# Peripheral blood T-cell subsets combined with EGRIS score predict the need for mechanical ventilation in Guillain–Barré syndrome

**Authors:** Feihong Jia, Xinrui Wang, Yuan Chen, Yunshu Li, Xinshu Du, Hongping Chen, Di Zhong

PMC · DOI: 10.3389/fimmu.2026.1747416 · Frontiers in Immunology · 2026-02-04

## TL;DR

This study shows that specific blood T-cell levels and the EGRIS score can help predict if GBS patients will need mechanical ventilation.

## Contribution

The study introduces a novel combination of T-cell subsets and the EGRIS score to predict mechanical ventilation needs in GBS.

## Key findings

- CD8+ and NK cell counts moderately distinguish GBS patients from healthy controls.
- Higher CD4+ T cell counts are linked to reduced need for mechanical ventilation in GBS.
- Combining CD8+ T, CD4+ T cells, and EGRIS score improves prediction of mechanical ventilation needs.

## Abstract

The pathogenesis of Guillain–Barré syndrome (GBS) may involve lymphocyte-mediated immune mechanisms. This study aimed to investigate the relationship between peripheral blood lymphocyte subsets and disease onset, severity, and the need for mechanical ventilation in patients with GBS.

This cohort study included 55 patients with GBS and 58 healthy controls. The association between peripheral blood lymphocyte subsets and the onset and severity of GBS was investigated. Among the GBS patients, 26 were classified into a non-mechanical ventilation group and 29 into a mechanical ventilation group, and the predictive value of peripheral blood lymphocyte subsets for mechanical ventilation was evaluated. Furthermore, the study examined the expression of relevant lymphocyte subsets in the sciatic nerve of experimental autoimmune neuritis (EAN) rat models at different disease stages.

ROC curve analysis showed that both CD8+ T cell counts and NK cell counts had moderate discriminative ability in distinguishing patients with GBS from controls. The AUC for CD8+ T cell counts was 0.73 (95% CI: 0.637–0.836), with an optimal cutoff value of 394.39 cells/μL, while the AUC for NK cell counts was 0.81 (95% CI: 0.731–0.893), with an optimal cutoff value of 147.7 cells/μL. Total lymphocyte counts, total T cell counts, CD8+ T cell counts, and CD4+ T cell counts were negatively correlated with Hughes peak score (all P ≤ 0.005). Logistic regression showed that higher peripheral CD4+ T cell counts was associated with reduced need for mechanical ventilation (OR = 0.997; 95% CI: 0.994–1.000, P = 0.032). The combined ROC analysis of CD8+ T cell counts, CD4+ T cell counts, and the EGRIS score demonstrated good discriminative ability for identifying GBS patients who required mechanical ventilation, with an AUC of 0.87 (95% CI, 0.772–0.971, P < 0.001). In the EAN model, CD4+ T cell expression was increased in sciatic nerve tissue.

Peripheral blood lymphocyte subsets show potential value in differentiating disease severity and the need for mechanical ventilation in patients with GBS, highlighting the clinical significance of immune cell profiling in risk stratification.

## Linked entities

- **Diseases:** Guillain–Barré syndrome (MONDO:0016218)
- **Species:** Homo sapiens (taxon 9606), Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Rac2 (Rac family small GTPase 2) [NCBI Gene 19354], PMP22 (peripheral myelin protein 22) [NCBI Gene 5376] {aka CIDP, CMT1A, CMT1E, DSS, GAS-3, GAS3}, KLRC2 (killer cell lectin like receptor C2) [NCBI Gene 3822] {aka CD159c, NKG2-C, NKG2C}, Cd4 (Cd4 molecule) [NCBI Gene 24932] {aka W3/25, p55}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, Plcg2 (phospholipase C, gamma 2) [NCBI Gene 234779] {aka PLC-gamma-2, PLCgamma2, Plcg-2}
- **Diseases:** systemic lupus erythematosus (MESH:D008180), autonomic dysfunction (MESH:D001342), juvenile dermatomyositis (MESH:D003882), cranial nerve palsy (MESH:D003389), paraneoplastic neuropathy (MESH:D020364), paralysis (MESH:D010243), MFS (MESH:D008382), immune-mediated neuropathies (MESH:C567355), EAN (MESH:D009444), diarrhea (MESH:D003967), Erasmus GBS Respiratory Insufficiency (MESH:D012131), cytomegalovirus (MESH:D003586), neurological diseases (MESH:D020271), autoimmune disorders (MESH:D001327), neuroinflammation (MESH:D000090862), dyspnea (MESH:D004417), AIDP (MESH:D020275), Sjogren's syndrome (MESH:D012859), miller fisher syndrome (MESH:D019846), weakness (MESH:D018908), sensory disturbances (MESH:D012678), diabetes (MESH:D003920), peripheral nerve injury (MESH:D059348), inflammation (MESH:D007249), CIDP (MESH:D020277), neuroimmunology diseases (MESH:D004194), respiratory tract infection (MESH:D012141), axonal injury (MESH:D001480), alopecia areata (MESH:D000506), neuropathy (MESH:D009422), multiple sclerosis (MESH:D009103), autoimmune-mediated peripheral neuropathy (MESH:D010523), type 1 diabetes (MESH:D003922), axonal degeneration (MESH:D009410), areflexia (MESH:D000071699), sciatic nerve demyelination (MESH:D020426), cytotoxicity (MESH:D064420), infections (MESH:D007239), COVID-19 (MESH:D000086382), neurological injury (MESH:D020196), demyelinating polyneuropathy (MESH:D003711), bacterial and viral infections (MESH:D014777), heavy metal poisoning (MESH:D000075322), rheumatoid arthritis (MESH:D001172)
- **Chemicals:** cholesterol (MESH:D002784), Triton X-100 (MESH:D017830), sodium pentobarbital (MESH:D010424), FITC (MESH:D016650), OCT (MESH:C051883), DAPI (MESH:C007293), ice (MESH:D007053), PBS (MESH:D007854), incomplete Freund's adjuvant (MESH:C114843), paraformaldehyde (MESH:C003043), lipid (MESH:D008055), amino acids (MESH:D000596)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Mycoplasmoides pneumoniae (Filterable agent of primary atypical pneumonia, species) [taxon 2104], Mus musculus (house mouse, species) [taxon 10090], Zika virus (no rank) [taxon 64320], Mycobacterium tuberculosis H37Ra (strain) [taxon 419947], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376], Mycobacterium tuberculosis (species) [taxon 1773]

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913372/full.md

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Source: https://tomesphere.com/paper/PMC12913372