Key result
Higher Th1/Treg ratio linked to ~4-fold greater AF risk, indicating an adaptive immune shift.
Why the study?
Atrial fibrillation involves adaptive immune imbalance within T-cell subsets, but systematic profiles in Asian cohorts remain limited.
Is atrial fibrillation associated with peripheral adaptive immune dysregulation (Th1/Th17-Treg imbalance) in Asian patients?
Case-Control (n=260)
Is atrial fibrillation associated with peripheral adaptive immune dysregulation (Th1/Th17-Treg imbalance) in Asian patients?
Odds Ratio: 4.2 (95% CI 1.72–10.24)
p-value: p=0.002
Atrial fibrillation in Asian patients is associated with an adaptive immune shift toward Th1/Th17 relative to Treg cells, suggesting a role for immune dysregulation in AF pathogenesis.
Supports immune dysregulation in Asian AF; hypothesis-generating and requires prospective validation before clinical consideration.
BACKGROUND: Atrial fibrillation (AF) involves adaptive immune imbalance, particularly within T-cell subsets, yet systematic profiles in Asian cohorts remain limited. OBJECTIVES: The authors aimed to characterize peripheral adaptive immune dysregulation in Asian patients with AF and to examine heterogeneity across AF subtypes and demographics. METHODS: In this case-control study of 173 AF patients and 87 controls, cases were adults with electrocardiogram-confirmed AF recruited from the hospital; controls were participants undergoing routine examinations who were in sinus rhythm and had no structural heart disease. T-cell subsets were quantified by flow cytometry and serum cytokines by enzyme-linked immunosorbent assay. Multivariable logistic models, adjusted for left atrial diameter, left ventricular ejection fraction, and neutrophil-to-lymphocyte ratio, assessed associations of immune indices with AF. RESULTS: AF was characterized by higher T helper (Th)1 and Th17 cell counts and percentages, with no significant difference in T regulatory cells (Tregs); accordingly, Th1/Treg and Th17/Treg ratios were higher (all P < 0.05). Systemic inflammatory markers (high-sensitivity C-reactive protein, interleukin-6) and effector cytokines (interferon-γ, interleukin-17A) were elevated in AF. In multivariable models, higher Th17 count (OR: 3.30; 95% CI: 1.27-8.53; P = 0.014) and Th1/Treg (OR: 4.20; 95% CI: 1.72-10.24; P = 0.002) were associated with AF. Immune alterations appeared broader in paroxysmal AF, whereas persistent AF showed a more selective Th1/Treg imbalance. Patterns were generally consistent across age, sex, and body mass index strata in exploratory analyses. CONCLUSIONS: In this Asian cohort, AF was associated with an adaptive immune shift toward Th1/Th17 relative to Treg, with subtype-specific patterns. These associations are hypothesis-generating and warrant prospective, tissue-level studies to clarify mechanisms and clinical relevance.
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Liu et al. (2026) conducted a case-control in Atrial fibrillation (n=260). Higher Th1/Treg ratio vs. Controls in sinus rhythm was evaluated on Atrial fibrillation (OR 4.20, 95% CI 1.72-10.24, p=0.002). A higher Th1/Treg ratio was significantly associated with atrial fibrillation (OR 4.20; 95% CI 1.72-10.24; P=0.002), indicating an adaptive immune shift in this Asian cohort.
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