SPUTNIK V
- October 18, 2020
- Posted by: OptimizeIAS Team
- Category: DPN Topics
No Comments
Subject: Science and tech
Context : Pharma Major Dr. Reddy’s Laboratories have received approval for trials in India.
Concept :
- The vaccine has been called Sputnik V, named after the first artificial Earth satellite, Sputnik-I launched by the Soviet Union.
- It is the first Covid-19 vaccine to be approved.
- The vaccine is based on the DNA of a SARS-CoV-2 type adenovirus, a common cold virus.
- The vaccine uses the weakened virus to deliver small parts of a pathogen and stimulate an immune response.
- The vaccine is administered in two doses and consists of two types of a human adenovirus, each carrying an S-antigen of the new coronavirus, which enter human cells and produce an immune response.
Adenovirus Vector Vaccine:
- In this vaccine, adenovirus is used as a tool to deliver genes or vaccine antigens to the target host tissue.
- Adenovirus: Adenoviruses (ADVs) are DNA viruses ranging from 70-90 nanometre in size, which induces many illnesses in humans like cold, respiratory infection etc.
- Adenoviruses are preferred for vaccines because their DNA is double stranded which makes them genetically more stable and the chances of them changing after injection are lower.
- Rabies vaccine is an adenovirus vaccine.
- However, there are drawbacks of adenovirus vector vaccines like pre-existing immunity in humans, inflammatory responses etc.
- Just as human bodies develop immune responses to most real viral infections, they also develop immunity to adenoviral vectors. Since adenoviral vectors are based on natural viruses that some humans might already have been exposed to, these vaccines might not work for everyone.
Use in India:
- Russia has claimed that around 20 countries have shown interest in the Sputnik V vaccine, including India..
- The approval for a vaccine is given by the Central Drugs Standard Control Organisation (CDSCO).
- The Central Drugs Standard Control Organisation (CDSCO), under Directorate General of Health Services ,Ministry of Health & Family Welfare, is the National Regulatory Authority (NRA) of India.
- Under the Drugs and Cosmetics Act, 1940, CDSCO is responsible for approval of Drugs, Conduct of Clinical Trials, laying down the standards for Drugs, control over the quality of imported Drugs in the country and coordination of the activities of State Drug Control Organizations by providing expert advice.