Interferon-induced interstitial lung disease: a rare adverse effect induced by pegylated interferon-alpha in a patient with chronic hepatitis B-case report

BACKGROUND: Interferon (IFN)-induced interstitial lung disease (ILD) is a rare but potentially fatal complication. While predominantly reported in patients with chronic hepatitis C, its occurrence during therapy for chronic hepatitis B is exceedingly rare. Although steroids are widely used empirically, the optimal therapeutic regimen remains to be elucidated. CASE PRESENTATION: We reported a case of a middle-aged, non-smoking Asian female patient with chronic hepatitis B who received weekly subcutaneous injection of pegylated interferon-alpha (Peg-IFNα) (alternating 135 μg or 180 μg). One month after treatment initiation (following the fifth dose), she developed exertional dyspnea, dry cough, and a low-grade fever. High-resolution computed tomography revealed bilateral interlobular septal thickening with subpleural ground-glass opacities. Pulmonary function tests demonstrated a reduced diffusion capacity, however, uncommon in ILD, the patient also exhibited pulmonary hyperinflation. Serological tests did not reveal any abnormalities in white blood cell count, C-reactive protein, procalcitonin, autoantibodies, or anti-respiratory virus antibodies. Echocardiography confirmed structurally normal cardiac chambers and preserved left ventricular systolic function (ejection fraction of 71%). After excluding infectious, autoimmune, and cardiogenic causes, the IFN-induced ILD was diagnosed. After discontinuation of Peg-IFNα and initiation of methylprednisolone therapy, the patient's respiratory symptoms improved markedly within 24 h and resolved completely within a week. During follow ups, no respiratory symptom reoccurred, and chest imaging and the pulmonary function resolved gradually. CONCLUSION: In this study, we reported a female case who developed an IFN-induced ILD while monotherapy with IFN for chronic hepatitis B, and who experienced rapid clinical improvement after initiation of steroid therapy. To our knowledge, IFN-induced ILD is exceedingly rare in the context of PEG-IFNα monotherapy for chronic hepatitis B, particularly in female patients. Clinicians should maintain a high index of suspicion for IFN-induced ILD when unexplained pulmonary symptoms arise during therapy. Early recognition and appropriate steroid administration appear to be effective strategies for managing disease progression.

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Journal
BMC Pulmonary Medicine
Published
2026-06-19
DOI
https://doi.org/10.1186/s12890-026-04426-5
Primary Topic
Hepatitis C virus research
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article
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article

Interferon-induced interstitial lung disease: a rare adverse effect induced by pegylated interferon-alpha in a patient with chronic hepatitis B-case report

Yuxing Wang, Shuangshuang Zhang, Haoyue Yu, Yu Zhou et al.
BMC Pulmonary Medicine
Hepatitis C virus research
article

Interferon-induced interstitial lung disease: a rare adverse effect induced by pegylated interferon-alpha in a patient with chronic hepatitis B-case report

Yuxing Wang, Shuangshuang Zhang, Haoyue Yu, Yu Zhou, Xuemei Yang, Qingqing Wen
article en

Abstract

BACKGROUND: Interferon (IFN)-induced interstitial lung disease (ILD) is a rare but potentially fatal complication. While predominantly reported in patients with chronic hepatitis C, its occurrence during therapy for chronic hepatitis B is exceedingly rare. Although steroids are widely used empirically, the optimal therapeutic regimen remains to be elucidated. CASE PRESENTATION: We reported a case of a middle-aged, non-smoking Asian female patient with chronic hepatitis B who received weekly subcutaneous injection of pegylated interferon-alpha (Peg-IFNα) (alternating 135 μg or 180 μg). One month after treatment initiation (following the fifth dose), she developed exertional dyspnea, dry cough, and a low-grade fever. High-resolution computed tomography revealed bilateral interlobular septal thickening with subpleural ground-glass opacities. Pulmonary function tests demonstrated a reduced diffusion capacity, however, uncommon in ILD, the patient also exhibited pulmonary hyperinflation. Serological tests did not reveal any abnormalities in white blood cell count, C-reactive protein, procalcitonin, autoantibodies, or anti-respiratory virus antibodies. Echocardiography confirmed structurally normal cardiac chambers and preserved left ventricular systolic function (ejection fraction of 71%). After excluding infectious, autoimmune, and cardiogenic causes, the IFN-induced ILD was diagnosed. After discontinuation of Peg-IFNα and initiation of methylprednisolone therapy, the patient's respiratory symptoms improved markedly within 24 h and resolved completely within a week. During follow ups, no respiratory symptom reoccurred, and chest imaging and the pulmonary function resolved gradually. CONCLUSION: In this study, we reported a female case who developed an IFN-induced ILD while monotherapy with IFN for chronic hepatitis B, and who experienced rapid clinical improvement after initiation of steroid therapy. To our knowledge, IFN-induced ILD is exceedingly rare in the context of PEG-IFNα monotherapy for chronic hepatitis B, particularly in female patients. Clinicians should maintain a high index of suspicion for IFN-induced ILD when unexplained pulmonary symptoms arise during therapy. Early recognition and appropriate steroid administration appear to be effective strategies for managing disease progression.

BMC Pulmonary Medicine
Army Medical University (CN), Daping Hospital (CN), The 309th Hospital of Chinese People's Liberation Army (CN)
Good health and well-being
Openalex Percentile: Top 8%
Hepatitis C virus research
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