Non-human primate model of long-COVID identifies immune associates of hyperglycemia.
Clovis S PalmerChrysostomos PerdiosMohamed Abdel-MohsenJoseph MuddPrasun K DattaNicholas J ManessGabrielle LehmickeNadia GoldenLinh HellmersCarol CoyneKristyn Moore GreenCecily MidkiffKelsey M WilliamsRafael TiburcioMarissa FahlbergKyndal BoykinCarys KenwayKasi E Russell-LodrigueAngela BirnbaumRudolf BohmRobert V BlairJason P DufourTracy FischerAhmad A SaiedJay RappaportPublished in: Nature communications (2024)
Hyperglycemia, and exacerbation of pre-existing deficits in glucose metabolism, are manifestations of the post-acute sequelae of SARS-CoV-2. Our understanding of metabolic decline after acute COVID-19 remains unclear due to the lack of animal models. Here, we report a non-human primate model of metabolic post-acute sequelae of SARS-CoV-2 using SARS-CoV-2 infected African green monkeys. Using this model, we identify a dysregulated blood chemokine signature during acute COVID-19 that correlates with elevated and persistent hyperglycemia four months post-infection. Hyperglycemia also correlates with liver glycogen levels, but there is no evidence of substantial long-term SARS-CoV-2 replication in the liver and pancreas. Finally, we report a favorable glycemic effect of the SARS-CoV-2 mRNA vaccine, administered on day 4 post-infection. Together, these data suggest that the African green monkey model exhibits important similarities to humans and can be utilized to assess therapeutic candidates to combat COVID-related metabolic defects.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- liver failure
- respiratory failure
- endothelial cells
- coronavirus disease
- drug induced
- type diabetes
- traumatic brain injury
- chronic obstructive pulmonary disease
- gene expression
- dna methylation
- adipose tissue
- metabolic syndrome
- extracorporeal membrane oxygenation
- big data
- weight loss
- glycemic control