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Updated: May 2, 2026
Single-cell Analysis of Immunophenotype and Cytokine Production in Peripheral Whole Blood via Mass Cytometry
Published on: June 26, 2018
Decoding monocyte heterogeneity in sepsis: a single-cell apoptotic signature for immune stratification and guiding
Wenjuan Duan1,2, Qi Chen2,3, Wei Li2,4
1Department of Pulmonary and Critical Care Medicine, First Affiliated Hospital of Chengdu Medical College, Chengdu, Sichuan, China.
Background:
The effectiveness of immunomodulatory therapies in sepsis is often hampered by profound and patient-specific immune heterogeneity. Classical monocytes play a central role in the progression toward sepsis-induced immunoparalysis, with their apoptotic rate serving as a sensitive marker of immune dysfunction. Traditional bulk transcriptomic approaches fail to resolve this complexity. Here, we harness single-cell RNA sequencing to delineate the apoptotic landscape of classical monocytes and identify robust molecular biomarkers for immunological stratification and targeted intervention.
Methods:
We integrated single-cell and bulk transcriptomic data from four independent cohorts. A machine learning pipeline incorporating SVM, RF, XGB, and GLM algorithms was used to identify hub genes associated with monocyte apoptosis. A diagnostic nomogram was constructed based on the selected gene signature and validated across external datasets. Clinical relevance was confirmed through Western blot analysis of purified monocytes from sepsis patients and healthy controls.
Results:
A four-gene signature (G0S2, GZMA, ITM2A, PAG1) emerged as a specific apoptotic fingerprint of classical monocytes. The diagnostic model based on these signature genes demonstrated excellent discriminatory performance, effectively stratifying patients into high-risk and low-risk groups (AUC >0.8 across multiple validation cohorts), with each risk group exhibiting distinctly different immune states. High-risk patients exhibited a pro-inflammatory transcriptomic profile with elevated apoptotic pathway activity (e.g., neutrophil degranulation), whereas the low-risk group showed enrichment in adaptive immunity and T cell receptor signaling. Protein-level validation in clinical samples corroborated the transcriptomic findings.
Conclusion:
This study elucidates a critical facet of immune heterogeneity in sepsis through the identification of a validated, four-gene apoptotic signature in classical monocytes. Beyond its diagnostic utility, this signature serves as a molecular indicator of immune state, enabling refined patient stratification. These findings lay the groundwork for precision immunopharmacology, where apoptosis-targeted or anti-inflammatory therapies can be tailored to individual immune profiles.
