaccine (FDAPV) preparations by the Chinese hamster ovary (CHO) cell assay, the test for leucocytosis promoting factor (LPF) and the histamine sensitization (HS) test. The FDAPV preparations did not pass the mouse weight gain test (MWGT). The glutaraldehyde treatment had lesser adverse effects on potency than the formaldehyde treatment and the glutaraldehyde detoxified preparations did not show active PT by CHO cell assay, the test for LPF and the HS test. The mice tolerated high doses (up to four human doses) of GDAPV which passed the MWGT showing higher weight gains. Both FDAPV and GDAPV showed immunogenicity against agglutinogens and PT in mice. The GDAPV is a safe and potent vaccine. The total protein content of GDAPV was about 5 times lesser than that of whole cell pertussis vaccine.

摘要

使用简单的本地可得技术,从百日咳博德特氏菌菌株10536、134、Tohama和509制备了部分纯化的无细胞百日咳疫苗。含有甲基化-β-环糊精的施泰纳-朔尔特(SS)培养基最适合用于生产无细胞百日咳疫苗。为制备该疫苗,将在35摄氏度静止条件下培养5天的百日咳博德特氏菌培养物用硫酸铵处理两次,并提取预期的保护性抗原。提取物中含有百日咳毒素(PT)、丝状血凝素和凝集原。这些提取物分别用甲醛和戊二醛处理以对PT进行解毒。无细胞制剂的甲醛处理影响效力,且未完全消除PT的毒性作用。通过中国仓鼠卵巢(CHO)细胞试验、白细胞增多促进因子(LPF)试验和组胺致敏(HS)试验,在甲醛解毒的无细胞百日咳疫苗(FDAPV)制剂中发现了活性PT。FDAPV制剂未通过小鼠体重增加试验(MWGT)。戊二醛处理对效力的不利影响小于甲醛处理,且戊二醛解毒的制剂通过CHO细胞试验、LPF试验和HS试验未显示活性PT。小鼠能耐受高剂量(高达四个人用剂量)的戊二醛解毒无细胞百日咳疫苗(GDAPV),该疫苗通过了MWGT,显示出更高的体重增加。FDAPV和GDAPV在小鼠中均显示出针对凝集原和PT的免疫原性。GDAPV是一种安全有效的疫苗。GDAPV的总蛋白含量约为全细胞百日咳疫苗的五分之一。

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