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In recent years, parents have started questioning the advantages of vaccination, a preventive measure that has been used for years . Before you do this, read more about vaccine development and how this process is regulated and controlled.

After a pharmaceutical company receives approval to sell the vaccine, local and international laws strictly regulate its industrial production.

Culturing virus and bacteria

The viral and bacterial agents used for vaccines need to be grown on an industrial scale. For this, pharmaceutical companies use different methods: yeast, bacteria and cell cultures, bioreactors and primary cell cultures. These last can be chicken embryos or fertilized chicken eggs.

The influenza virus, for example, is grown in fertilized eggs.

These eggs are specially produced for biotechnological applications and have to comply with health and safety regulations that allow them to be used as culture media for the influenza virus.

For the process of culturing, several chemical reagents have to be used to get either the inactivated or attenuated form of the organisms, or the fragments that are required for the vaccine.

These chemicals are removed through a purification process, which assures the consumer that no toxic substances are left in the final product.

Adjuvants are usually added to vaccines. What are they? They are chemical reagents that enhance the response of the immune system towards the virus or bacteria present in the vaccine solution. Also, as any other drug, stabilisers are used to keep the vaccine effective for as long as possible.

The final step is the packaging of the vaccine, which is done in sterile containers, usually small crystal vials, which can be easily transported and stored under specific conditions.

All the production process of any vaccine is controlled by regulatory international standards of quality that make sure that the vaccine is effective, of a good quality and that it doesn’t cause any harm to the consumer.

How does a vaccine work?

To explain how a vaccine can activate our immune system and keep it alert in case of infection, we will take the influenza vaccine as an example. 

The influenza vaccine is made of fragments, or antigens, obtained from the influenza virus. When these antigens are in contact with the immune system of the vaccine receiver, they are recognized by the immune cells and start the production of antibodies.

Antibodies are proteins that are produced by immune cells and that are specific for each antigen that they recognize. For example, the influenza virus antigens trigger the production of antibodies against influenza, whereas the smallpox virus antigens trigger the production of antibodies, similar to the ones for influenza, but that only recognize the smallpox virus.

Because the vaccine is mimicking the effects that the real virus would have in our immune system, it is normal to feel flu like symptoms such as fever, after being vaccinated. When the immune system finishes building up immunity against influenza, it goes back to normal but keeps a record of the influenza virus infection.

In other words, the antibodies that were produced against the influenza virus stay in our bodies, as a memory system, which will know how to fight against the influenza virus in case of a real infection. 

As you can see, vaccine development is not an easy process. It takes several years to take a vaccine from the lab to the pre-clinical stage, and more years to have it tested in humans and to be approved for its production and commercialization. The process is strictly controlled from head to toe to make sure that it helps in preventing the spread of diseases, such as the flu and tuberculosis, without putting in danger the health and safety of us as consumers. 

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