LONDON (Reuters) – High levels of T-cells from common cold coronaviruses can provide protection against COVID-19, an Imperial College London study published on Monday has found, which could inform approaches for second-generation vaccines.
Immunity against COVID-19 is a complex picture, and while there is evidence of waning antibody levels six months after vaccination, T-cells are also believed to play a vital role in protecting against illness.
The new research suggests that cross-reactive T-cells may also protect against infection.
The study, which began in September 2020, looked at levels of cross-reactive T-cells generated by previous common-cold coronavirus infections in 52 household contacts of positive COVID-19 cases shortly after exposure, to see if they went on to test positive for SARS-CoV-2.
It found that the 26 who did not develop infection had significantly higher levels of those memory T-cells than people who did get infected. Imperial did not say how long protection from the T-cells would last.
“We found that high levels of pre-existing T cells, created by the body when infected with other human coronaviruses like the common cold, can protect against COVID-19 infection,” study author Dr Rhia Kundu said.
The authors of the study, published in Nature Communications, said that the internal proteins of the SARS-CoV-2 virus which are targeted by the T-cells could offer an alternative target for vaccine makers.
Current COVID-19 vaccines target the spike protein, which mutates regularly, creating variants such as Omicron which lessen the efficacy of vaccines against symptomatic infection.
“In contrast, the internal proteins targeted by the protective T-cells we identified mutate much less,” Professor Ajit Lalvani, co-author of the study, said.
“Consequently, they are highly conserved between the various SARS-CoV-2 variants, including Omicron. New vaccines that include these conserved, internal proteins would therefore induce broadly protective T cell responses that should protect against current and future SARS-CoV-2 variants.”
SOURCE: https://go.nature.com/3ndsPub Nature Communications, online January 10, 2022.