Post by Nadica (She/Her) on Dec 5, 2024 3:40:09 GMT
Biological Mechanisms Underlying Severe COVID-19 - Published Dec 4, 2024
Severe COVID-19 has been considered an inflammatory “cytokine storm” condition.
Severe COVID-19 arises in part from the SARS-CoV-2 virus’s impact on mitochondria, tiny oxygen-burning power plants in cells, which can help trigger a cascade of organ- and immune system-damaging events, suggests a study by investigators at Weill Cornell Medicine, Johns Hopkins Medicine, Children’s Hospital of Philadelphia, and the University of Pittsburgh School of Medicine, along with other members of the COVID-19 International Research Team.
Severe COVID-19 has been considered an inflammatory “cytokine storm” condition in which the immune response to a viral infection becomes excessive, flooding the bloodstream and tissues with immune signaling proteins at levels that cause lung-impairing inflammation and other signs and symptoms.
The new study, published Nov. 27 in PNAS, extends the scientific understanding of the molecular pathways driving this storm. By using RNA sequencing and other laboratory techniques on patient and animal model tissue samples, the investigators were able to examine these processes in great detail. Weill Cornell Medicine researchers, led by Dr. Robert Schwartz, associate professor of medicine, provided much of the deidentified patient material, including nasopharyngeal swabs and autopsied organ samples, as well as COVID-19 animal models, and contributed to their analysis.
The teams’ findings show that SARS-CoV-2 virus infection can cause significant damage to mitochondria in infected cells—damage that activates the immune system, contributing to the storm of inflammatory and other responses.
Prominent among these responses, the researchers noted, is the overactivation of a blood-pressure-regulating system called the renin-angiotensin-activation-system (RAAS). The overactive RAAS is associated with abnormal blood clotting—a striking feature of severe COVID-19—and, the researchers noted, with scarring-like abnormalities in lymph nodes, and dysfunctions of the immune cells found within them. The latter, the researchers say, may account for the impaired immune function that is also seen in severe COVID-19.
“One of the suggestions of these findings is that there is, early in the process, profound mitochondrial dysfunction and damage, which is then driving RAAS overactivation, which in turn contributes to the multi-organ damage of severe COVID-19,” said Dr. Schwartz, who is also a hepatologist at NewYork-Presbyterian/Weill Cornell Medical Center. “In addition, we’re concerned that these processes underlying acute COVID-19 may not always return to normal afterwards.”
The researchers are currently investigating this possibility in cases of “long COVID,” a syndrome that features lingering inflammation as well as immune cell dysfunction.
Reference: Topper MJ, Guarnieri JW, Haltom JA, et al. Lethal COVID-19 associates with RAAS-induced inflammation for multiple organ damage including mediastinal lymph nodes. PNAS. 2024. doi: 10.1073/pnas.2401968121
www.pnas.org/doi/10.1073/pnas.2401968121
Severe COVID-19 has been considered an inflammatory “cytokine storm” condition.
Severe COVID-19 arises in part from the SARS-CoV-2 virus’s impact on mitochondria, tiny oxygen-burning power plants in cells, which can help trigger a cascade of organ- and immune system-damaging events, suggests a study by investigators at Weill Cornell Medicine, Johns Hopkins Medicine, Children’s Hospital of Philadelphia, and the University of Pittsburgh School of Medicine, along with other members of the COVID-19 International Research Team.
Severe COVID-19 has been considered an inflammatory “cytokine storm” condition in which the immune response to a viral infection becomes excessive, flooding the bloodstream and tissues with immune signaling proteins at levels that cause lung-impairing inflammation and other signs and symptoms.
The new study, published Nov. 27 in PNAS, extends the scientific understanding of the molecular pathways driving this storm. By using RNA sequencing and other laboratory techniques on patient and animal model tissue samples, the investigators were able to examine these processes in great detail. Weill Cornell Medicine researchers, led by Dr. Robert Schwartz, associate professor of medicine, provided much of the deidentified patient material, including nasopharyngeal swabs and autopsied organ samples, as well as COVID-19 animal models, and contributed to their analysis.
The teams’ findings show that SARS-CoV-2 virus infection can cause significant damage to mitochondria in infected cells—damage that activates the immune system, contributing to the storm of inflammatory and other responses.
Prominent among these responses, the researchers noted, is the overactivation of a blood-pressure-regulating system called the renin-angiotensin-activation-system (RAAS). The overactive RAAS is associated with abnormal blood clotting—a striking feature of severe COVID-19—and, the researchers noted, with scarring-like abnormalities in lymph nodes, and dysfunctions of the immune cells found within them. The latter, the researchers say, may account for the impaired immune function that is also seen in severe COVID-19.
“One of the suggestions of these findings is that there is, early in the process, profound mitochondrial dysfunction and damage, which is then driving RAAS overactivation, which in turn contributes to the multi-organ damage of severe COVID-19,” said Dr. Schwartz, who is also a hepatologist at NewYork-Presbyterian/Weill Cornell Medical Center. “In addition, we’re concerned that these processes underlying acute COVID-19 may not always return to normal afterwards.”
The researchers are currently investigating this possibility in cases of “long COVID,” a syndrome that features lingering inflammation as well as immune cell dysfunction.
Reference: Topper MJ, Guarnieri JW, Haltom JA, et al. Lethal COVID-19 associates with RAAS-induced inflammation for multiple organ damage including mediastinal lymph nodes. PNAS. 2024. doi: 10.1073/pnas.2401968121
www.pnas.org/doi/10.1073/pnas.2401968121