The South African Health Products Regulatory Authority, or SAHPRA, said in a statement Tuesday that the request for Sputnik V to be authorized could “not be approved at this time,” referring to past failed HIV vaccines that used a similar technology.
A late-stage study published in the journal Lancet last year in more than 20,000 participants found that Sputnik V was safe and about 91% effective in preventing people from becoming severely ill with COVID-19.
Sputnik V uses two types of harmless viruses known as adenoviruses to carry the spike protein into the body, which then primes the immune system to produce antibodies against COVID-19. SAHPRA said concerns have been raised about the safety of Adenovirus Type 5, which is used in one of the Sputnik V doses. The other dose contains Adenovirus Type 26, which is also used by Johnson & Johnson.
South African officials pointed to two failed research studies testing an HIV vaccine also using Adenovirus Type 5, which found men who were vaccinated had a higher risk of being infected with HIV. The regulators said they had asked the Russian makers of Sputnik V to provide data proving the vaccine's safety in a country with high rates of HIV but that “the applicant was not able to adequately address (their) request.”
“It's a strange connection to make,” he said, explaining that while past concerns have been raised about using the particular virus vector in Sputnik V, much remains uncertain. “It's not the vector that caused HIV so you can't just blame it on that,” Tang said.
The vaccine made by AstraZeneca uses a related chimpanzee adenovirus; both it and the Johnson & Johnson shot have been approved in South Africa.
The Russian makers of Sputnik V, the Gamaleya Institute, couldn't immediately be reached for comment. Amid widespread vaccine hesitancy in Russia, authorities have struggled to convince people to get vaccinated and the immunization rate in the country has remained stubbornly low, at about 32%, despite availability of Sputnik V.
Sputnik V is currently also being considered for authorization by the World Health Organization and the European Medicines Agency. The shot has been given the green light in more than 70 countries. To date no significant safety problems have been identified.
AP Medical Writer Maria Cheng reported from London.
Follow all AP stories on the coronavirus pandemic at https://apnews.com/hub/coronavirus-pandemic.
Register for free to continue reading
Registration is a free and easy way to support our truly independent journalism
By registering, you will also enjoy limited access to Premium articles, exclusive newsletters, commenting, and virtual events with our leading journalists
Already have an account? sign in