WHO Working Group on revision of the Manual of Laboratory Methods for Testing DTP Vaccines—Report of two meetings held on 20–21 July 2006 and 28–30 March 2007, Geneva, Switzerland
| Autor: | Dorothy K.L. Xing, Yoshinobu Horiuchi, R. Dobbelaer, Rose Gaines Das, Michael J. Corbel, Dianliang Lei |
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| Rok vydání: | 2008 |
| Předmět: |
Laboratory methods
Pediatrics medicine.medical_specialty Dtp vaccine General Veterinary General Immunology and Microbiology Standardization business.industry Public Health Environmental and Occupational Health Infectious Diseases Who recommendations Control test Molecular Medicine Medicine Statistical analysis Medical physics business Safety testing Control methods |
| Zdroj: | Vaccine. 26:1913-1921 |
| ISSN: | 0264-410X |
| DOI: | 10.1016/j.vaccine.2008.02.013 |
| Popis: | Summary This report reflects the discussion and conclusions of a WHO group of experts from National Regulatory Authorities (NRAs), National Control Laboratories (NCLs), vaccine industries and other relevant institutions involved in standardization and control of diphtheria, tetanus and pertussis vaccines (DTP), held on 20–21 July 2006 and 28–30 March 2007, in Geneva Switzerland for the revision of WHO Manual for quality control of DTP vaccines. Taking into account recent developments and standardization in quality control methods and the revision of WHO recommendations for D, T, P vaccines, and a need for updating the manual has been recognized. In these two meetings the current situation of quality control methods in terms of potency, safety and identity tests for DTP vaccines and statistical analysis of data were reviewed. Based on the WHO recommendations and recent validation of testing methods, the content of current manual were reviewed and discussed. The group agreed that the principles to be observed in selecting methods included identifying those critical for assuring safety, efficacy and quality and which were consistent with WHO recommendations/requirements. Methods that were well recognized but not yet included in current Recommendations should be taken into account. These would include in vivo and/or in vitro methods for determining potency, safety testing and identity. The statistical analysis of the data should be revised and updated. It was noted that the mouse based assays for toxoid potency were still quite widely used and it was desirable to establish appropriate standards for these to enable the results to be related to the standard guinea pig assays. The working group was met again to review the first drafts and to input further suggestions or amendments to the contributions of the drafting groups. The revised manual was to be finalized and published by WHO. |
| Databáze: | OpenAIRE |
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