# Tissue-invasive CMV disease is associated with poor prognosis during remission induction therapy for autoimmune inflammatory rheumatic diseases

**Authors:** Hideki Oka, Shuji Sumitomo, Chisato Miyakoshi, Koichiro Ohmura

PMC · DOI: 10.3389/fimmu.2026.1696516 · Frontiers in Immunology · 2026-02-12

## TL;DR

Tissue-invasive CMV disease during treatment for autoimmune rheumatic diseases is linked to worse outcomes, including higher mortality and more infections.

## Contribution

The study distinguishes between CMV infection and tissue-invasive CMV disease in autoimmune patients, revealing distinct clinical outcomes.

## Key findings

- CMV disease is associated with higher antigenemia, more coincident infections, and higher mortality.
- Kaplan–Meier analysis shows poorer survival in patients with CMV disease.
- Antigen count (cutoff: 36) is the best predictor of CMV disease.

## Abstract

Cytomegalovirus (CMV) is a notable health concern in immunocompromised individuals and presents as CMV reactivation (CMV infection) or CMV reactivation with tissue invasion (CMV disease). However, few studies have distinguished these CMV patterns during induction therapy for autoimmune inflammatory rheumatic diseases (AIIRDs). This study investigated the clinical characteristics of patients with CMV disease, diagnosed through histopathology, immunohistochemistry, or polymerase chain reaction, during induction therapy for AIIRDs in comparison with those of patients with CMV infection.

This single-center retrospective study included patients with AIIRDs undergoing remission induction therapy with glucocorticoids ≥20 mg/day for ≥4 weeks, hospitalized between 2013 and 2024. Data on clinical characteristics, treatments, and outcomes were collected, and CMV disease, determined by histopathological findings, was compared with CMV infection.

Among 82 patients administered AIIRDs and positive for CMV antigenemia, 14 had CMV disease and 68 had CMV infection. CMV disease was associated with lower platelet counts, higher aspartate aminotransferase/alanine transaminase levels, and higher maximum antigenemia. The prevalence of coincident infections (93% vs. 32%) and mortality rate (57% vs. 24%) were higher in patients with CMV disease. Kaplan–Meier analysis showed poorer survival for patients with CMV disease (log-rank test, p=0.027). Receiver operating characteristic analysis identified antigen count (cutoff: 36) as the best predictor of CMV disease.

CMV disease during remission induction therapy for AIIRDs is associated with higher antigenemia, more coincident infections, and poorer survival compared with CMV infection. Identifying the risk factors for CMV disease, including antigenemia and coincident infections, can improve patient outcomes.

## Linked entities

- **Diseases:** CMV infection (MONDO:0005132)

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** CMV antigenemia (MESH:D003586), mucosal lesions (MESH:D009059), CMV pneumonitis (MESH:D011014), hypoalbuminemia (MESH:D034141), fatigue (MESH:D005221), fever (MESH:D005334), dermatomyositis (MESH:D003882), polyarteritis nodosa (MESH:D010488), CMV reactivation (MESH:D000085343), SLE (MESH:D008180), CMV retinitis (MESH:D017726), Inflammatory (MESH:D007249), gastrointestinal symptoms (MESH:D012817), immunoglobulin A vasculitis (MESH:D014657), Takayasu arteritis (MESH:D013625), opportunistic infections (MESH:D009894), anti-neutrophil cytoplasmic antibody-associated vasculitis (MESH:D056648), AIIRDs (MESH:D012213), DM (MESH:D009223), organ damage (MESH:D000092124), oral candidiasis (MESH:D002180), liver dysfunction (MESH:D017093), Candida infections (MESH:D002177), hepatocellular injury (MESH:D056486), infectious disease (MESH:D003141), sepsis (MESH:D018805), eosinophilic granulomatosis with polyangiitis (MESH:D014890), giant cell arteritis (MESH:D013700), Mortality (MESH:D003643), cytopenia (MESH:D006402), Still's disease (MESH:D016706), bacteremia (MESH:D016470), Gastrointestinal CMV disease (MESH:D005767), Infections (MESH:D007239), Ag (MESH:D019588), rheumatic diseases (MESH:D012216), ulcers (MESH:D014456), polymyositis (MESH:D017285)
- **Chemicals:** MTX (MESH:D008727), cyclophosphamide (MESH:D003520), RTX (MESH:C024353), MMF (MESH:D009173), foscarnet (MESH:D017245), Ganciclovir (MESH:D015774), AZA (MESH:D001379), steroid (MESH:D013256), Creatinine (MESH:D003404), AIIRDs (-), rituximab (MESH:D000069283)
- **Species:** Cytomegalovirus (genus) [taxon 10358], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC12935964/full.md

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Source: https://tomesphere.com/paper/PMC12935964