By Mark Waghorn via SWNS
Catching a cold protects against COVID-19, according to new research and could be why some people avoid getting the disease.
The discovery provides a blueprint for a second-generation, universal vaccine that would combat current and future variants - including Omicron.
Scientists found a cold triggers specific immune cells that reduce the risk of infection.
via GIPHY
The study was based on 52 Britons exposed toCOVID-19 - half of whom developedCOVID-19.
Those who did not had more T cells - the body's immune memory cells which were induced by other coronaviruses - such as the common cold.
"Being exposed to the SARS-CoV-2 virus doesn't always result in infection - and we've been keen to understand why,"said first author Dr. Rhia Kundu, of Imperial College London.
"We found high levels of pre-existing T cells, created by the body when infected with other human coronaviruses like the common cold, can protect againstCOVID-19 infection."
Participants lived with someone with PCR-confirmed SARS-CoV-2 - the virus that causes COVID-19.
They were tested at the outset and four and seven days later to determine if they developed an infection.
Blood samples were also taken to measure pre-existing T cells that also cross-recognize COVID-19 proteins.
There were significantly more in the 26 who did not become infected compared to the 26 who did.
Importantly, the immune cells attack internal proteins within the virus.
It offers a more effective vaccine target that could provide long-lasting protection
The researchers explained T cell responses persist longer than antibodies which wane within a few months.
Current vaccines only destroy the virus' spike protein on the surface.
"Our study provides the clearest evidence to date T cells induced by common cold coronaviruses play a protective role against SARS-CoV-2 infection,"said senior author Professor Ajit Lalvani, also from Imperial.
"These T cells provide protection by attacking proteins within the virus, rather than the spike protein on its surface.
"The spike protein is under intense immune pressure from vaccine-induced antibody which drives evolution of vaccine escape mutants.
"In contrast, the internal proteins targeted by the protective T cells we identified mutate much less.
"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.”
Designing vaccines able to activate T cells would stop COVID-19 far earlier if 'replication proteins' in its internal system can be disabled.
This would be a different approach - offering an additional layer of protection than other jabs.
"While this is an important discovery, it is only one form of protection. I would stress no one should rely on this alone,"Kundu said.
"Instead the best way to protect yourself against COVID-19 is to be fully vaccinated - including getting your booster dose."
The study in Nature Communications began in September 2020 when most people in the UK had neither been infected nor vaccinated.