The study published in the journal Blood found that inflammation and blood clotting seen in very severe cases of covid-19 may be caused by the antibodies sent to fight the disease activating unnecessary platelet activity in the lungs
NEW DELHI :
Antibodies produced to protect against covid-19 may trigger increased function of platelets, which may be causing fatal blood clots in patients with severe disease, research done by University of Reading England has revealed.
Platelets are small cells found in blood which form clots to stop or prevent bleeding, but where platelets don’t function properly this can lead to serious health concerns such as strokes and heart attacks. The study published in the journal Blood found that inflammation and blood clotting seen in very severe cases of covid-19 may be caused by the antibodies sent to fight the disease activating unnecessary platelet activity in the lungs.
The study took antibodies produced to fight the coronavirus’s spike protein, from people with severe covid-19 infections, and cloned them in a lab. The team found that the small sugars found on the surface of these antibodies were different from antibodies separated from healthy individuals, and when those cloned antibodies were introduced in a lab to blood cells taken from healthy donors, there was an observed increase in platelet activity.
The study team also found that it was possible to reduce or stop platelets from responding in this way in the laboratory by treating blood with active ingredients from drugs known to either inhibit platelet function or immune responses. The findings suggest that it may be possible for drugs that are currently used to treat immune system problems to reduce or stop the cells from producing an exaggerated platelet response.
A trial led by Imperial College London and Imperial College Healthcare NHS Trust—called MATIS—is already testing these drugs in clinical trials with patients at hospital sites across the UK to see whether they will reduce serious clotting for hospitalized covid-19 patients.
The lab-based study of human cells provides key evidence to support the scientific basis for the MATIS trial, and, while no result has been reported yet from this clinical trial, the two teams will continue to work closely together as the clinical trial develops. “Until now, we have only had assumptions about why platelets involved in clotting were being activated during covid-19 infection. One way to think of what happens is that the immune response that is designed to protect you from the infection in some cases, particularly in severely ill patients, actually causes more damage. In this case, the antibodies produced to stop covid-19 from spreading, trigger infected cells to induce platelet activity that causes clotting even though there is no wound that needs healing," Professor Jon Gibbins, director of the Institute for Cardiovascular and Metabolic Research at the University of Reading said.
“We are particularly excited because our studies of platelets in the laboratory establishes important mechanisms that explain how and why dangerous blood clots may occur in severely ill covid-19 patients, and importantly, also provides clues as to how this may be prevented," Gibbins said.
Co-author Nichola Cooper, reader at Imperial College London and consultant haematologist at Imperial College Healthcare NHS Trust, who also designed and leads the MATIS trial said: “Early on in the covid-19 pandemic it was clear that the infection was causing an overwhelming immune response, including blood clotting, and that many of the more severe cases and deaths were related to this.
“Having been involved in early research around blood clotting related to inflammation, it occurred to me that the drugs we already use for other disorders could be easily accessible treatments for covid-19. We are yet to see results from the MATIS trial, so we do not yet know how these drugs will work in patients, but our hope is that we can both inhibit the inflammatory response and prevent severe disease and blood clots. It is exciting to see our collaboration with Reading backing our theory already and providing a solid scientific basis for clinical trials."
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