# Serum interferon-λ3 as a short-term biomarker of disease control in anti-MDA5-positive dermatomyositis-associated ILD

**Authors:** Yoshihiro Kitahara, Tomoyuki Fujisawa, Atsuki Fukada, Keigo Koda, Taisuke Akamatsu, Masaki Ikeda, Masato Fujii, Mitsuru Niwa, Yusuke Kaida, Hiroyuki Matsuda, Koshi Yokomura, Naoki Koshimizu, Mikio Toyoshima, Shiro Imokawa, Dai Hashimoto, Keita Yamashita, Moriya Iwaizumi, Masato Maekawa, Yusuke Inoue, Hideki Yasui, Hironao Hozumi, Yuzo Suzuki, Masato Karayama, Kazuki Furuhashi, Noriyuki Enomoto, Naoki Inui, Takafumi Suda

PMC · DOI: 10.1038/s41598-026-37104-x · Scientific Reports · 2026-01-24

## TL;DR

This study shows that serum IFN-λ3 levels can help track treatment response in a specific type of lung disease linked to a skin condition.

## Contribution

The study introduces serum IFN-λ3 as a potential short-term biomarker for disease control in anti-MDA5-positive DM-ILD.

## Key findings

- IFN-λ3 levels dropped significantly in patients with good disease control after treatment.
- Poor control patients showed no significant change in IFN-λ3 levels.
- Early IFN-λ3 levels predicted long-term outcomes in these patients.

## Abstract

This study aimed to assess the clinical utility of serum interferon-lambda 3 (IFN-λ3) as a sequential biomarker for treatment response and disease control in patients with anti-melanoma differentiation-associated gene 5 (MDA5) antibody-positive dermatomyositis (DM)-associated interstitial lung disease (ILD). Serum IFN-λ3 levels were measured in 24 patients with anti-MDA5 antibody-positive DM-ILD at diagnosis and 1 month after initiating immunosuppressive therapy. Patients were categorized into two groups based on clinical outcomes: a good control group (n = 16; survived without relapse for ≥ 1 year) and a poor control group (n = 8; died from ILD progression or relapse within 1 year). Changes in serum IFN-λ3 levels and differences between groups were analyzed. In the good control group, serum IFN-λ3 levels significantly decreased from 94.6 to 12.7 pg/mL (p < 0.001), whereas no significant change was observed in the poor control group (129.0 to 118.8 pg/mL). Furthermore, serum IFN-λ3 levels at 1 month were significantly lower in the good control group than in the poor control group (p = 0.004). Serum IFN-λ3 levels may reflect short-term treatment response and could serve as a useful sequential biomarker for assessing disease control in patients with anti-MDA5 antibody-positive DM-ILD.

The online version contains supplementary material available at 10.1038/s41598-026-37104-x.

## Linked entities

- **Genes:** IFIH1 (interferon induced with helicase C domain 1) [NCBI Gene 64135]
- **Diseases:** dermatomyositis (MONDO:0016367), interstitial lung disease (MONDO:0015925)

## Full-text entities

- **Genes:** IFNL3 (interferon lambda 3) [NCBI Gene 282617] {aka IFN-lambda-3, IFN-lambda-4, IL-28B, IL-28C, IL28B, IL28C}, IFIH1 (interferon induced with helicase C domain 1) [NCBI Gene 64135] {aka AGS7, Hlcd, IDDM19, IMD95, MDA-5, MDA5}
- **Diseases:** DM-ILD (MESH:D017563), DM (MESH:D003882)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12901154/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12901154/full.md

---
Source: https://tomesphere.com/paper/PMC12901154