Proteomic profiling of neutrophils and plasma in community-acquired pneumonia reveals crucial proteins in diverse biological pathways linked to clinical outcome

Front Immunol. 2024 Oct 18:15:1470383. doi: 10.3389/fimmu.2024.1470383. eCollection 2024.

Abstract

Introduction: Neutrophils play a dichotomous role in community-acquired pneumonia (CAP), providing protection and potentially causing damage. Existing research on neutrophil function in CAP relies on animal studies, leaving a gap in patient-centered investigations.

Methods: We used mass spectrometry to characterize the neutrophil proteome of moderately ill CAP patients at general ward admission and related the proteome to controls and clinical outcomes.

Results: We prospectively included 57 CAP patients and 26 controls and quantified 3482 proteins in neutrophil lysates and 386 proteins in concurrently collected plasma. The extensively studied granule-related proteins in animal models did not drive the neutrophil proteome changes associated with human CAP. Proteome alterations were primarily characterized by an increased abundance of proteins related to (aerobic) metabolic activity and (m)RNA translation/processing, concurrent with a diminished presence of cytoskeletal organization-related proteins (all pathways p<0.001). Higher and lower abundances of specific proteins, primarily constituents of these pathways, were associated with prolonged time to clinical stability in CAP. Moreover, we identified a pronounced presence of platelet-related proteins in neutrophil lysates of particularly viral CAP patients, suggesting the existence of neutrophil-platelet complexes in non-critically ill CAP patients. Of the proteins measured in neutrophils, 4.3% were detected in plasma.

Discussion: Our study presents new perspectives on the neutrophil proteome associated with CAP, laying the groundwork for forthcoming patient-centred investigations. Our results could pave the way for targeted strategies to fine-tune neutrophil responses, potentially improving CAP outcomes.

Keywords: community-acquired pneumonia; general ward; innate immunity; mass spectrometry; neutrophil; pneumonia; proteomics.

MeSH terms

  • Aged
  • Community-Acquired Infections* / blood
  • Community-Acquired Infections* / immunology
  • Female
  • Humans
  • Male
  • Middle Aged
  • Neutrophils* / immunology
  • Neutrophils* / metabolism
  • Pneumonia* / blood
  • Pneumonia* / immunology
  • Pneumonia* / metabolism
  • Prospective Studies
  • Proteome*
  • Proteomics* / methods

Substances

  • Proteome

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. EM and JD received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No 847786 (FAIR). OC was supported by the Landsteiner Foundation (LSBR # 1901). AH and MV were supported by Landsteiner Foundation for Blood Transfusion Research grant LSBR # 1923. WW was supported by the Talud Foundation (Stichting Talud) for the Amsterdam UMC Corona Research Fund, the Netherlands Organisation for Health Research and Development (ZonMw; TURN-COVID grant number 10430142110001). The funders of this study had no role in study design, data collection, data analysis, data interpretation, or writing of the report.