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Updated: Aug 2, 2025

Analysis of Human T Cell Activity in an Allogeneic Co-Culture Setting of Pre-Treated Tumor Cells
Published on: March 7, 2025
Immunometabolic interference between cancer and COVID-19
Francesca Maria Consonni1,2, Barbara Durante2, Marcello Manfredi3,4
1Department of Pharmaceutical Sciences, University of Piemonte Orientale "A. Avogadro", Novara, Italy.
Cancer patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection exhibit immunometabolic dysregulation. This involves altered immune cells, depleted tryptophan, and reduced nicotinamide adenine dinucleotide (NAD+), worsening COVID-19 outcomes.
Area of Science:
- Immunometabolism
- Oncology
- Infectious Diseases
Background:
- Cancer patients face higher risks for severe coronavirus disease 2019 (COVID-19).
- Mechanisms linking cancer, metabolic disorders, and COVID-19 severity remain unclear.
- Immunometabolic pathways may offer insights into cancer patient vulnerability to SARS-CoV-2.
Purpose of the Study:
- To identify immunometabolic pathways common to cancer and SARS-CoV-2 infection.
- To investigate how cancer influences the immune and metabolic status of COVID-19 patients.
Main Methods:
- Utilized a combined flow cytometry and multiomics approach.
- Analyzed circulating myeloid and lymphoid immune cell subsets.
- Assessed tryptophan metabolites, nicotinamide adenine dinucleotide (NAD+) levels, and cytokine expression in peripheral blood mononuclear cells (PBMCs).
Main Results:
- COVID-19 cancer patients showed altered immune cell frequencies and activation.
- Observed depletion of tryptophan and tryptamine, accumulation of kynurenines, and low NAD+ availability.
- PBMCs displayed downregulated IL-6 and upregulated IFNγ mRNA expression.
Conclusions:
- Cancer exacerbates the metabolic dysregulation in COVID-19 patients.
- Impaired NAD+-dependent immune homeostasis contributes to increased COVID-19 severity in cancer patients.
- Findings highlight the critical role of immunometabolism in cancer patient outcomes during the pandemic.
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