The German company BioNTech partnered with Pfizer to develop and test a coronavirus vaccine known as BNT162b2. A clinical trial demonstrated that the vaccine has an efficacy rate of 95 percent in preventing Covid-19.
A piece of coronavirus
The Sars-CoV-2 virus is studded with proteins that it uses to enter human cells. These so-called spike proteins make a tempting target for potential vaccines and treatments.
Like the Moderna vaccine, the Pfizer-BioNTech vaccine is based on the virus’s genetic instructions for building the spike protein.
mRNA inside an oily shell
The vaccine uses messenger RNA, genetic material that our cells read to make proteins. The molecule, called mRNA for short, is fragile and would be chopped to pieces by our natural enzymes if it were injected directly into the body. To protect their vaccine, Pfizer and BioNTech wrap mRNA in oily bubbles made of lipid nanoparticles.
Because of their fragility, the mRNA molecules will quickly fall apart at room temperature. Pfizer is building special containers with dry ice, thermal sensors and GPS trackers to ensure the vaccines can be transported at -70 Celsius to stay viable.
Entering a cell
After injection, the vaccine particles bump into cells and fuse to them, releasing mRNA. The cell’s molecules read its sequence and build spike proteins. The mRNA from the vaccine is eventually destroyed by the cell, leaving no permanent trace.
Some of the spike proteins form spikes that migrate to the surface of the cell and stick out their tips. The vaccinated cells also break up some of the proteins into fragments, which they present on their surface. These protruding spikes and spike protein fragments can then be recognised by the immune system.
Spotting the intruder
When a vaccinated cell dies, the debris will contain many spike proteins and protein fragments, which can then be taken up by a type of immune cell called an antigen-presenting cell.
The cell presents fragments of the spike protein on its surface. When other cells called helper T-cells detect these fragments, the helper T-cells can raise the alarm and help marshal other immune cells to fight the infection.
Making antibodies
Other immune cells, called B-cells, may bump into the coronavirus spikes and protein fragments on the surface of vaccinated cells. A few of the B-cells may be able to lock on to the spike proteins. If these B-cells are then activated by helper T-cells, they will start to proliferate and pour out antibodies that target the spike protein.
Stopping the virus
The antibodies can latch on to coronavirus spikes, mark the virus for destruction and prevent infection by blocking the spikes from attaching to other cells.
Killing infected cells
The antigen-presenting cells can also activate another type of immune cell called a killer T-cell to seek out and destroy any coronavirus-infected cells that display the spike protein fragments on their surfaces.
Remembering the virus
The Pfizer-BioNTech vaccine requires two injections, given 21 days apart, to prime the immune system well enough to fight off coronavirus. But because the vaccine is so new, researchers don’t know how long its protection might last.
A preliminary study found that the vaccine seems to offer strong protection about 10 days after the first dose, compared with people taking a placebo.
It’s possible that in the months after vaccination, the number of antibodies and killer T-cells will drop. But the immune system also contains special cells called memory B-cells and memory T-cells that might retain information about the coronavirus for years or even decades.
Preparation and injection
Each vial of the vaccine contains 5 doses of 0.3 millilitres. The vaccine must be thawed before injection and diluted with saline. After dilution the vial must be used within six hours. – New York Times
