Comparative Assessment of the Whole-cell Pertussis Vaccine Potency Using Serological and Intracerebral Mouse Protection Methods
Publish place: Archives of Razi Institute journal، Vol: 74، Issue: 2
Publish Year: 1398
نوع سند: مقاله ژورنالی
زبان: English
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JR_ARCHRAZI-74-2_001
تاریخ نمایه سازی: 6 دی 1402
Abstract:
One of the most important QC tests of whole-cell pertussis vaccine (WCPV) is potency test. In this regard, mouse protection test (MPT) is the current potency method, which is associated with severe animal distress and large variability in results. The purpose of this study was to assess Pertussis Serological Potency Test (PSPT) as a serological alternative method to intracerebral challenge in MPT assay. In the current study, the potency of three experimental batches of WCPV (۱, ۲, and ۳) and standard vaccine were compared using MPT and PSPT methods. In the MPT method, mice were immunized with tests and standard vaccines. After ۲ weeks, they were intracerebrally challenged with Bordetella pertussis strain (۱۸۳۲۳). The potency was calculated via parallel line analysis based on the numbers of survivors ۲ weeks after the challenge. Similar to MPT method, mice were immunized in the PSPT method and bled after ۴ weeks. In the next step, sera were titrated by ۱۸۳۲۳-WCP-ELISA assay and potency values were estimated via parallel line analysis. Pearson correlation test was used to measure the strength of association between MPT and PSPT assay results. The potency values of the experimental laboratory batches ۱, ۲, and ۳ in MPT assays were ۱۱.۱۴, ۵.۰۲, and ۴.۲۴ Iu/ml, whereas the obtained results of PSPT assays were ۱۰.۳۲, ۴.۱۱, and ۳.۰۶ Iu/ml, respectively. The correlation of MPT and PSPT results was ۰.۸۰۷. The findings of the present study demonstrated a significant correlation between MPT and PSPT results. The implementation of PSPT was more advantageous, compared to MPT due to its ethical approaches and less variability in results. The PSPT is a promising alternative method for intracerebral challenge. However, additional validation is needed to support the establishment of this method.
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Authors
D. Mohammadbagher
Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran
M. Noofeli
Department of Human Viral Vaccine Production, Razi Vaccine and Serum Research Institute, Agricultural Research, Education and Extension Organization, Karaj, Iran
G. Karimi
Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran
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