# Neutrophil CD64 index for rapid diagnosis of Pneumocystis jirovecii pneumonia in malignancy patients requiring mechanical ventilation: a retrospective analysis

**Authors:** Xiaoming Li, Hongyu Yi, Guixin Wu, Aiting He, Rui Li, Yi Long, Changhai Lin, Zhengying Jiang

PMC · DOI: 10.3389/fmicb.2026.1706786 · Frontiers in Microbiology · 2026-01-27

## TL;DR

The neutrophil CD64 index is a promising non-invasive tool for quickly diagnosing Pneumocystis jirovecii pneumonia and predicting mortality in cancer patients on ventilators.

## Contribution

The study introduces the neutrophil CD64 index as a dual-purpose biomarker for rapid PJP diagnosis and mortality prediction in ventilated malignancy patients.

## Key findings

- The nCD64 index was significantly higher in PJP patients compared to non-PJP patients.
- The nCD64 index showed high sensitivity and specificity for PJP diagnosis with an AUC of 0.846.
- Post-therapy nCD64 index elevation predicted 28-day mortality with high accuracy.

## Abstract

Pneumocystis jirovecii pneumonia (PJP) incidence and associated mortality have risen significantly in non-HIV immunocompromised patients, highlighting the urgent need for rapid, non-invasive diagnostics. Current methods face limitations including invasiveness, prolonged processing, or inadequate specificity. The neutrophil CD64 (nCD64) index emerges as a promising novel biomarker. Here, we conducted this study to evaluate the diagnostic performance of nCD64 index for PJP and further assess the predictive value of its longitudinal changes for 28-day mortality.

This retrospective cohort study (July 2022–March 2025) analyzed mechanically ventilated malignancy patients with unexplained diffuse pulmonary infiltrates at a tertiary intensive care unit (ICU). PJP diagnosis required predefined clinical, radiological, and bronchoalveolar lavage fluid metagenomic next-generation sequencing (BALF mNGS) criteria. The nCD64 index was measured via flow cytometry at ICU admission and serially after ≥3 days of anti-PJP therapy. Diagnostic performance for PJP and prognostic value for 28-day mortality were assessed.

Among 28 PJP and 38 non-PJP patients, nCD64 index was significantly higher in PJP (13.33 vs. 2.84, p < 0.001). Receiver operating characteristic (ROC) curve analysis showed an area under the curve (AUC) of 0.846 (95% CI: 0.736–0.932) for PJP diagnosis, with sensitivity 89.3% and specificity 71.1% at cutoff ≥7. Multivariate analysis confirmed nCD64 index as an independent PJP predictor (OR = 1.097, 95% CI: 1.026–1.173; p = 0.007). Post-therapy nCD64 index elevation predicted 28-day mortality with high sensitivity (81.8%) and specificity (86.7%).

The nCD64 index functions as a dual-purpose biomarker for malignancy patients with respiratory failure requiring mechanical ventilation: it provides a rapid, non-invasive diagnostic tool for PJP and dynamically stratifies mortality risk. Moreover, dynamic tracking offers a real-time window into treatment response, guiding therapeutic decisions.

## Linked entities

- **Diseases:** Pneumocystis jirovecii pneumonia (MONDO:0019121), malignancy (MONDO:0004992)

## Full-text entities

- **Genes:** FCGR1A (Fc gamma receptor Ia) [NCBI Gene 2209] {aka CD64, CD64A, FCG1, FCGR1, FCRI, FcgammaRI}
- **Diseases:** malignancy (MESH:D009369), respiratory failure (MESH:D012131), PJP (MESH:D011020), pulmonary infiltrates (MESH:D017254)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12886426/full.md

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Source: https://tomesphere.com/paper/PMC12886426