Dupilumab as an adjunct treatment for a patient with steroid-dependent immunoglobulin G4-related disease complicated by asthma: a case report

Abstract Introduction: Immunoglobulin G4-related disease (IgG4-RD) responds well to glucocorticoids but is often associated with relapses. Interleukin (IL)-4 and IL-13 are involved in the pathogenesis of IgG4-RD. We present the first case in which dupilumab was an effective adjunct treatment for a patient with steroid-dependent IgG4-RD complicated by asthma.Case study: A 57-year-old man was referred to our hospital for further investigation and treatment of proptosis with neck swelling in 2019. He developed a cough and swelling of the neck in 2016. He was diagnosed with asthma in 2017 and started receiving inhaled glucocorticoids and a long-acting beta-agonist. The patient started receiving oral prednisolone at a dose of 20 mg/day. Oral prednisolone reduced his symptoms, but he relapsed when treatment was tapered to less than 10 mg/day. He was diagnosed with IgG4-RD through a parotid gland biopsy.Results: Azathioprine was given to reduce systemic glucocorticoids. The prednisolone dose was gradually tapered to 10 mg/day, resulting in the relapse of proptosis and an asthma attack. We added dupilumab, and his asthma symptoms and proptosis improved. Serum IgG4 levels continued to decrease, and the prednisolone dose was tapered to 2 mg.Conclusion: Dupilumab might be useful as an adjunctive treatment for patients with steroid-dependent IgG4-RD complicated by asthma. Serum IgG4 levels can be used as a marker to monitor dupilumab treatment in IgG4-RD.

[1]  T. Mustelin,et al.  Allergic Aspects of IgG4-Related Disease: Implications for Pathogenesis and Therapy , 2021, Frontiers in Immunology.

[2]  Simona Baghai Sain,et al.  B lymphocytes directly contribute to tissue fibrosis in IgG4-Related Disease. , 2020, The Journal of allergy and clinical immunology.

[3]  Jason K. Lee,et al.  Response to: ‘Dupilumab as a potential steroid-sparing treatment for IgG4-related disease’ by Della-Torre et al , 2020, Annals of the Rheumatic Diseases.

[4]  F. Vély,et al.  Correspondence on: ‘Dupilumab as a novel steroid-sparing treatment for IgG4-related disease’ by Simpson et al , 2020, Annals of the Rheumatic Diseases.

[5]  M. Lanzillotta,et al.  Dupilumab as a potential steroid-sparing treatment for IgG4-related disease , 2020, Annals of the Rheumatic Diseases.

[6]  Jason K. Lee,et al.  Dupilumab as a novel steroid-sparing treatment for IgG4-related disease , 2019, Annals of the rheumatic diseases.

[7]  X. Zhang,et al.  Clinical outcomes and predictive relapse factors of IgG4‐related disease following treatment: a long‐term cohort study , 2019, Journal of internal medicine.

[8]  T. Takeuchi,et al.  Interleukin‐4 contributes to the shift of balance of IgG subclasses toward IgG4 in IgG4‐related disease , 2018, Cytokine.

[9]  P. Lipsky,et al.  Aberrant Expansion and Function of Follicular Helper T Cell Subsets in IgG4‐Related Disease , 2018, Arthritis & rheumatology.

[10]  Huadan Xue,et al.  Efficacy and safety of low dose Mycophenolate mofetil treatment for immunoglobulin G4-related disease: a randomized clinical trial , 2018, Rheumatology.

[11]  J. Stone,et al.  IgG4-related disease , 2017, Current opinion in rheumatology.

[12]  F. Maurier,et al.  T Cell Polarization toward TH2/TFH2 and TH17/TFH17 in Patients with IgG4-Related Disease , 2017, Front. Immunol..

[13]  Jefte M. Drijvers,et al.  Clonal expansion of CD4(+) cytotoxic T lymphocytes in patients with IgG4-related disease. , 2016, The Journal of allergy and clinical immunology.

[14]  P. Klenerman,et al.  Elevated Serum IgG4 Levels in Diagnosis, Treatment Response, Organ Involvement, and Relapse in a Prospective IgG4-Related Disease UK Cohort , 2016, The American Journal of Gastroenterology.

[15]  K. Takata,et al.  Interleukin 13-positive mast cells are increased in immunoglobulin G4-related sialadenitis , 2015, Scientific Reports.

[16]  S. Kawa,et al.  Autoimmune pancreatitis can develop into chronic pancreatitis , 2014, Orphanet Journal of Rare Diseases.

[17]  J. Stone,et al.  Prevalence of atopy, eosinophilia, and IgE elevation in IgG4‐related disease , 2014, Allergy.

[18]  Wei-Chih Liao,et al.  Long-term outcomes of autoimmune pancreatitis: a multicentre, international analysis , 2012, Gut.

[19]  S. Toda,et al.  Periostin promotes chronic allergic inflammation in response to Th2 cytokines. , 2012, The Journal of clinical investigation.

[20]  T. Hibi,et al.  Comprehensive diagnostic criteria for IgG4-related disease (IgG4-RD), 2011 , 2012, Modern rheumatology.

[21]  Y. Nakanuma,et al.  IgG4-Related Disease: A Cross-sectional Study of 114 Cases , 2010, The American journal of surgical pathology.

[22]  B. Petersen,et al.  Differences in clinical profile and relapse rate of type 1 versus type 2 autoimmune pancreatitis. , 2010, Gastroenterology.

[23]  M. Deheragoda,et al.  Presentation and management of post-treatment relapse in autoimmune pancreatitis/immunoglobulin G4-associated cholangitis. , 2009, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

[24]  T. Shimosegawa,et al.  Standard steroid treatment for autoimmune pancreatitis , 2009, Gut.

[25]  J. K. Lee,et al.  Review of 67 Patients With Autoimmune Pancreatitis in Korea: A Multicenter Nationwide Study , 2008, Pancreas.

[26]  J. Murray,et al.  Autoimmune pancreatitis, Part II: the relapse. , 2008, Gastroenterology.

[27]  Y. Nakanuma,et al.  Th2 and regulatory immune reactions are increased in immunoglobin G4‐related sclerosing pancreatitis and cholangitis , 2007, Hepatology.

[28]  J D Malley,et al.  Studies of murine schistosomiasis reveal interleukin‐13 blockade as a treatment for established and progressive liver fibrosis , 2001, Hepatology.

[29]  T. Sumida,et al.  Preferential M2 macrophages contribute to fibrosis in IgG4-related dacryoadenitis and sialoadenitis, so-called Mikulicz's disease. , 2015, Clinical immunology.

[30]  K. Okazaki,et al.  Comprehensive Diagnostic Criteria for IgG4-Related Disease , 2014 .