Immunological memory provides long-term protection against coronavirus

Immunological memory provides long-term protection against coronavirus

Many questions about how exposure to SARS-CoV-2 by infection or immunization might result in long-term protective immunity remain unanswered. Onur Boyman, head of the Department of Immunology, and his research team at the University of Zurich and the University Hospital Zurich, have now taken a closer look at how this long-lived protection is formed. Together with researchers from ETH Zurich, they identified specific signaling pathways that determine when immune cells develop into so-called memory T cells.

From short-lived killers to long-term memory T cells

Virus-specific antibodies produced by B cells are insufficient to effectively protect against the novel coronavirus. The cellular immune response to SARS-CoV-2 is just as important. Here, virus-specific CD8+ T cells play a crucial role, as they can identify and kill the cells that have been infected by the virus. These cytotoxic T cells eliminate viruses that are hidden inside the host cells and help prevent the spread of millions of newly formed viruses. “These T cells are usually active for only a short time and disappear quickly. When it comes to establishing long-term protective immunity, it is important to generate long-lived memory T cells that are activated very quickly upon re-exposure to the virus,” explains Onur Boyman. This latter ability is referred to as immunological memory.

Previous studies have focused on the whole CD8+ T cell population that formed in response to the virus. Boyman and his team have now succeeded in tracking individual clones of SARS-CoV-2-specific CD8+ T cells in patients with COVID-19, from the acute viral infection up to one year after recovery. The researchers were also able to identify the signaling pathways responsible for the transition of CD8+ T cells from short-lived killers to long-lived memory cells—and they found a distinct molecular signature.

Immune messengers determine the cell type

In their study, the researchers were able to demonstrate that the signature of long-lived memory CD8+ T cells was already present during acute SARS-CoV-2 infection, and these cells could thus be distinguished from their short-lived counterparts at an early stage. “The distinct signature of memory cells contained signals of immune messengers, such as interferons, which are an important part of the immune response against SARS-CoV-2 and also contribute to controlling viral infections,” says Onur Boyman.

Immune response varies from one patient to another

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