Abstract

The only currently available live vaccine against yellow fever (YF) based on chicken embryos infected with an attenuated 17D strain of the YF virus is one of the most effective vaccine preparations. However, the live vaccine is associated with "viscerotropic syndrome" (approximately 0.4 cases per 100 000 vaccinated). Therefore, the development and introduction of highly purified inactivated vaccine against YF is intended to ensure the maximum safety of vaccination against one of the most common human viral diseases.Goals and objectives. Development and evaluation of immunogenicity of the cultural inactivated vaccine against YF at the laboratory model level. Adaptation of 17D strain of YF virus to Vero cell culture, cultivation, removal of cellular DNA, inactivation with β-propiolactone, concentration, chromatographic purification, determination of protein and antigen of YF virus, assessment of immunogenicity in mice in parallel with commercial live vaccine. Immunogenicity: the determination of specific antibodies of class G (IgG) and virus neutralizing antibodies in the sera of immunized mice showed high level of antibodies exceeding that of immunized with commercial live vaccine. The optimal dose of antigen in the vaccine (total protein) was 50 μg/ml (5 μg/0.1 ml -dose and volume per 1 vaccination of mice). Thus, the laboratory version of cultural inactivated vaccine against YF is as effective (and even superior) as the commercial live vaccine. Laboratory version of cultural inactivated vaccine against YF, which is not inferior in immunogenicity (in animal model) to commercial live vaccine, has been developed.

Highlights

  • The only currently available live vaccine against yellow fever (YF) based on chicken embryos infected with an attenuated 17D strain of the YF virus is one of the most effective vaccine preparations

  • The development and introduction of highly purified inactivated vaccine against YF is intended to ensure the maximum safety of vaccination against one of the most common human viral diseases

  • Immunogenicity: the determination of specific antibodies of class G (IgG) and virus neutralizing antibodies in the sera of immunized mice showed high level of antibodies exceeding that of immunized with commercial live vaccine

Read more

Summary

Разработка инактивированной культуральной вакцины против жёлтой лихорадки

Цель исследования – разработка и оценка иммуногенности культуральной инактивированной вакцины против ЖЛ на уровне лабораторной модели. В ходе исследования проведены адаптация штамма 17D вируса ЖЛ к культуре клеток Vero, культивирование, удаление клеточной ДНК, инактивация β-пропиолактоном, концентрирование, хроматографическая очистка, определение белка и антигена вируса ЖЛ, оценка иммуногенности на мышах параллельно с коммерческой живой вакциной. Лабораторный вариант культуральной инактивированной вакцины против ЖЛ по эффективности не уступает коммерческой живой вакцине и даже превосходит её. Разработан лабораторный вариант культуральной инактивированной вакцины против ЖЛ, не уступающий по иммуногенности (на модели животных) коммерческой живой вакцине. Для цитирования: Иванов А.П., Клеблеева Т.Д., Рогова Ю.В., Иванова О.Е. Разработка инактивированной культуральной вакцины против жёлтой лихорадки. – концепция, эксперименты, анализ данных, написание статьи; Клеблеева Т.Д. – анализ данных, написание и редактирование текста.

Introduction
Material and methods
Материал и методы
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call