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Arkansas Researchers Find Potential Cause of 'Long Haul' COVID-19 Symptoms

Arkansas Researchers Find Potential Cause of 'Long Haul' COVID-19 Symptoms
University of Arkansas for Medical Sciences researchers have found a potential cause of the long-haul symptoms of COVID-19 patients.

A research team at the University of Arkansas for Medical Sciences has identified a potential cause of long-lasting symptoms experienced by COVID-19 patients, often referred to as 'long-haulers'.

At the heart of the team's findings is an antibody that shows up weeks after an initial infection and attacks and disrupts a key regulator of the immune system, said lead researcher John Arthur, M.D., Ph.D., professor and chief of the Division of Nephrology in the UAMS College of Medicine, Department of Internal Medicine.

As many as 30% of COVID-19 patients experience lingering fatigue, brain fog and shortness of breath. The cause of long COVID-19 has eluded scientists, but the UAMS team's discovery sheds important new light on the molecular-level mechanisms behind it.

"Everything that we've found is consistent with this antibody as the instigator of long COVID, so it's an exciting development," Dr. Arthur said.

The antibody creates problems for the immune system by attacking the angiotensin-converting enzyme 2 (ACE2). The ACE2 enzyme helps regulate the body's response to the virus by metabolizing a peptide that activates the immune system.

The attacking antibody interferes with ACE2's work, which makes the antibody a prime suspect for the long-lasting illness.

The multidisciplinary research team was brought together quickly this spring to test the hypothesis that developed through discussions between Arthur and UAMS' Terry Harville, M.D., Ph.D., a professor in the Department of Pathology and medical director of the Histocompatibility and Immunogenetics Laboratories.

Researchers tested plasma or serum for ACE2 antibodies in 67 patients in Arkansas and Oklahoma with known SARS-CoV-2 (the virus that causes COVID-19) and 13 with no history of infection. In 81% of blood samples from patients with a history of COVID-19, the samples had the antibody that attacked the ACE2. In participants with no history of COVID-19, no antibodies were created to attack the ACE2 enzyme.

"If we show that the whole hypothesis is right, that this interference of ACE2 really does cause long COVID, then it opens up many potential treatments," said Arthur. "There are medications that should work to treat them."

The next step would be to test the drugs that might relieve the symptoms people are having.

The Little Rock scientists published their findings this month in the journal, The Public Library of Science ONE (PLOS ONE).

"This is true team science," Arthur said. "We put together a great group of investigators that had never worked together to produce these very exciting results."

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