Whoah, lipid-coated mRNA vaccines, not as an intermediate step but as the actual delivery method? That’s actually new to me! Sounds like it’s mRNAs coding for some subset of the viral proteins, which probably get assembled into proteins in your cells and then get used as something for antibodies to respond against. mRNAs should then just degrade themselves with time.
I have no idea what the most efficient method for producing those is; I am very used to vaccines being protein-based. This probably is in the realm where it’s simple enough that modifying PCR-protocols to produce RNA instead might actually work reasonably well, although RNA is generally more fragile and error-prone and that could be a problem.
You’d be using nucleotides, not amino acids, but mRNA from DNA is a short-enough assembly line that you might not need cells to do it.
(Protein production has a lot of dependencies. mRNA transcription should basically just require your DNA of interest, nucleotides (x4), and a transcriptase protein. Maybe add a transcription factor or two.)
HeLa definitely is a human cell line (although that was for Ebola, they may end up using a different cell line). That’s good, that probably scales up easily.
“Disease X could emerge suddenly and have deadly consquences—we’ve seen this happen with Ebola, MERS coronavirus, Zika, and countless other diseases. That’s why we’re striving to develop rapid-response vaccine platforms—like CureVac’s mRNA technology—to defend against these unknown pathogens. CEPI has now established partnership agreements totaling more than $50 million in three such platforms”.
It seems that the third mRNA vaccine company is BioNTech.
Johnson & Johnson appears to be using a more traditional approach in which the virus is inactivated so it can’t replicate but can still express viral proteins. The approach takes a little longer for both the development and manufacturing scale-up steps. On the plus side, Johnson & Johnson’s slow-but-steady approach could create a vaccine with a better immune response.
There’s a forth company with Inovio Pharm that also develops a COVID-19 vaccine. It’s technology is based on delievering DNA based.
I have the impression that the mRNA/DNA ways of vaccine delievery allow for faster development of a vaccine then the old fashioned protein based way.
Whoah, lipid-coated mRNA vaccines, not as an intermediate step but as the actual delivery method? That’s actually new to me! Sounds like it’s mRNAs coding for some subset of the viral proteins, which probably get assembled into proteins in your cells and then get used as something for antibodies to respond against. mRNAs should then just degrade themselves with time.
I have no idea what the most efficient method for producing those is; I am very used to vaccines being protein-based. This probably is in the realm where it’s simple enough that modifying PCR-protocols to produce RNA instead might actually work reasonably well, although RNA is generally more fragile and error-prone and that could be a problem.
You’d be using nucleotides, not amino acids, but mRNA from DNA is a short-enough assembly line that you might not need cells to do it.
(Protein production has a lot of dependencies. mRNA transcription should basically just require your DNA of interest, nucleotides (x4), and a transcriptase protein. Maybe add a transcription factor or two.)
HeLa definitely is a human cell line (although that was for Ebola, they may end up using a different cell line). That’s good, that probably scales up easily.
From last year: From CEPI awards US$ 34M contract to CureVac to advance The RNA Printer™
It seems that the third mRNA vaccine company is BioNTech.
It seems that Johnson & Johnson is still developing a vaccine the traditional way:
There’s a forth company with Inovio Pharm that also develops a COVID-19 vaccine. It’s technology is based on delievering DNA based.
I have the impression that the mRNA/DNA ways of vaccine delievery allow for faster development of a vaccine then the old fashioned protein based way.