Authors
M Elizabeth Moss, Stephanie Pons, Luciana P Tavares, Yan Tang, Galit Alter, Elizabeth Karlson, Lindsey Baden, David R Walt, Bruce D Levy
Published in
iScience. Volume 29. Issue 11. Pages 117581. Nov 20, 2026. Epub Oct 14, 2026.
Abstract
Long COVID (LC) represents a failure of healthy resolution mechanisms for inflammation after SARS-CoV-2 infection. Dietary essential polyunsaturated fatty acids (PUFAs) and their downstream metabolites can orchestrate inflammation resolution, suggesting these pathways may be altered in LC. In this study, plasma samples from two independent participant cohorts totaling 106 participants (designated by chart review as LC or Recovered) were collected longitudinally in the 12 months following SARS-CoV-2 infection and analyzed by mass spectrometry for targeted PUFA metabolites. In the acute phase of SARS-CoV-2 infection, upregulation of PUFA metabolites downstream of 12-lipoxygenase was associated with later development of LC. In the months following infection, LC participants displayed uncoupling of PUFA-related lipid metabolism and altered lipoxygenase-driven metabolism over time compared to recovered participants. These results provide new mechanistic insights for the development of LC and suggest potential therapeutic strategies for this prevalent and debilitating disorder.
PMID:
42909166
Bibliographic data and abstract were imported from PubMed on 23 Oct 2026.
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