Vaccine-induced T cells provide long-lasting immune response to Covid: study

An electron microscopy image of the Omicron variant of SARS-CoV-2
A transmission electron micrograph of negative-stained SARS-CoV-2 Omicron variant virions, false-coloured. Image: Dr Jason A. Roberts, Head of Electron Microscopy and Structural Virology at The Royal Melbourne Hospital's Victorian Infectious Diseases Reference Laboratory, Doherty Institute

The human body's T cells provide long-lasting memory against the virus following vaccination or infection from COVID-19, a study led by the Peter Doherty Institute for Infection and Immunity (Doherty Institute) has shown.

Published today in Nature Immunology, the study utilised new technology to track the T cell responses of people who had recovered from COVID-19 for 15 months and found there was a sustained level of these cells capable of recognising the SARS-CoV-2 spike protein.

Senior author and senior research fellow at the Doherty Institute Dr Jennifer Juno said despite an initial contraction of the immune response immediately following infection, the T cells stabilised at six months and remained level after 15 months of monitoring.

"Even though some parts of the immune response wane, we can now see that T cells recognising the virus are quite stable over time. After more than a year, they were still roughly 10-fold higher than someone who had never been exposed to the spike protein through infection or vaccination," Dr Juno said.

While B cells are responsible for producing the antibodies that recognise SARS-CoV-2, T cells play a crucial role in supporting the development of the B cell response. Without T cell help, B cells are unable to produce high amounts of antibodies that can bind to the virus and stop infection.

When individuals were re-exposed to the COVID-19 spike protein through vaccination, the part of the virus that enables SARS-CoV-2 to attach and enter cells in humans, the T cells quickly reactivated and increased in number.

"Vaccination boosted the levels of these T cells to be up to 30 times higher than they were before," Dr Juno said.

The team looked at people who had recovered from mild illness, as well as people who had been vaccinated.

"In general, we saw that the vaccines generate the same amount of T cells as someone who had been infected. We also saw that the third dose does an incredible job at re-activating those T cells and bringing the levels back up again," Dr Juno said.

The team utilised new technology called tetramers that help identify which T cells recognise the spike protein to undertake the research, resulting in more accurate findings.

"Usually we have to stimulate the cells in the lab before we can measure the T cell response. However, using tetramers, we can look at them straight from the blood samples, meaning we are getting a more accurate picture of what is happening," Dr Juno said.

The team are now looking at how these T cells react when breakthrough infections happen.

"We are looking at people who have been vaccinated, but then still catch COVID-19, and trying to understand whether the T cells are still being reactivated in the same way as we've seen with the vaccines and primary infections," Dr Juno said.

The study was conducted in collaboration with the laboratory of Professor Miles Davenport from the Kirby Institute.

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