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Soluble CD13 is a potential mediator of neutrophil-induced thrombogenic inflammation in SARS-CoV-2 infection
Pei-Suen Tsou, … , Jason S. Knight, David A. Fox
Pei-Suen Tsou, … , Jason S. Knight, David A. Fox
Published April 1, 2025
Citation Information: JCI Insight. 2025;10(9):e184975. https://doi.org/10.1172/jci.insight.184975.
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Research Article COVID-19 Immunology Infectious disease

Soluble CD13 is a potential mediator of neutrophil-induced thrombogenic inflammation in SARS-CoV-2 infection

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Abstract

The soluble variant of the ectopeptidase CD13 (sCD13), released from the cell surface by matrix metalloproteinase 14 (MMP14), is a potent pro-inflammatory mediator, displaying chemotactic, angiogenic, and arthritogenic properties through bradykinin receptor B1 (B1R). We revealed a link between sCD13 and amplified neutrophil-mediated inflammatory responses in SARS-CoV-2 infection. sCD13 was markedly elevated in patients with COVID-19 and correlated with disease severity and variants, ethnicity, inflammation markers, and neutrophil extracellular trap formation (NETosis). Neutrophils treated with sCD13 showed heightened NETosis and chemotaxis, which were inhibited by sCD13 receptor blockade. Meanwhile sCD13 did not induce platelet aggregation. Single-cell analysis of COVID-19 lungs revealed coexpression of CD13 and MMP14 by various cell types, and higher CD13 expression compared with controls. Neutrophils with high CD13 mRNA were enriched for genes associated with immaturity, though CD13 protein expression was lower. Histological examination of COVID-19 lungs revealed CD13-positive leukocytes trapped in vessels with fibrin thrombi. Flow cytometry verified the presence of B1R and a second sCD13 receptor, protease-activated receptor 4, on monocytes and neutrophils. These findings identify sCD13 as a potential instigator of COVID-19–associated NETosis, potentiating vascular stress and thromboembolic complications. The potent pro-inflammatory effects of sCD13 may contribute to severe COVID-19, suggesting that sCD13 and its receptors might be therapeutic targets.

Authors

Pei-Suen Tsou, Ramadan A. Ali, Chenyang Lu, Gautam Sule, Carmelo Carmona-Rivera, Serena Lucotti, Yuzo Ikari, Qi Wu, Phillip L. Campbell, Mikel Gurrea-Rubio, Kohei Maeda, Sharon E. Fox, William D. Brodie, Megan N. Mattichak, Caroline Foster, Ajay Tambralli, Srilakshmi Yalavarthi, M. Asif Amin, Katarina Kmetova, Bruna Mazetto Fonseca, Emily Chong, Yu Zuo, Michael D. Maile, Luisa Imberti, Arnaldo Caruso, Francesca Caccuri, Virginia Quaresima, Alessandra Sottini, Douglas B. Kuhns, Danielle Fink, Riccardo Castagnoli, Ottavia M. Delmonte, Heather Kenney, Yu Zhang, Mary Magliocco, Helen Su, Luigi Notarangelo, Rachel L. Zemans, Yang Mao-Draayer, Irina R. Matei, Mirella Salvatore, David Lyden, Yogendra Kanthi, Mariana J. Kaplan, Jason S. Knight, David A. Fox

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Figure 6

Divergent CD13 expression is observed in mature and immature neutrophils.

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Divergent CD13 expression is observed in mature and immature neutrophils...
(A) Reanalysis of single-cell RNA-Seq results generated from circulating human neutrophils (32) revealed that immature neutrophils have higher ANPEP expression. Dot plot of ANPEP, IFN, and neutrophil maturity genes for each neutrophil cluster, showing the average expression level and the percentage of cells expressing the gene in each cluster. (B) Gating scheme of flow cytometry analysis on mature and immature neutrophils isolated from whole blood. CD10+CD16hi defines mature neutrophils while CD10–CD16lo defines immature neutrophils. (C) Significantly higher expression of CD13 and lower expression of PAR4 were observed in mature neutrophils compared with immature neutrophils while B1R expression showed similar levels. Data generated from 5–10 healthy controls. Results are expressed as mean ± SD. **P < 0.01. Significance was determined by Wilcoxon’s test.

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