- Whole inactivated virus: You grow the bad virus in the laboratory then inactivate it with chemicals or other methods, rendering it harmless. This was the method Salk used for the polio vaccine. At the moment, a Chinese company, Sinovac, is in clinical trials using this method.
- Recombinant nanoparticle: You synthesize pieces of the virus protein and grow them in insect cells along with a special compound. The government has paid Novavax $1.6 billion to develop this vaccine.
- Gene-based vaccine: You take a bit of RNA or DNA from the virus then stitch it into the genes of a vector, such as the virus for the common cold. This method was used to make a vaccine for Ebola.
- Viral-gene snippet: You take a snippet of a viral gene (m/RNA) which can enter the human cell and induce it to make the virus’ spike protein. The resulting antibodies latch onto the spike proteins. A company called Moderna is using this approach and is in the first phase clinical trials.
Of course, the laboratories making the other vaccines must conduct a series of clinical trials to determine dosages, side effects, safety, and efficacy. Sinovac’s trials are encouraging, as are Moderna’s, although a few test subjects in Moderna’s trials have gotten sick, probably because of dosage issues. After the trials are complete, companies must then manufacture and distribute the vaccine, a process that normally takes years. To speed up the process, some companies are already preparing for production. This will be interesting.
For an introduction to this blog, see I Just Say No; for a list of blog topics, click the Topics tab.
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