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Anti–miR-93-5p therapy prolongs sepsis survival by restoring the peripheral immune response
Mihnea P. Dragomir, … , Sai-Ching Yeung, George A. Calin
Mihnea P. Dragomir, … , Sai-Ching Yeung, George A. Calin
Published June 1, 2023
Citation Information: J Clin Invest. 2023;133(14):e158348. https://doi.org/10.1172/JCI158348.
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Research Article Immunology Infectious disease

Anti–miR-93-5p therapy prolongs sepsis survival by restoring the peripheral immune response

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Abstract

Sepsis remains a leading cause of death for humans and currently has no pathogenesis-specific therapy. Hampered progress is partly due to a lack of insight into deep mechanistic processes. In the past decade, deciphering the functions of small noncoding miRNAs in sepsis pathogenesis became a dynamic research topic. To screen for new miRNA targets for sepsis therapeutics, we used samples for miRNA array analysis of PBMCs from patients with sepsis and control individuals, blood samples from 2 cohorts of patients with sepsis, and multiple animal models: mouse cecum ligation puncture–induced (CLP-induced) sepsis, mouse viral miRNA challenge, and baboon Gram+ and Gram– sepsis models. miR-93-5p met the criteria for a therapeutic target, as it was overexpressed in baboons that died early after induction of sepsis, was downregulated in patients who survived after sepsis, and correlated with negative clinical prognosticators for sepsis. Therapeutically, inhibition of miR-93-5p prolonged the overall survival of mice with CLP-induced sepsis, with a stronger effect in older mice. Mechanistically, anti–miR-93-5p therapy reduced inflammatory monocytes and increased circulating effector memory T cells, especially the CD4+ subset. AGO2 IP in miR-93–KO T cells identified important regulatory receptors, such as CD28, as direct miR-93-5p target genes. In conclusion, miR-93-5p is a potential therapeutic target in sepsis through the regulation of both innate and adaptive immunity, with possibly a greater benefit for elderly patients than for young patients.

Authors

Mihnea P. Dragomir, Enrique Fuentes-Mattei, Melanie Winkle, Keishi Okubo, Recep Bayraktar, Erik Knutsen, Aiham Qdaisat, Meng Chen, Yongfeng Li, Masayoshi Shimizu, Lan Pang, Kevin Liu, Xiuping Liu, Simone Anfossi, Huanyu Zhang, Ines Koch, Anh M. Tran, Swati Mohapatra, Anh Ton, Mecit Kaplan, Matthew W. Anderson, Spencer J. Rothfuss, Robert Silasi, Ravi S. Keshari, Manuela Ferracin, Cristina Ivan, Cristian Rodriguez-Aguayo, Gabriel Lopez-Berestein, Constantin Georgescu, Pinaki P. Banerjee, Rafet Basar, Ziyi Li, David Horst, Catalin Vasilescu, Maria Teresa S. Bertilaccio, Katayoun Rezvani, Florea Lupu, Sai-Ching Yeung, George A. Calin

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Figure 5

Identification of miR-93-5p target genes in sepsis and miR-93-5p upstream regulation.

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Identification of miR-93-5p target genes in sepsis and miR-93-5p upstrea...
(A) Schematic of the AGO2 IP method. Beads coupled to anti-AGO2 antibody or control (IgG) antibody are used to pull down the RISC complex including bound miRNA/mRNA interactors in the presence or absence of miR-93 expression. Putative miR-93 targets (n = 579) were defined as being enriched in the AGO2 IP of parental or control cells but not miR-93–KO cells. (B) Pathway analysis on 570 putative miR-93 target genes showed strong enrichment for previously known mRNA targets (miRTarBase) of miR-93 or other miR-17 family members that share the same seed sequence. The top 9 most enriched are shown. (C) Forty-three genes with immune functions that were identified in the AGO2 IP and validated (purple) or predicted (black) targets of miR-93-5p were assessed in JURKAT miR-93–KO cells compared with control by RT-qPCR. Bars indicate the mean fold change (FC) in gene expression in the KO 1 and KO 2 samples relative to control (control = 1). (D) STAT1 protein expression measured by Western blotting in cell lysates of JURKAT shControl, JURKAT shSTAT1_A, and shSTAT1_B cells. (E) STAT1 mRNA expression, (F) IL4 mRNA expression, and (G) miR-93-5p measured by RT-qPCR in JURKAT shControl, and JURKAT shSTAT1_A, and shSTAT1_B cells.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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