Why most people who get COVID have mild symptoms or none at all while some become severely ill is still a mystery – a mystery that scientists are urgently trying to solve.
Being obese or having existing health problems, such as diabetes or high blood pressure, are known to increase the risk of severe COVID. But this is not the whole story. Some seemingly healthy people can suffer from severe disease, too.
Early in 2020, scientists discovered that people with severe COVID had unusual levels of certain immune cells in their blood. They included cells that are “first responders”, such as natural killer cells, as well as cells that develop after infection and specifically target cells infected with coronavirus, such as T cells. Scientists also discovered that these patients have changes in some cytokines – proteins that orchestrate the immune response.
In severe COVID, the checks and balances that usually control the immune system seem to be altered. But the damage to the body’s organs is not caused by the virus itself but by the immune system’s response to the virus. Finding out who is at risk of this runaway immune response, before symptoms kick in, is important.
A new study, which has yet to be published in a scientific journal, sheds some light on the matter. The researchers, from the University of Cambridge, found that very early changes in the immune response to the virus could be used to predict who will develop severe disease and who won’t.
The scientists took 605 blood samples from 207 people with COVID and 45 healthy controls and measured their immune responses over 90 days. At the end of the study, they compared the immune responses of people who experienced severe COVID with people who suffered from mild disease or were asymptomatic.
They found that early in the infection, the immune systems of people with severe COVID produced higher levels of inflammatory cytokines, such as TNF-alpha, compared to people with mild disease. The people with severe disease also had fewer immune cells that are known to specifically target the virus, such as T cells and B cells. In other words, early in infection, the people with severe disease had lower numbers of immune cells that could target the virus and they had higher levels of inflammation.
In the blood of the worst affected people, the scientists observed changes in their immune responses at about the time of symptom onset – well before they were admitted to a hospital. They examined over 30 different immune cell types and found that these changes occurred in perhaps 13 different cell subsets.
The researchers also showed that the people worst affected by the disease had higher levels of inflammation at the point that their symptoms developed. Many of these changes persisted in the most severely ill patients 60 days after their symptoms started.
On the other hand, patients with mild disease or no symptoms were found to mount an early and robust adaptive immune response to the virus. An adaptive immune response is where the immune system identifies an infection and then produces T cells, B cells and antibodies specific to the virus to fight back.
These people produced the immune components in the first week of infection and in larger numbers than people who experienced more severe COVID. After the infection was cleared, the number of immune cells that responded to the virus rapidly returned to normal. There was no evidence in these people of systemic inflammation that can lead to organ damage.
People who develop severe disease have a slower immune response to the virus. By the time they develop symptoms, their immune response is measurably different from those with mild disease. Crucially, these changes could be used to predict disease outcome.
These findings may have major implications for managing patients already known to be at risk of severe COVID. If it was possible to screen and diagnose high-risk people early, before the onset of symptoms, drugs could be given to prevent the immune system changes that contribute to severe disease. It is also possible that these persisting changes in the immune system could provide insight into how long COVID develops.
ABOUT THE AUTHOR
Rebecca Aicheler is a Senior Lecturer in Immunology, Cardiff Metropolitan University. Aicheler’s research passion lies with understanding what regulates the function of Natural Killer (NK) cells. NK cells constitute a heterogeneous population of innate lymphocytes that exhibit an extraordinary capacity to kill tumour cells and control certain viral infections. NK cells are able to act independently of specific antigen recognition making them a key constituent of the innate immune response. Their function is regulated by integrating a combination of activating and inhibitory signals received from ligands on their targets and my research questions focus on understanding how these signals regulate NK cell function.