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SARS-CoV-2 spike protein expression as an identification in quality control testing for Adenovector based COVID-19 vaccine.
Kasana, Harit; Ade, Ajay Kumar; Meena, Jaipal; Sayal, Archana; Sheikh, Faraz; Anvikar, Anupkumar R; Chander, Harish.
Afiliação
  • Kasana H; National Institute of Biologicals, Plot No. A-32, Sector-62, Noida, Uttar Pradesh 201309, India.
  • Ade AK; National Institute of Biologicals, Plot No. A-32, Sector-62, Noida, Uttar Pradesh 201309, India.
  • Meena J; National Institute of Biologicals, Plot No. A-32, Sector-62, Noida, Uttar Pradesh 201309, India.
  • Sayal A; National Institute of Biologicals, Plot No. A-32, Sector-62, Noida, Uttar Pradesh 201309, India.
  • Sheikh F; National Institute of Biologicals, Plot No. A-32, Sector-62, Noida, Uttar Pradesh 201309, India.
  • Anvikar AR; National Institute of Biologicals, Plot No. A-32, Sector-62, Noida, Uttar Pradesh 201309, India.
  • Chander H; National Institute of Biologicals, Plot No. A-32, Sector-62, Noida, Uttar Pradesh 201309, India.. Electronic address: drharish.chander@nib.gov.in.
J Immunol Methods ; 529: 113680, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38703946
ABSTRACT

AIM:

Quality control testing of the vaccine for lot release is of paramount importance in public health. A recent pandemic caused by the SARS-CoV-2 virus brought together all spheres of vaccine to combat the virus. The scientific advancement in the development of vaccines facilitated the scientists to develop the vaccine against SARS-CoV-2 in a record time. Thus, these vaccines should be stringently monitored for their safety and efficacy as per the latest WHO and national regulatory guidelines, and quality control evaluation of the product should be done at national control laboratories before releasing the product into the market as it assures the quality and safety of the vaccine.

METHODS:

The SARS-CoV-2 exploited the ACE2 (Angiotensin Converting Enzyme 2) receptor, a surface protein on mammalian cells to gain entry into the host cells. The viral surface protein that interacted with the ACE2 receptor is the Spike protein of SARS-CoV-2. Thus, in the development of the vaccine and assessing its quality, the Spike protein of SARS-CoV-2 became an attractive immunodominant antigen. In National Institute of Biologicals, an apex body in the testing of biologicals in India, received the Adenovector (Adenovirus + vector) based COVID-19 vaccine, a finished product for quality evaluation. Due to the lack of a pharmacopeial monograph, the testing of the vaccine was done as per the manufacturer's specifications and methods. The routine assays of identification employed by the manufacturer do not reflect the expression of Spike protein which is required for the immune system to get activated. In this report, we showed the determination of Spike protein expression by immunoblotting and immunofluorescence for identification parameters in the quality testing of the COVID-19 vaccine. We determined the translation of the SARS-CoV-2 Spike gene cloned into an Adenovector.

RESULTS:

The results from these experiments indicated the expression of Spike protein upon infection of mammalian cells with viral particles suggested that the expression of immunodominant Spike protein of SARS-CoV-2 may be employed by quality control laboratories as a parameter for identification.

CONCLUSION:

The study suggested that the determination of the expression of Spike protein is pertinent to identifying the Adenovector based vaccines against COVID-19.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Controle de Qualidade / Glicoproteína da Espícula de Coronavírus / Vacinas contra COVID-19 / SARS-CoV-2 Limite: Animals / Humans Idioma: En Revista: J Immunol Methods Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Índia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Controle de Qualidade / Glicoproteína da Espícula de Coronavírus / Vacinas contra COVID-19 / SARS-CoV-2 Limite: Animals / Humans Idioma: En Revista: J Immunol Methods Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Índia