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05.01.2023 14:04

How COVID-19 permanently damages the heart

Stefan Zorn Stabsstelle Kommunikation
Medizinische Hochschule Hannover

    MHH research team shows for the first time how the inflammation in COVID 19 alters the smallest vessels in the heart

    Severe courses of COVID-19 infection not only impair lung function, but can also cause life-threatening consequences for the heart. The spectrum ranges from acute inflammation of the heart muscle (myocarditis) to chronic restriction of the heart's pumping function. The basic patterns of damage have not yet been completely proven. An interdisciplinary research team led by Professor Dr. Danny Jonigk, Christopher Werlein and Private Lecturer (PD) Dr. Mark Kühnel from the Institute of Pathology at the Hannover Medical School (MHH) has now used innovative molecular methods and a high-resolution microscopy technique to show how the ongoing inflammation in COVID-19 attacks the heart tissue and, in the long term, remodels the smallest coronary vessels by directing special precursor cells of the immune system from the blood into the heart. The study was published in the renowned journal Angiogenesis.

    False-activated inflammatory cells

    About one in three people complain of discomfort and functional impairment of the heart after severe COVID-19 disease. In order to elucidate the mechanisms of this long-lasting myocardial damage, the researchers examined heart tissue from patients with severe COVID 19 and compared it with tissue samples taken after severe influenza infections caused by the influenza virus and after severe myocarditis caused by other viruses. Although in the COVID 19 heart injury - unlike the comparison samples - there was no classic inflammation of the heart tissue on the outside, the research team did find a large accumulation of false-activated inflammatory cells: so-called macrophages and their precursor cells, the monocytes. "These monocytes have an outstanding importance as precursor cells of new blood vessel formation and can remodel the blood vessel system in a very short time," explains Christopher Werlein, first author of the study.

    COVID-19 attacks all vessels in the body

    Triggered by the infection with the coronavirus SARS-CoV-2, tiny blockages accumulate in the heart vessels, which are only a few millimetres thick. "These ultra-thrombi change the blood flow considerably and thus also the oxygen supply", emphasises PD Dr. Kühnel. This calls the monocytes into action, which attach themselves to the inner vessel walls and form new branches there. This vascular remodelling - known as intussusceptive angiogenesis - has already been described by the team as a characteristic pattern of damage in other organs of COVID 19 patients. What may be intended as a short-term rescue response by the body to compensate for reduced blood flow and undersupply of oxygen could lead to chronic damage to the heart and long covid, the researchers suspect. "In any case, the latest investigations confirm our earlier assumption that SARS-CoV-2 systemically attacks all vessels in the body and remodels them in the long term," Professor Jonigk emphasises.

    The work was done in cooperation with the German Center for Lung Research (DZL) at the Hannover BREATH site, the University Hospital Aachen, the University Medical Center Mainz and the Georg-August University Göttingen.

    SERVICE:

    The original paper "Inflammation and vascular remodelling in COVID-19 hearts" can be found here: https://link.springer.com/article/10.1007/s10456-022-09860-7

    For further information, please contact PD Dr Mark Kühnel, kuehnel.mark@mh-hannover.de, telephone (0511) 532-4492.


    Bilder

    The photomontage shows PD Dr. Mark Kühnel (left) and Christopher Werlein at a multitasking microscope with a tissue section of the heart vessels remodelled by COVID-19.
    The photomontage shows PD Dr. Mark Kühnel (left) and Christopher Werlein at a multitasking microscop ...

    Copyright: Karin Kaiser/Fig.: Image rendering courtesy Siemens Healthineers 2022, data courtesy UCL's ESRF Beamtime MD1290


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