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Updated: Jan 29, 2026

Detection of Anti-MDA5 Autoantibodies Using HeLa Cells and Immunocytochemistry with Light Microscopy
Published on: October 31, 2025
Anti-MDA5 antibody-positive rapidly progressive interstitial pneumonia without cutaneous manifestations
Junichi Aoyama1, Hiroki Hayashi1, Chika Yajima1
1Department of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Japan.
Abstract:
A 47-year-old man was referred to our hospital with a 1-month history of fever and dyspnea after inhalation of insecticide in a confined space. We diagnosed rapidly progressive interstitial pneumonia. High-dose methylprednisolone, tacrolimus, and intermittent infusion of cyclophosphamide were administered. His condition rapidly deteriorated; therefore, extracorporeal membrane oxygenation therapy was performed. Unfortunately, he died 69 days after admission. Although typical skin findings suggestive of dermatomyositis were absent, anti-melanoma differentiation-associate gene (anti-MDA5) antibody was positive. Our findings suggest that in patients with hyperferritinemia and rapidly progressive interstitial lung disease (RP-ILD) demonstrating random ground glass shadows and peripheral consolidations by high-resolution computed tomography (HRCT) even if skin manifestations related to dermatomyositis are not complicated, we should assume anti-MDA5 antibody-positive interstitial pneumonia.
Insights
This case study highlights anti-melanoma differentiation-associate gene (anti-MDA5) antibody-positive interstitial pneumonia. Early detection is crucial, even without typical skin symptoms, in patients with rapidly progressive interstitial lung disease (RP-ILD) and high ferritin.
Area of Science:
- Pulmonology
- Rheumatology
- Immunology
Background:
- Rapidly progressive interstitial lung disease (RP-ILD) presents a diagnostic challenge.
- Dermatomyositis-associated interstitial pneumonia often involves characteristic skin findings.
- Anti-melanoma differentiation-associate gene (anti-MDA5) antibody is increasingly recognized in ILD, sometimes without skin manifestations.
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