Revolutionary plasmid DNA shot, given using 'gene gun', is new weapon against SARS-CoV-2
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DNA is the blueprint of life. Our genes, made up of DNA, determine how cells reproduce. Genes define heredity. What’s fascinating is that some genes have also proven to act as “instructions” to make molecules, such as proteins.
That, in a nutshell, is the idea behind DNA-based vaccines. Until today, no other DNA vaccine has been approved anywhere — except ZyCoV-D, developed in India and now authorised by drug regulators in the sub-continent. About a dozen other vaccine candidates using the plasmid DNA platform are on trial in different parts of the world. But the approval of ZyCoV-D signals a breakthrough in medical science, a "new wave" in vaccinology.
What we know so far:
A DNA vaccine uses a copy of a genetic sequence from a part (i.e. outer or spike-protein) of a pathogen (virus or bacteria) to stimulate the body’s immune system. More specifically, it known as “plasmid DNA vaccine”.
Yes. ZyCoV-D was developed by Indian pharmaceutical company Zydus Cadila, based in Ahmedabad, with support from India’s Biotechnology Industry Research Assistance Council (BIRAC). It was approved by India’s drug regulator on August 20, 2021.
ZyCoV-D is India’s second home-grown vaccine — the first being Covaxin, developed by Bharat Biotech jointly with the Indian Council of Medical Research (ICMR) and the National Institute of Virology (NIV).
67%, based on interim data analysis. VE is defined as "protection against symptomatic COVID-19". This efficacy is essentially against the now-dominant Delta variant (trials were conducted in India, where Delta was first reported).
Zydus Cadila applied for approval in July 2021. Following a month-long review, the Drug Controller General of India (DCGI) approved ZyCoV-D on August 20, 2021.
3 doses are required to achieve efficacy, according to Zydus Cadila.
People aged 12 and older.
Pricing has not been announced. Indian media reported Zydus expects $27.2 to $34 million (Rs200-250 crore) in monthly sales from ZyCoV-D.
The immunogenicity figure of 67% is based on initial data readout of the Phase 3 trial involving 28,000 volunteers: 21 symptomatic cases of COVID-19 were detected in the vaccinated group and 60 among people who received a placebo, Nature reported. Included in the trial were adolescents in the 12-18 age group.
No. Full results of the late-stage trials (Phase III) are yet to be published. The full analysis will be submitted for publication “shortly”, Zydus Cadila told Indian media.
Zydus plans to make up to 120 million doses of ZyCoV-D per year. The company says the first doses will start to be administered in India this month (September).
India has so far given more than 570 million doses of three previously approved vaccines — Covishield, Covaxin and Sputnik V — with about 13% of adults now fully vaccinated, while 47% have received at least one shot since January.
Vaccines developed using other platforms, particularly mRNA, had a comparatively higher initial VE, upwards of 90%. Those were developed and trialled before new variants emerged.
ZyCoV-D’s 67% efficacy, on the other hand, was recorded from trials in the midst of a Delta-dominant pandemic in India. The variant has shown an immune-escape capability, thus reducing VE of other vaccines from their initially high levels. The most significant fact is that ZyCoV-D is a DNA vaccine, say scientists.
Dr Paul Offit, the co-inventor of a rotavirus vaccine, explained in a video published December 2, 2020:
“The way this strategy (DNA vaccine) works is you take a small gene from the virus, the gene that codes for this so-called SARS-CoV-2 spike protein…It’s the protein responsible for attaching the virus to (human) cells. If you can make antibodies to that protein that attaches the virus to cells then, presumably, you can prevent the virus from attaching to cells. Or said another way, you can prevent the virus from infecting you.”
In short, when you get a DNA shot for COVID-19, it uses the replication mechanism in your own cells to make the spike protein.
No. The DNA vaccine encodes only a specific spike protein of SARS-CoV-2 — not the virus’ entire genome. When the immune system recognises the target protein gene as being foreign to the body, it triggers an immune response.
Vaccines differ in a number of ways: their composition and how they trigger an immune response. Most of the anti-COVID vaccines approved today are made of the following:
The crucial thing with DNA shots are the plasmids — and therein lies the key challenge. For plasmids to work, they have to make it all the way to the cell nucleus, unlike mRNA vaccines, which just need to get to the cytoplasm, Shahid Jameel, a virologist at Ashoka University in Sonipat, India, told the journal Nature.
As with the mRNA and attenuated (live-virus) vaccines, the body’s immune system recognises and mounts defences against self-generated S-protein molecules coded by the DNA shot. In case of a subsequent infection, the body’s inner defences have developed an army of antibodies.
CELL CYTOPLASM VS CELL NUCLEUS
• The cytoplasm is the semifluid substance of a cell outside the nuclear membrane but within the cellular membrane. • The nucleus is inside a fully enclosed nuclear membrane and contains most of the cell's genetic material. • Some of the components of the nucleus: nuclear envelope, nuclear lamina, nucleolus, chromosomes, nucleoplasm — they all work for the nucleus to accomplish all of its functions.
By “deposition” under the skin. It’s also called a “needle-free” vaccine. The DNA is administered using a “gene gun” pressed against the skin, which creates a fine, high-pressure stream of fluid that punctures the surface.
Investigations into the use of DNA as a vaccine platform tarted more than 60 years ago. In 1960, Dr. Yoichiro Ito, a Japanese scientist, first reported the property of DNA to get “transfected” to mammalian cells in vivo (in a living organism). In 1993, the first DNA vaccine — applied to poultry — was directed against avian influenza virus (AIV). DNA vaccines had been approved for use in animals, such as horses, too.
However, until recently, they have not demonstrated robust immune response in human trials. In recent months, vaccines have undergone “warp-speed” development as governments funded the trials due to the pandemic-driven urgency. The ease of enrolment of thousands of subjects, thanks to the internet, has also helped accelerate trials.
DNA vaccines offer a number of benefits, including:
“GENE GUN”
• DNA-coated particle bombardment — aka “biolistics” or “gene gun” or “micro-projectile bombardment and particle acceleration” — was first introduced in 1987 to deliver DNA, RNA or protein from outside (exogenous) to cells. • A “gene gun” is quite versatile, as the device can transform almost any type of cell.
1) Experimental stage: Initial attempts to create DNA vaccines have not worked – they have not had a big enough impact on the immune system.
2) Unproven: Before India’s approval of Cadila Healthcare’s ZyCoV-D vaccine, no DNA vaccine has been licensed for use in humans (though dozens of DNA vaccines are now in clinical trials).
PLASMID
Plasmid comes from the words “cytoplasm" and “id” (“it” in Latin). At the most basic level, plasmids are small, circular pieces or molecules of DNA that replicate independently from the host chromosomal DNA. Compared to the millions or billions of bases that make up the entire genome, plasmids typically contain thousands at most. Some of the advantages of plasmids: • They’re relatively small • Stable • Easy to manipulate
In nature, they’re found in microbes, like bacteria. In 1952, Nobel laureate Joshua Lederberg and his collaborators at the University of Wisconsin first used to the term “plasmid” as a generic term for any extrachromosomal genetic particle. He used it to describe "any extrachromosomal hereditary element” in a paper he published describing some experiments he and his graduate student Norton Zinder conducted on Salmonella bacteria and its virus P22.
Since the 1940s, scientists have found that there are “heritable” cytoplasmic factors that could be transferred between cells. Occasionally, plasmids that are linear, or made of RNA, exist. They may be found as single or multiple copies and may carry from half a dozen to several hundred genes.
Plasmids can only multiply inside a host cell. Most plasmids inhabit bacteria: around 50% of bacteria found in the wild contain one or more plasmids. Plasmids are also found in higher organisms such as yeast and fungi. The 2-micron circle of yeast is a well-known example that has been modified for use as a cloning vector.
There are currently 12 in various clinical trial phases in Japan, South Korea, Thailand, Australia, Italy, US and Canada, in addition to India.
The approval of ZyCoV-D as the world’s first DNA vaccine is a key moment in medical science. There are yet unanswered questions:
It would be interesting to watch what happens next. What's clear is that, after more than 60 years, extensive research on plasmid DNA vaccines has finally paid off. And if they do prove their worth in the real world, experts say DNA vaccines, alongside gene guns, could altogether transform vaccinology.
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