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The Lancet publishes results [PDF] of Russian COVID-19 vaccine clinical trials

Sputnik has spoken to the vaccine developers at the Gamaleya Centre, Alexander Gintsburg and Denis Logunov, as well as the CEO of the Russian Direct Investment Fund Kirill Dmitriev, to find out what data the article cites and why it is so important for the global scientific community.

Today, less than a month after the Sputnik V COVID-19 vaccine was registered, the world’s most influential scientific journal The Lancet has published the results of the first two stages of clinical trials, so highly-anticipated by both the Russian and international scientific community.

The article responds to foreign criticism and provides long-awaited clarity. The Russian scientists’ development, which turned out to be the world’s first registered coronavirus vaccine, is not only effective but safe.

Start of a Series of Publications

The Lancet has published the results [PDF] of the first two stages of clinical trials and, according to the vaccine developers at the Gamaleya Centre, this is going to be the first step towards a series of publications about the Sputnik V vaccine in scientific journals.

“In September, a complete study of the vaccine in animals, primates, Syrian hamsters, transgenic mice, in which the vaccine has shown 100% protective efficacy (results in primates and Syrian hamsters were obtained before clinical trials), will be published. The first results of the ongoing post-registration clinical trial involving 40,000 volunteers will be published in October-November”.

‘Vaccine With Proven Safety’

The Sputnik V vaccine’s safety is one of the main conclusions cited in the article. According to the first and second-stage clinical trial results, the scientists didn’t find any serious adverse effects from the vaccine regarding any of the evaluated criteria. Not all candidate vaccines can boast of such results, some have noted up to 25% experiencing serious adverse effects.

Long-Term Immunity

The Lancet also cites scientific evidence of the Sputnik V vaccine’s effectiveness. For example, evidence of the treatment’s ability to launch a long-term immune response to the coronavirus in 100% of those vaccinated due to its unique two-stage introduction technology. According to Denis Logunov, deputy research director at the Gamaleya Centre, a humoral and cellular immune response, which is enough to protect a person from COVID-19, has been observed in 100% of those vaccinated.

“The antibody levels in vaccinated volunteers was 1.4-1.5 times higher than in those who had recovered. For reference, Britain’s AstraZeneca vaccine showed an antibody level roughly equal to the antibody level in those who had had the coronavirus infection”.
Scientists at the Gamaleya Centre confirm that in the context of Sputnik V clinical trials, all of the volunteers developed T-cell immunity, represented by both CD4+ and CD8+ cells, making it possible to recognise and destroy coronavirus-infected cells.

‘The Vaccine Will Work in 100% of Cases’

One of the scientific community’s biggest fears regarding the use of human adenoviral vector vaccines — the technology used in Sputnik V — was the pre-existing immunity to adenoviruses in some people.

In other words, there was a concern that our immunity might not allow the required amount of human adenovirus into the body. This serves as a kind of “taxi” in the vaccine, delivering the outer shell genetic material of the coronavirus into the cells (it’s important that the coronavirus itself doesn’t enter the body with the vaccine, which completely eliminates the possibility of infection).

Due to people often getting sick with adenoviruses (like the common cold), they could have developed immunity, which theoretically could reduce the adenovirus vaccine’s effectiveness. However, the results of the trials presented by the Gamaleya Centre scientists prove otherwise: pre-existing immunity doesn’t affect the vaccine’s effectiveness.

“We’ve chosen the optimal safe dosage, providing an effective immune response in 100% of those vaccinated, including those who have recently had adenovirus infections. This reduces the urgency of developing new vaccines based on untested platforms”.

According to the representatives of the Gamaleya Centre, what is meant by unverified platforms are developments of some Western companies, that started out of concerns regarding human adenoviruses. Some of these developments, such as mRNA technology (Moderna’s vaccine) or chimpanzee adenovirus (AstraZeneca’s vaccine), have never been used to create registered vaccines.

Such drugs need long-term testing because of concerns regarding their effect on the body’s reproductive functions or the possible high carcinogenic properties that lead to cancer, the centre concluded.

In the article, Russian scientists refer to studies about the safety of the platform on which the Sputnik V vaccine is based.

“Since 1953, more than 250 clinical trials have been carried out globally, and more than 75 international articles have been published confirming the safety of vaccines and drugs based on this platform”, Denis Logunov explained.
“Human adenoviral vectors-based drugs have been used for over 15 years. In particular, these are Ebola vaccines and the anti-cancer Gendicine, which has been used in China for over 12 years”.

Unique Two-Vector Technology

According to Alexander Gintsburg, Sputnik V’s unique feature is using two adenoviruses, serotypes 5 and 26, in two separate vaccinations. Today, many experts recognise double vaccination as a factor that can significantly enhance immunity to the coronavirus.

However, if the same vector is used for two vaccinations, the immune system triggers defence mechanisms and begins rejecting the second-injection drug. This problem is solved by using two vectors in Sputnik V, which helps avoid the described neutralising effect.

Gamaleya vs AstraZeneca

Responding to criticism about the insufficient number of volunteers for the two-vector vaccine, the scientists recalled that they managed to test this system on a wider range of people than, for example, one of the leading vaccine candidates, AstraZeneca, did.

The British pharmaceutical giant used four times fewer volunteers during the first two trial stages to determine their two-vector vaccine’s effectiveness.

“The number of volunteers involved in testing the Russian Sputnik V vaccine during stages 1 and 2, carried out with two injections, was 4 times higher than the number of people AstraZeneca involved”, Kirill Dmitriev said.

‘The Only Safe Technology’

Last week, the US Food and Drug Administration announced the possible use of accelerated registration for vaccine candidates due to the current epidemiological situation, without a third phase of clinical trials on tens of thousands of volunteers.

The British authorities also spoke about the possibility of a similar approach. At the same time, according to these countries’ regulators, accelerated registration will only be possible for vaccines that have already proven their effectiveness and safety.

According to Russian specialists, there are not very many drugs that meet these requirements.

“To date, the only one meeting these criteria is a human adenoviral vector platform. It has proven its safety through several decades of numerous studies”, Kirill Dmitriev said.
The Lancet Publication is the ‘Final Answer’

Kirill Dmitriev, CEO of the Russian Direct Investment Fund, explained that The Lancet’s publication of the clinical trial results [PDF] is “the final answer in the round of questions directed against Russia” following the Sputnik V’s registration in August.

“In turn, Russia can now ask some questions to the international community. We are calling to publishing official data that would prove the long-term efficacy of chimpanzee adenovirus or mRNA-based vaccines, the absence of any carcinogenic risks and effects on fertility when used. We would also like to know why AstraZeneca is pushing for a legal disclaimer for unwanted side effects”.

Source: SPUTNIK