Affiliation:
1. Crucell Holland BV, Archimedesweg 4–6, PO Box 2048, 2301 CA Leiden, The Netherlands
Abstract
Background: As most vaccines exert their protective capacity by eliciting pathogen-specific antibodies, antibody assays assessing immunogenicity of vaccines in development should be well characterized. Part of the validation of immunogenicity assays for vaccines is the study of stability of antibodies in serum. Materials & methods: Stability of antibodies in human serum was assessed by circumsporozoite-binding IgG ELISA designed for assessing the immunogenicity of a malaria vaccine under development, adenovirus neutralization assay, designed to assess neutralizing antibodies against adenovirus and commercially available test kits for hepatitis A and B. Results: Stability studies indicated stability of serum-binding IgG antibodies and serum-neutralizing antibodies in: long-term storage below -65°C and -20°C; short-term storage; multiple freeze/thaw rounds; during shipment; and during heat inactivation. Conclusion: Results have shown the stability of both binding and functional polyclonal antibodies in human serum under stable storage and common usage circumstances.
Subject
Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry
Reference15 articles.
1. Correlates of Protection Induced by Vaccination
2. Challenges of immunogenicity assays for vaccines
3. US Department of Health and Human Services, US FDA, Center for Drug Evaluation and Research (CDER), Center for Veterinary Medicine. Guidance for Industry – Bioanalytical Method Validation. (2001). www.fda.gov/downloads/Drugs/Guidances/ucm070107.pdf
4. EMA. Guideline on bioanalytical method validation. EMEA/CHMP/EWP/192217/2009. EMA, London, UK (2012).
Cited by
21 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献