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Published in: American Journal of Clinical Dermatology 2/2024

Open Access 29-12-2023 | Bullous Pemphigoid | Review Article

Advancements in Bullous Pemphigoid Treatment: A Comprehensive Pipeline Update

Authors: Meropi Karakioulaki, Kilian Eyerich, Aikaterini Patsatsi

Published in: American Journal of Clinical Dermatology | Issue 2/2024

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Abastract

Bullous pemphigoid (BP) is a common autoimmune bullous disease affecting mainly the elderly, with rising incidence due to increased life expectancy. This disease is characterized by tense bullous lesions on normal or erythematous skin, accompanied by pruritus. BP pathogenesis involves autoantibodies against hemidesmosomal proteins BP180 and BP230, leading to detachment at the dermo-epidermal junction as well as blister formation. BP is associated with coexisting comorbidities and drug exposure, and its management often requires high doses or chronic use of systemic glucocorticoids, posing risks of adverse effects. This review focuses on novel treatment options for BP, exploring therapies targeting different immune pathways. Rituximab, a CD20 monoclonal antibody, depletes B-lymphocytes and has shown efficacy in severe cases. Dupilumab, targeting interleukin (IL)-4 receptor α and thus blocking IL-4 and IL-13, downregulates type 2 helper (Th2) responses and has demonstrated promising results. Targeting eosinophil-related molecules using bertilimumab and AKST4290 has yielded positive results in clinical trials. Omalizumab, an immunoglobulin (Ig) E antibody, can reduce disease severity and allows corticosteroid tapering in a number of cases. Complement inhibitors such as nomacopan and avdoralimab are being investigated. IL-17 and IL-23 inhibitors such as secukinumab and tildrakizumab have shown potential in a limited number of case reports. Neonatal Fc receptor antagonists such as efgartigimod are under investigation. Additionally, topical therapies and Janus kinase inhibitors are being explored as potential treatments for BP. These novel therapies offer promising alternatives for managing BP, with potential to improve outcomes and reduce high cumulative doses of systemic corticosteroids and related toxicities. Further research, including controlled clinical trials, is needed to establish their efficacy, safety, and optimal dosing regimens for BP management.
Literature
1.
go back to reference van Beek N, et al. IgE-mediated mechanisms in bullous pemphigoid and other autoimmune bullous diseases. Expert Rev Clin Immunol. 2016;12(3):267–77.PubMedCrossRef van Beek N, et al. IgE-mediated mechanisms in bullous pemphigoid and other autoimmune bullous diseases. Expert Rev Clin Immunol. 2016;12(3):267–77.PubMedCrossRef
4.
go back to reference Kridin K, Shihade W, Bergman R. Mortality in patients with bullous pemphigoid: a retrospective cohort study, systematic review and meta-analysis. Acta Derm Venereol. 2019;99(1):72–7.PubMed Kridin K, Shihade W, Bergman R. Mortality in patients with bullous pemphigoid: a retrospective cohort study, systematic review and meta-analysis. Acta Derm Venereol. 2019;99(1):72–7.PubMed
5.
go back to reference Kridin K, et al. Mortality in bullous pemphigoid: a systematic review and meta-analysis of standardized mortality ratios. J Dermatol. 2018;45(9):1094–100.PubMedCrossRef Kridin K, et al. Mortality in bullous pemphigoid: a systematic review and meta-analysis of standardized mortality ratios. J Dermatol. 2018;45(9):1094–100.PubMedCrossRef
8.
go back to reference Chai ZT, et al. Diabetes mellitus and hyperglycemic complications in bullous pemphigoid. J Am Acad Dermatol. 2020;82(5):1234–7.PubMedCrossRef Chai ZT, et al. Diabetes mellitus and hyperglycemic complications in bullous pemphigoid. J Am Acad Dermatol. 2020;82(5):1234–7.PubMedCrossRef
9.
go back to reference Kibsgaard L, et al. Increased frequency of multiple sclerosis among patients with bullous pemphigoid: a population-based cohort study on comorbidities anchored around the diagnosis of bullous pemphigoid. Br J Dermatol. 2017;176(6):1486–91.PubMedCrossRef Kibsgaard L, et al. Increased frequency of multiple sclerosis among patients with bullous pemphigoid: a population-based cohort study on comorbidities anchored around the diagnosis of bullous pemphigoid. Br J Dermatol. 2017;176(6):1486–91.PubMedCrossRef
10.
go back to reference Lee S, et al. Association of bullous pemphigoid and comorbid health conditions: a case-control study. Arch Dermatol Res. 2021;313(5):327–32.PubMedCrossRef Lee S, et al. Association of bullous pemphigoid and comorbid health conditions: a case-control study. Arch Dermatol Res. 2021;313(5):327–32.PubMedCrossRef
11.
go back to reference Baum, S., et al., Prevalence, Spectrum and Clinical Implications of Malignancies in Patients with Bullous Pemphigoid. Acta Derm Venereol, 2023. 103:adv00888. Baum, S., et al., Prevalence, Spectrum and Clinical Implications of Malignancies in Patients with Bullous Pemphigoid. Acta Derm Venereol, 2023. 103:adv00888.
12.
go back to reference Salemme A, et al. Gliptin-associated bullous pemphigoid shows peculiar features of anti-BP180 and -BP230 humoral response: Results of a multicenter study. J Am Acad Dermatol. 2022;87(1):56–63.PubMedCrossRef Salemme A, et al. Gliptin-associated bullous pemphigoid shows peculiar features of anti-BP180 and -BP230 humoral response: Results of a multicenter study. J Am Acad Dermatol. 2022;87(1):56–63.PubMedCrossRef
14.
go back to reference Afarideh M, Borucki R, Werth VP. A review of the immunologic pathways involved in bullous pemphigoid and novel therapeutic targets. J Clin Med. 2022;11(10):2856.PubMedPubMedCentralCrossRef Afarideh M, Borucki R, Werth VP. A review of the immunologic pathways involved in bullous pemphigoid and novel therapeutic targets. J Clin Med. 2022;11(10):2856.PubMedPubMedCentralCrossRef
15.
go back to reference Kasperkiewicz M, et al. COVID-19 pandemic and autoimmune bullous diseases: a cross-sectional study of the International Pemphigus and Pemphigoid Foundation. J Eur Acad Dermatol Venereol. 2021;35(7):e418–21.PubMedPubMedCentralCrossRef Kasperkiewicz M, et al. COVID-19 pandemic and autoimmune bullous diseases: a cross-sectional study of the International Pemphigus and Pemphigoid Foundation. J Eur Acad Dermatol Venereol. 2021;35(7):e418–21.PubMedPubMedCentralCrossRef
16.
go back to reference Maronese CA, et al. Bullous pemphigoid associated with COVID-19 vaccines: an Italian Multicentre Study. Front Med (Lausanne). 2022;9: 841506.PubMedCrossRef Maronese CA, et al. Bullous pemphigoid associated with COVID-19 vaccines: an Italian Multicentre Study. Front Med (Lausanne). 2022;9: 841506.PubMedCrossRef
17.
go back to reference Kasperkiewicz M, Zillikens D. The pathophysiology of bullous pemphigoid. Clin Rev Allergy Immunol. 2007;33(1–2):67–77.PubMedCrossRef Kasperkiewicz M, Zillikens D. The pathophysiology of bullous pemphigoid. Clin Rev Allergy Immunol. 2007;33(1–2):67–77.PubMedCrossRef
20.
go back to reference Schmidt E, et al. Serum levels of autoantibodies to BP180 correlate with disease activity in patients with bullous pemphigoid. Arch Dermatol. 2000;136(2):174–8.PubMedCrossRef Schmidt E, et al. Serum levels of autoantibodies to BP180 correlate with disease activity in patients with bullous pemphigoid. Arch Dermatol. 2000;136(2):174–8.PubMedCrossRef
21.
go back to reference Iwata Y, et al. Correlation of IgE autoantibody to BP180 with a severe form of bullous pemphigoid. Arch Dermatol. 2008;144(1):41–8.PubMedCrossRef Iwata Y, et al. Correlation of IgE autoantibody to BP180 with a severe form of bullous pemphigoid. Arch Dermatol. 2008;144(1):41–8.PubMedCrossRef
22.
go back to reference Zhang L, et al. Bullous pemphigoid: The role of type 2 inflammation in its pathogenesis and the prospect of targeted therapy. Front Immunol. 2023;14:1115083.PubMedPubMedCentralCrossRef Zhang L, et al. Bullous pemphigoid: The role of type 2 inflammation in its pathogenesis and the prospect of targeted therapy. Front Immunol. 2023;14:1115083.PubMedPubMedCentralCrossRef
23.
go back to reference Saniklidou AH, et al. IgE autoantibodies and their association with the disease activity and phenotype in bullous pemphigoid: a systematic review. Arch Dermatol Res. 2018;310(1):11–28.PubMedCrossRef Saniklidou AH, et al. IgE autoantibodies and their association with the disease activity and phenotype in bullous pemphigoid: a systematic review. Arch Dermatol Res. 2018;310(1):11–28.PubMedCrossRef
24.
go back to reference Rice JB, et al. Long-term systemic corticosteroid exposure: a systematic literature review. Clin Ther. 2017;39(11):2216–29.PubMedCrossRef Rice JB, et al. Long-term systemic corticosteroid exposure: a systematic literature review. Clin Ther. 2017;39(11):2216–29.PubMedCrossRef
25.
go back to reference Joly P, et al. A comparison of oral and topical corticosteroids in patients with bullous pemphigoid. N Engl J Med. 2002;346(5):321–7.PubMedCrossRef Joly P, et al. A comparison of oral and topical corticosteroids in patients with bullous pemphigoid. N Engl J Med. 2002;346(5):321–7.PubMedCrossRef
26.
go back to reference Feliciani C, et al. Management of bullous pemphigoid: the European Dermatology Forum consensus in collaboration with the European Academy of Dermatology and Venereology. Br J Dermatol. 2015;172(4):867–77.PubMedCrossRef Feliciani C, et al. Management of bullous pemphigoid: the European Dermatology Forum consensus in collaboration with the European Academy of Dermatology and Venereology. Br J Dermatol. 2015;172(4):867–77.PubMedCrossRef
27.
go back to reference Zeng FAP, et al. Side effects of steroid-sparing agents in patients with bullous pemphigoid and pemphigus: a systematic review. JAAD Int. 2022;9:33–43.PubMedPubMedCentralCrossRef Zeng FAP, et al. Side effects of steroid-sparing agents in patients with bullous pemphigoid and pemphigus: a systematic review. JAAD Int. 2022;9:33–43.PubMedPubMedCentralCrossRef
28.
go back to reference Bystryn JC. Comparative effectiveness of azathioprine or mycophenolate mofetil as an adjuvant for the treatment of bullous pemphigoid. Arch Dermatol. 2008;144(7):946.PubMedCrossRef Bystryn JC. Comparative effectiveness of azathioprine or mycophenolate mofetil as an adjuvant for the treatment of bullous pemphigoid. Arch Dermatol. 2008;144(7):946.PubMedCrossRef
29.
go back to reference Fivenson DP, et al. Nicotinamide and tetracycline therapy of bullous pemphigoid. Arch Dermatol. 1994;130(6):753–8.PubMedCrossRef Fivenson DP, et al. Nicotinamide and tetracycline therapy of bullous pemphigoid. Arch Dermatol. 1994;130(6):753–8.PubMedCrossRef
30.
go back to reference Wojtczak M, et al. Can methotrexate be employed as monotherapy for bullous pemphigoid? Analysis of efficiency and tolerance of methotrexate treatment in patients with bullous pemphigoid. J Clin Med. 2023;12(4):1638.PubMedPubMedCentralCrossRef Wojtczak M, et al. Can methotrexate be employed as monotherapy for bullous pemphigoid? Analysis of efficiency and tolerance of methotrexate treatment in patients with bullous pemphigoid. J Clin Med. 2023;12(4):1638.PubMedPubMedCentralCrossRef
31.
go back to reference Du-Thanh A, et al. Combined treatment with low-dose methotrexate and initial short-term superpotent topical steroids in bullous pemphigoid: an open, multicentre, retrospective study. Br J Dermatol. 2011;165(6):1337–43.PubMedCrossRef Du-Thanh A, et al. Combined treatment with low-dose methotrexate and initial short-term superpotent topical steroids in bullous pemphigoid: an open, multicentre, retrospective study. Br J Dermatol. 2011;165(6):1337–43.PubMedCrossRef
32.
go back to reference Bouscarat F, et al. Treatment of bullous pemphigoid with dapsone: retrospective study of thirty-six cases. J Am Acad Dermatol. 1996;34(4):683–4.PubMedCrossRef Bouscarat F, et al. Treatment of bullous pemphigoid with dapsone: retrospective study of thirty-six cases. J Am Acad Dermatol. 1996;34(4):683–4.PubMedCrossRef
33.
go back to reference Barthelemy H, et al. Cyclosporin in the treatment of bullous pemphigoid: preliminary study. Ann Dermatol Venereol. 1986;113(4):309–13.PubMed Barthelemy H, et al. Cyclosporin in the treatment of bullous pemphigoid: preliminary study. Ann Dermatol Venereol. 1986;113(4):309–13.PubMed
34.
go back to reference Kremer N, et al. Rituximab and omalizumab for the treatment of bullous pemphigoid: a systematic review of the literature. Am J Clin Dermatol. 2019;20(2):209–16.PubMedCrossRef Kremer N, et al. Rituximab and omalizumab for the treatment of bullous pemphigoid: a systematic review of the literature. Am J Clin Dermatol. 2019;20(2):209–16.PubMedCrossRef
35.
go back to reference Garrido PM, et al. Emerging treatments for bullous pemphigoid. J Dermatolog Treat. 2022;33(2):649–61.PubMedCrossRef Garrido PM, et al. Emerging treatments for bullous pemphigoid. J Dermatolog Treat. 2022;33(2):649–61.PubMedCrossRef
36.
go back to reference Huang H, Benoist C, Mathis D. Rituximab specifically depletes short-lived autoreactive plasma cells in a mouse model of inflammatory arthritis. Proc Natl Acad Sci U S A. 2010;107(10):4658–63.PubMedPubMedCentralCrossRefADS Huang H, Benoist C, Mathis D. Rituximab specifically depletes short-lived autoreactive plasma cells in a mouse model of inflammatory arthritis. Proc Natl Acad Sci U S A. 2010;107(10):4658–63.PubMedPubMedCentralCrossRefADS
37.
go back to reference Thomas RM, Colon A, Motaparthi K. Rituximab in autoimmune pemphigoid diseases: indications, optimized regimens, and practice gaps. Clin Dermatol. 2020;38(3):384–96.PubMedCrossRef Thomas RM, Colon A, Motaparthi K. Rituximab in autoimmune pemphigoid diseases: indications, optimized regimens, and practice gaps. Clin Dermatol. 2020;38(3):384–96.PubMedCrossRef
38.
go back to reference Amber KT, et al. Targeted therapies for autoimmune bullous diseases: current status. Drugs. 2018;78(15):1527–48.PubMedCrossRef Amber KT, et al. Targeted therapies for autoimmune bullous diseases: current status. Drugs. 2018;78(15):1527–48.PubMedCrossRef
39.
go back to reference Berkani N, et al. B-cell depletion induces a shift in self antigen specific B-cell repertoire and cytokine pattern in patients with bullous pemphigoid. Sci Rep. 2019;9(1):3525.PubMedPubMedCentralCrossRefADS Berkani N, et al. B-cell depletion induces a shift in self antigen specific B-cell repertoire and cytokine pattern in patients with bullous pemphigoid. Sci Rep. 2019;9(1):3525.PubMedPubMedCentralCrossRefADS
40.
go back to reference Polansky M, et al. Rituximab therapy in patients with bullous pemphigoid: a retrospective study of 20 patients. J Am Acad Dermatol. 2019;81(1):179–86.PubMedCrossRef Polansky M, et al. Rituximab therapy in patients with bullous pemphigoid: a retrospective study of 20 patients. J Am Acad Dermatol. 2019;81(1):179–86.PubMedCrossRef
41.
go back to reference Tovanabutra N, Payne AS. Clinical outcome and safety of rituximab therapy for pemphigoid diseases. J Am Acad Dermatol. 2020;82(5):1237–9.PubMedCrossRef Tovanabutra N, Payne AS. Clinical outcome and safety of rituximab therapy for pemphigoid diseases. J Am Acad Dermatol. 2020;82(5):1237–9.PubMedCrossRef
42.
go back to reference Hall RP 3rd, et al. Association of serum B-cell activating factor level and proportion of memory and transitional B cells with clinical response after rituximab treatment of bullous pemphigoid patients. J Invest Dermatol. 2013;133(12):2786–8.PubMedCrossRef Hall RP 3rd, et al. Association of serum B-cell activating factor level and proportion of memory and transitional B cells with clinical response after rituximab treatment of bullous pemphigoid patients. J Invest Dermatol. 2013;133(12):2786–8.PubMedCrossRef
45.
go back to reference Chiorean RM, et al. Complement-activating capacity of autoantibodies correlates with disease activity in bullous pemphigoid patients. Front Immunol. 2018;9:2687.PubMedPubMedCentralCrossRef Chiorean RM, et al. Complement-activating capacity of autoantibodies correlates with disease activity in bullous pemphigoid patients. Front Immunol. 2018;9:2687.PubMedPubMedCentralCrossRef
46.
go back to reference Wallet-Faber N, et al. Epidermolysis bullosa acquisita following bullous pemphigoid, successfully treated with the anti-CD20 monoclonal antibody rituximab. Dermatology. 2007;215(3):252–5.PubMedCrossRef Wallet-Faber N, et al. Epidermolysis bullosa acquisita following bullous pemphigoid, successfully treated with the anti-CD20 monoclonal antibody rituximab. Dermatology. 2007;215(3):252–5.PubMedCrossRef
47.
go back to reference Chen Q, et al. Three cases of refractory bullous pemphigoid in the elderly treated successfully with ultra-low-dose rituximab. J Dermatol. 2023;50(4):561–4.PubMedCrossRef Chen Q, et al. Three cases of refractory bullous pemphigoid in the elderly treated successfully with ultra-low-dose rituximab. J Dermatol. 2023;50(4):561–4.PubMedCrossRef
48.
go back to reference Suarez-Carantona C, et al. Low-dose rituximab for bullous pemphigoid. Protocol and single-center experience. Actas Dermosifiliogr. 2023;114(1):T62–8.PubMedCrossRef Suarez-Carantona C, et al. Low-dose rituximab for bullous pemphigoid. Protocol and single-center experience. Actas Dermosifiliogr. 2023;114(1):T62–8.PubMedCrossRef
49.
go back to reference Cho YT, Chu CY, Wang LF. First-line combination therapy with rituximab and corticosteroids provides a high complete remission rate in moderate-to-severe bullous pemphigoid. Br J Dermatol. 2015;173(1):302–4.PubMedCrossRef Cho YT, Chu CY, Wang LF. First-line combination therapy with rituximab and corticosteroids provides a high complete remission rate in moderate-to-severe bullous pemphigoid. Br J Dermatol. 2015;173(1):302–4.PubMedCrossRef
50.
go back to reference Annunziato F, Romagnani C, Romagnani S. The 3 major types of innate and adaptive cell-mediated effector immunity. J Allergy Clin Immunol. 2015;135(3):626–35.PubMedCrossRef Annunziato F, Romagnani C, Romagnani S. The 3 major types of innate and adaptive cell-mediated effector immunity. J Allergy Clin Immunol. 2015;135(3):626–35.PubMedCrossRef
52.
53.
go back to reference Fang H, Li Q, Wang G. The role of T cells in pemphigus vulgaris and bullous pemphigoid. Autoimmun Rev. 2020;19(11): 102661.PubMedCrossRef Fang H, Li Q, Wang G. The role of T cells in pemphigus vulgaris and bullous pemphigoid. Autoimmun Rev. 2020;19(11): 102661.PubMedCrossRef
54.
go back to reference Tavakolpour S. Dupilumab: a revolutionary emerging drug in atopic dermatitis and its possible role in pemphigus. Dermatol Ther. 2016;29(5):299.PubMedCrossRef Tavakolpour S. Dupilumab: a revolutionary emerging drug in atopic dermatitis and its possible role in pemphigus. Dermatol Ther. 2016;29(5):299.PubMedCrossRef
55.
go back to reference Takamura S, Teraki Y. Treatment of bullous pemphigoid with dupilumab: Dupilumab exerts its effect by primarily suppressing T-helper 2 cytokines. J Dermatol. 2022;49(9):845–50.PubMedCrossRef Takamura S, Teraki Y. Treatment of bullous pemphigoid with dupilumab: Dupilumab exerts its effect by primarily suppressing T-helper 2 cytokines. J Dermatol. 2022;49(9):845–50.PubMedCrossRef
56.
go back to reference Feliciani C, et al. A Th2-like cytokine response is involved in bullous pemphigoid. The role of IL-4 and IL-5 in the pathogenesis of the disease. Int J Immunopathol Pharmacol. 1999;12(2):55–61.PubMedCrossRef Feliciani C, et al. A Th2-like cytokine response is involved in bullous pemphigoid. The role of IL-4 and IL-5 in the pathogenesis of the disease. Int J Immunopathol Pharmacol. 1999;12(2):55–61.PubMedCrossRef
57.
go back to reference Giomi B, et al. Th1, Th2 and Th3 cytokines in the pathogenesis of bullous pemphigoid. J Dermatol Sci. 2002;30(2):116–28.PubMedCrossRef Giomi B, et al. Th1, Th2 and Th3 cytokines in the pathogenesis of bullous pemphigoid. J Dermatol Sci. 2002;30(2):116–28.PubMedCrossRef
58.
60.
61.
go back to reference Gounni Abdelilah S, et al. Increased expression of Th2-associated chemokines in bullous pemphigoid disease. Role of eosinophils in the production and release of these chemokines. Clin Immunol. 2006;120(2):220–31.PubMedCrossRef Gounni Abdelilah S, et al. Increased expression of Th2-associated chemokines in bullous pemphigoid disease. Role of eosinophils in the production and release of these chemokines. Clin Immunol. 2006;120(2):220–31.PubMedCrossRef
62.
go back to reference Gooderham MJ, et al. Dupilumab: A review of its use in the treatment of atopic dermatitis. J Am Acad Dermatol. 2018;78(3 Suppl 1):S28–36.PubMedCrossRef Gooderham MJ, et al. Dupilumab: A review of its use in the treatment of atopic dermatitis. J Am Acad Dermatol. 2018;78(3 Suppl 1):S28–36.PubMedCrossRef
63.
go back to reference Abdat R, et al. Dupilumab as a novel therapy for bullous pemphigoid: a multicenter case series. J Am Acad Dermatol. 2020;83(1):46–52.PubMedCrossRef Abdat R, et al. Dupilumab as a novel therapy for bullous pemphigoid: a multicenter case series. J Am Acad Dermatol. 2020;83(1):46–52.PubMedCrossRef
64.
go back to reference Yang J, et al. Dupilumab combined with low-dose systemic steroid therapy improves efficacy and safety for bullous pemphigoid. Dermatol Ther. 2022;35(8): e15648.PubMedCrossRef Yang J, et al. Dupilumab combined with low-dose systemic steroid therapy improves efficacy and safety for bullous pemphigoid. Dermatol Ther. 2022;35(8): e15648.PubMedCrossRef
66.
go back to reference Seyed Jafari SM, et al. Case Report: Combination of Omalizumab and Dupilumab for Recalcitrant Bullous Pemphigoid. Front Immunol. 2020;11: 611549.PubMedCrossRef Seyed Jafari SM, et al. Case Report: Combination of Omalizumab and Dupilumab for Recalcitrant Bullous Pemphigoid. Front Immunol. 2020;11: 611549.PubMedCrossRef
67.
go back to reference Bruni M, et al. A case of nivolumab-induced bullous pemphigoid successfully treated with dupilumab. Dermatol Online J. 2022;28(2). Bruni M, et al. A case of nivolumab-induced bullous pemphigoid successfully treated with dupilumab. Dermatol Online J. 2022;28(2).
68.
69.
go back to reference Zhao L, et al. Evaluation of dupilumab in patients with bullous pemphigoid. JAMA Dermatol. 2023;159(9):953–60.PubMedCrossRef Zhao L, et al. Evaluation of dupilumab in patients with bullous pemphigoid. JAMA Dermatol. 2023;159(9):953–60.PubMedCrossRef
70.
go back to reference US National Library of Medicine, ClinicalTrials.gov. A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Dupilumab in Adult Patients with Bullous Pemphigoid, NCT04206553. 2019. Available at: https://clinicaltrials.gov/ct2/show/NCT04206553. US National Library of Medicine, ClinicalTrials.gov. A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Dupilumab in Adult Patients with Bullous Pemphigoid, NCT04206553. 2019. Available at: https://​clinicaltrials.​gov/​ct2/​show/​NCT04206553.
71.
go back to reference Pruessmann J, et al. Immunomodulator galectin-9 is increased in blood and skin of patients with bullous pemphigoid. Acta Derm Venereol. 2021;101(3):adv00419.PubMedCrossRef Pruessmann J, et al. Immunomodulator galectin-9 is increased in blood and skin of patients with bullous pemphigoid. Acta Derm Venereol. 2021;101(3):adv00419.PubMedCrossRef
72.
go back to reference Engmann J, et al. increased activity and apoptosis of eosinophils in blister fluids, skin and peripheral blood of patients with bullous pemphigoid. Acta Derm Venereol. 2017;97(4):464–71.PubMedCrossRef Engmann J, et al. increased activity and apoptosis of eosinophils in blister fluids, skin and peripheral blood of patients with bullous pemphigoid. Acta Derm Venereol. 2017;97(4):464–71.PubMedCrossRef
73.
go back to reference Gore Karaali M, et al. Tissue eosinophil levels as a marker of disease severity in bullous pemphigoid. Australas J Dermatol. 2021;62(2):e236–41.PubMedCrossRef Gore Karaali M, et al. Tissue eosinophil levels as a marker of disease severity in bullous pemphigoid. Australas J Dermatol. 2021;62(2):e236–41.PubMedCrossRef
74.
go back to reference Kridin K. Peripheral eosinophilia in bullous pemphigoid: prevalence and influence on the clinical manifestation. Br J Dermatol. 2018;179(5):1141–7.PubMedCrossRef Kridin K. Peripheral eosinophilia in bullous pemphigoid: prevalence and influence on the clinical manifestation. Br J Dermatol. 2018;179(5):1141–7.PubMedCrossRef
76.
77.
go back to reference Frezzolini A, et al. Increased expression of eotaxin and its specific receptor CCR3 in bullous pemphigoid. Eur J Dermatol. 2002;12(1):27–31.PubMed Frezzolini A, et al. Increased expression of eotaxin and its specific receptor CCR3 in bullous pemphigoid. Eur J Dermatol. 2002;12(1):27–31.PubMed
78.
go back to reference Shrikhande M, et al. Increased coexpression of eotaxin and interleukin 5 in bullous pemphigoid. Acta Derm Venereol. 2000;80(4):277–80.PubMedCrossRef Shrikhande M, et al. Increased coexpression of eotaxin and interleukin 5 in bullous pemphigoid. Acta Derm Venereol. 2000;80(4):277–80.PubMedCrossRef
79.
go back to reference Wakugawa M, et al. Elevated levels of eotaxin and interleukin-5 in blister fluid of bullous pemphigoid: correlation with tissue eosinophilia. Br J Dermatol. 2000;143(1):112–6.PubMedCrossRef Wakugawa M, et al. Elevated levels of eotaxin and interleukin-5 in blister fluid of bullous pemphigoid: correlation with tissue eosinophilia. Br J Dermatol. 2000;143(1):112–6.PubMedCrossRef
80.
go back to reference Gunther C, et al. Up-regulation of CCL11 and CCL26 is associated with activated eosinophils in bullous pemphigoid. Clin Exp Immunol. 2011;166(2):145–53.PubMedPubMedCentralCrossRef Gunther C, et al. Up-regulation of CCL11 and CCL26 is associated with activated eosinophils in bullous pemphigoid. Clin Exp Immunol. 2011;166(2):145–53.PubMedPubMedCentralCrossRef
81.
go back to reference Amber KT, et al. Mechanisms of pathogenic effects of eosinophil cationic protein and eosinophil-derived neurotoxin on human keratinocytes. Exp Dermatol. 2018;27(12):1322–7.PubMedCrossRef Amber KT, et al. Mechanisms of pathogenic effects of eosinophil cationic protein and eosinophil-derived neurotoxin on human keratinocytes. Exp Dermatol. 2018;27(12):1322–7.PubMedCrossRef
84.
go back to reference Okada S, et al. Transmigration of eosinophils through basement membrane components in vitro: synergistic effects of platelet-activating factor and eosinophil-active cytokines. Am J Respir Cell Mol Biol. 1997;16(4):455–63.PubMedCrossRef Okada S, et al. Transmigration of eosinophils through basement membrane components in vitro: synergistic effects of platelet-activating factor and eosinophil-active cytokines. Am J Respir Cell Mol Biol. 1997;16(4):455–63.PubMedCrossRef
85.
go back to reference Rudrich U, et al. Eosinophils are a major source of interleukin-31 in bullous pemphigoid. Acta Derm Venereol. 2018;98(8):766–71.PubMedCrossRef Rudrich U, et al. Eosinophils are a major source of interleukin-31 in bullous pemphigoid. Acta Derm Venereol. 2018;98(8):766–71.PubMedCrossRef
89.
go back to reference Sallusto F, Mackay CR, Lanzavecchia A. Selective expression of the eotaxin receptor CCR3 by human T helper 2 cells. Science. 1997;277(5334):2005–7.PubMedCrossRef Sallusto F, Mackay CR, Lanzavecchia A. Selective expression of the eotaxin receptor CCR3 by human T helper 2 cells. Science. 1997;277(5334):2005–7.PubMedCrossRef
90.
go back to reference Stirling RG, et al. Interleukin-5 induces CD34(+) eosinophil progenitor mobilization and eosinophil CCR3 expression in asthma. Am J Respir Crit Care Med. 2001;164(8 Pt 1):1403–9.PubMedCrossRef Stirling RG, et al. Interleukin-5 induces CD34(+) eosinophil progenitor mobilization and eosinophil CCR3 expression in asthma. Am J Respir Crit Care Med. 2001;164(8 Pt 1):1403–9.PubMedCrossRef
91.
go back to reference D’Auria L, et al. IL-5 levels in the serum and blister fluid of patients with bullous pemphigoid: correlations with eosinophil cationic protein, RANTES, IgE and disease severity. Arch Dermatol Res. 1998;290(1–2):25–7.PubMedCrossRef D’Auria L, et al. IL-5 levels in the serum and blister fluid of patients with bullous pemphigoid: correlations with eosinophil cationic protein, RANTES, IgE and disease severity. Arch Dermatol Res. 1998;290(1–2):25–7.PubMedCrossRef
92.
go back to reference Bettiol A, et al. Mepolizumab for eosinophilic granulomatosis with polyangiitis: a European multicenter observational study. Arthritis Rheumatol. 2022;74(2):295–306.PubMedCrossRef Bettiol A, et al. Mepolizumab for eosinophilic granulomatosis with polyangiitis: a European multicenter observational study. Arthritis Rheumatol. 2022;74(2):295–306.PubMedCrossRef
93.
go back to reference Han JK, et al. Mepolizumab for chronic rhinosinusitis with nasal polyps (SYNAPSE): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet Respir Med. 2021;9(10):1141–53.PubMedCrossRef Han JK, et al. Mepolizumab for chronic rhinosinusitis with nasal polyps (SYNAPSE): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet Respir Med. 2021;9(10):1141–53.PubMedCrossRef
94.
go back to reference Ortega HG, et al. Mepolizumab treatment in patients with severe eosinophilic asthma. N Engl J Med. 2014;371(13):1198–207.PubMedCrossRef Ortega HG, et al. Mepolizumab treatment in patients with severe eosinophilic asthma. N Engl J Med. 2014;371(13):1198–207.PubMedCrossRef
95.
go back to reference Pavord ID, et al. Mepolizumab for severe eosinophilic asthma (DREAM): a multicentre, double-blind, placebo-controlled trial. Lancet. 2012;380(9842):651–9.PubMedCrossRef Pavord ID, et al. Mepolizumab for severe eosinophilic asthma (DREAM): a multicentre, double-blind, placebo-controlled trial. Lancet. 2012;380(9842):651–9.PubMedCrossRef
97.
go back to reference Simon D, et al. Mepolizumab failed to affect bullous pemphigoid: a randomized, placebo-controlled, double-blind phase 2 pilot study. Allergy. 2020;75(3):669–72.PubMedCrossRef Simon D, et al. Mepolizumab failed to affect bullous pemphigoid: a randomized, placebo-controlled, double-blind phase 2 pilot study. Allergy. 2020;75(3):669–72.PubMedCrossRef
98.
go back to reference Castro M, et al. Reslizumab for inadequately controlled asthma with elevated blood eosinophil counts: results from two multicentre, parallel, double-blind, randomised, placebo-controlled, phase 3 trials. Lancet Respir Med. 2015;3(5):355–66.PubMedCrossRef Castro M, et al. Reslizumab for inadequately controlled asthma with elevated blood eosinophil counts: results from two multicentre, parallel, double-blind, randomised, placebo-controlled, phase 3 trials. Lancet Respir Med. 2015;3(5):355–66.PubMedCrossRef
99.
101.
go back to reference Rhyou HI, Han SH, Nam YH. Successful induction treatment of bullous pemphigoid using reslizumab: a case report. Allergy Asthma Clin Immunol. 2021;17(1):117.PubMedPubMedCentralCrossRef Rhyou HI, Han SH, Nam YH. Successful induction treatment of bullous pemphigoid using reslizumab: a case report. Allergy Asthma Clin Immunol. 2021;17(1):117.PubMedPubMedCentralCrossRef
102.
go back to reference Bagnasco D, et al. Anti-interleukin 5 (IL-5) and IL-5Ra biological drugs: efficacy, safety, and future perspectives in severe eosinophilic asthma. Front Med (Lausanne). 2017;4:135.PubMedCrossRef Bagnasco D, et al. Anti-interleukin 5 (IL-5) and IL-5Ra biological drugs: efficacy, safety, and future perspectives in severe eosinophilic asthma. Front Med (Lausanne). 2017;4:135.PubMedCrossRef
103.
go back to reference FitzGerald JM, et al. Benralizumab, an anti-interleukin-5 receptor alpha monoclonal antibody, as add-on treatment for patients with severe, uncontrolled, eosinophilic asthma (CALIMA): a randomised, double-blind, placebo-controlled phase 3 trial. Lancet. 2016;388(10056):2128–41.PubMedCrossRef FitzGerald JM, et al. Benralizumab, an anti-interleukin-5 receptor alpha monoclonal antibody, as add-on treatment for patients with severe, uncontrolled, eosinophilic asthma (CALIMA): a randomised, double-blind, placebo-controlled phase 3 trial. Lancet. 2016;388(10056):2128–41.PubMedCrossRef
105.
go back to reference Dresow SK, et al. IgE autoantibodies against the intracellular domain of BP180. Br J Dermatol. 2009;160(2):429–32.PubMedCrossRef Dresow SK, et al. IgE autoantibodies against the intracellular domain of BP180. Br J Dermatol. 2009;160(2):429–32.PubMedCrossRef
106.
go back to reference Provost TT, Tomasi Jr. TB. Immunopathology of bullous pemphigoid Basement membrane deposition of IgE, alternate pathway components and fibrin. Clin Exp Immunol. 1974;18(2):193–200.PubMedPubMedCentral Provost TT, Tomasi Jr. TB. Immunopathology of bullous pemphigoid Basement membrane deposition of IgE, alternate pathway components and fibrin. Clin Exp Immunol. 1974;18(2):193–200.PubMedPubMedCentral
107.
go back to reference Messingham KA, et al. Functional characterization of an IgE-class monoclonal antibody specific for the bullous pemphigoid autoantigen, BP180. Hybridoma (Larchmt). 2012;31(2):111–7.PubMedCrossRef Messingham KA, et al. Functional characterization of an IgE-class monoclonal antibody specific for the bullous pemphigoid autoantigen, BP180. Hybridoma (Larchmt). 2012;31(2):111–7.PubMedCrossRef
108.
go back to reference Kalowska M, et al. Enzyme-linked immunoassay index for anti-NC16a IgG and IgE auto-antibodies correlates with severity and activity of bullous pemphigoid. Acta Derm Venereol. 2016;96(2):191–6.PubMedCrossRef Kalowska M, et al. Enzyme-linked immunoassay index for anti-NC16a IgG and IgE auto-antibodies correlates with severity and activity of bullous pemphigoid. Acta Derm Venereol. 2016;96(2):191–6.PubMedCrossRef
109.
go back to reference Kamata A, et al. Basement membrane zone IgE deposition is associated with bullous pemphigoid disease severity and treatment results. Br J Dermatol. 2020;182(5):1221–7.PubMedCrossRef Kamata A, et al. Basement membrane zone IgE deposition is associated with bullous pemphigoid disease severity and treatment results. Br J Dermatol. 2020;182(5):1221–7.PubMedCrossRef
110.
go back to reference van Beek N, et al. Correlation of serum levels of IgE autoantibodies against BP180 with bullous pemphigoid disease activity. JAMA Dermatol. 2017;153(1):30–8.PubMedCrossRef van Beek N, et al. Correlation of serum levels of IgE autoantibodies against BP180 with bullous pemphigoid disease activity. JAMA Dermatol. 2017;153(1):30–8.PubMedCrossRef
111.
go back to reference Fania L, et al. IgE recognition of bullous pemphigoid (BP)180 and BP230 in BP patients and elderly individuals with pruritic dermatoses. Clin Immunol. 2012;143(3):236–45.PubMedCrossRef Fania L, et al. IgE recognition of bullous pemphigoid (BP)180 and BP230 in BP patients and elderly individuals with pruritic dermatoses. Clin Immunol. 2012;143(3):236–45.PubMedCrossRef
112.
go back to reference Hashimoto T, et al. Detection of IgE autoantibodies to BP180 and BP230 and their relationship to clinical features in bullous pemphigoid. Br J Dermatol. 2017;177(1):141–51.PubMedCrossRef Hashimoto T, et al. Detection of IgE autoantibodies to BP180 and BP230 and their relationship to clinical features in bullous pemphigoid. Br J Dermatol. 2017;177(1):141–51.PubMedCrossRef
113.
go back to reference Cozzani E, et al. Anti-230 kDa circulating IgE in bullous pemphigoid: relationship with disease activity. Acta Derm Venereol. 1997;77(3):236.PubMedCrossRef Cozzani E, et al. Anti-230 kDa circulating IgE in bullous pemphigoid: relationship with disease activity. Acta Derm Venereol. 1997;77(3):236.PubMedCrossRef
114.
go back to reference Ishiura N, et al. Serum levels of IgE anti-BP180 and anti-BP230 autoantibodies in patients with bullous pemphigoid. J Dermatol Sci. 2008;49(2):153–61.PubMedCrossRef Ishiura N, et al. Serum levels of IgE anti-BP180 and anti-BP230 autoantibodies in patients with bullous pemphigoid. J Dermatol Sci. 2008;49(2):153–61.PubMedCrossRef
115.
go back to reference Shih YC, et al. BP230 IgE autoantibodies in topical-steroid-resistant bullous pemphigoid. J Dermatol. 2021;48(9):1372–80.PubMedCrossRef Shih YC, et al. BP230 IgE autoantibodies in topical-steroid-resistant bullous pemphigoid. J Dermatol. 2021;48(9):1372–80.PubMedCrossRef
117.
go back to reference Balakirski G, et al. Successful treatment of bullous pemphigoid with omalizumab as corticosteroid-sparing agent: report of two cases and review of literature. J Eur Acad Dermatol Venereol. 2016;30(10):1778–82.PubMedCrossRef Balakirski G, et al. Successful treatment of bullous pemphigoid with omalizumab as corticosteroid-sparing agent: report of two cases and review of literature. J Eur Acad Dermatol Venereol. 2016;30(10):1778–82.PubMedCrossRef
118.
go back to reference James T, et al. IgE blockade in autoimmunity: Omalizumab induced remission of bullous pemphigoid. Clin Immunol. 2019;198:54–6.PubMedCrossRef James T, et al. IgE blockade in autoimmunity: Omalizumab induced remission of bullous pemphigoid. Clin Immunol. 2019;198:54–6.PubMedCrossRef
120.
go back to reference Sarrazin M, Jouen F, Duvert-Lehembre S. Refractory bullous pemphigoid with IgE anti-BP230 and IgG anti-p200 antibodies successfully treated with omalizumab. Ann Dermatol Venereol. 2021;148(1):60–2.PubMedCrossRef Sarrazin M, Jouen F, Duvert-Lehembre S. Refractory bullous pemphigoid with IgE anti-BP230 and IgG anti-p200 antibodies successfully treated with omalizumab. Ann Dermatol Venereol. 2021;148(1):60–2.PubMedCrossRef
121.
go back to reference De D, et al. Omalizumab: an underutilized treatment option in bullous pemphigoid patients with co-morbidities. J Eur Acad Dermatol Venereol. 2021;35(7):e469–72.PubMedCrossRef De D, et al. Omalizumab: an underutilized treatment option in bullous pemphigoid patients with co-morbidities. J Eur Acad Dermatol Venereol. 2021;35(7):e469–72.PubMedCrossRef
122.
go back to reference Gonul MZ, et al. Bullous pemphigoid successfully treated with omalizumab. Indian J Dermatol Venereol Leprol. 2016;82(5):577–9.PubMedCrossRef Gonul MZ, et al. Bullous pemphigoid successfully treated with omalizumab. Indian J Dermatol Venereol Leprol. 2016;82(5):577–9.PubMedCrossRef
123.
go back to reference London VA, et al. Successful treatment of bullous pemphigoid with omalizumab. Arch Dermatol. 2012;148(11):1241–3.PubMedCrossRef London VA, et al. Successful treatment of bullous pemphigoid with omalizumab. Arch Dermatol. 2012;148(11):1241–3.PubMedCrossRef
124.
go back to reference Dufour C, et al. Successful management of severe infant bullous pemphigoid with omalizumab. Br J Dermatol. 2012;166(5):1140–2.PubMedCrossRef Dufour C, et al. Successful management of severe infant bullous pemphigoid with omalizumab. Br J Dermatol. 2012;166(5):1140–2.PubMedCrossRef
125.
go back to reference Maglie R, et al. Dramatic exacerbation of bullous pemphigoid following rituximab and successful treatment with omalizumab. Eur J Dermatol. 2019;29(2):213–5.PubMedCrossRef Maglie R, et al. Dramatic exacerbation of bullous pemphigoid following rituximab and successful treatment with omalizumab. Eur J Dermatol. 2019;29(2):213–5.PubMedCrossRef
126.
127.
go back to reference Chebani R, et al. Omalizumab in the treatment of bullous pemphigoid resistant to first-line therapy: a French national multicentre retrospective study of 100 patients. Br J Dermatol. 2023;ljad369. Chebani R, et al. Omalizumab in the treatment of bullous pemphigoid resistant to first-line therapy: a French national multicentre retrospective study of 100 patients. Br J Dermatol. 2023;ljad369.
128.
go back to reference Garrido PM, et al. Dipeptidyl-peptidase IV inhibitor-associated bullous pemphigoid efficiently treated with omalizumab. Dermatol Ther. 2020;33(6): e14160.PubMedCrossRef Garrido PM, et al. Dipeptidyl-peptidase IV inhibitor-associated bullous pemphigoid efficiently treated with omalizumab. Dermatol Ther. 2020;33(6): e14160.PubMedCrossRef
129.
go back to reference Vico-Alonso C, et al. Omalizumab as an alternative therapeutic tool in the treatment of bullous pemphigoid: a case report. Dermatol Ther. 2019;32(2): e12829.PubMedCrossRef Vico-Alonso C, et al. Omalizumab as an alternative therapeutic tool in the treatment of bullous pemphigoid: a case report. Dermatol Ther. 2019;32(2): e12829.PubMedCrossRef
131.
go back to reference Beek NV, Zillikens D, Schmidt E. Bullous Autoimmune Dermatoses-Clinical Features, Diagnostic Evaluation, and Treatment Options. Dtsch Arztebl Int. 2021;118(24):413–20.PubMedPubMedCentral Beek NV, Zillikens D, Schmidt E. Bullous Autoimmune Dermatoses-Clinical Features, Diagnostic Evaluation, and Treatment Options. Dtsch Arztebl Int. 2021;118(24):413–20.PubMedPubMedCentral
132.
go back to reference Iwata H, Kitajima Y. Bullous pemphigoid: role of complement and mechanisms for blister formation within the lamina lucida. Exp Dermatol. 2013;22(6):381–5.PubMedCrossRef Iwata H, Kitajima Y. Bullous pemphigoid: role of complement and mechanisms for blister formation within the lamina lucida. Exp Dermatol. 2013;22(6):381–5.PubMedCrossRef
133.
go back to reference Lessey E, et al. Complement and cutaneous autoimmune blistering diseases. Immunol Res. 2008;41(3):223–32.PubMedCrossRef Lessey E, et al. Complement and cutaneous autoimmune blistering diseases. Immunol Res. 2008;41(3):223–32.PubMedCrossRef
134.
go back to reference Sadik CD, et al. The critical role of C5a as an initiator of neutrophil-mediated autoimmune inflammation of the joint and skin. Semin Immunol. 2018;37:21–9.PubMedCrossRef Sadik CD, et al. The critical role of C5a as an initiator of neutrophil-mediated autoimmune inflammation of the joint and skin. Semin Immunol. 2018;37:21–9.PubMedCrossRef
135.
go back to reference Sezin T, et al. Dual inhibition of complement factor 5 and leukotriene B4 synergistically suppresses murine pemphigoid disease. JCI Insight. 2019;4(15):e128239.PubMedPubMedCentralCrossRef Sezin T, et al. Dual inhibition of complement factor 5 and leukotriene B4 synergistically suppresses murine pemphigoid disease. JCI Insight. 2019;4(15):e128239.PubMedPubMedCentralCrossRef
136.
go back to reference DiScipio RG, Schraufstatter IU. The role of the complement anaphylatoxins in the recruitment of eosinophils. Int Immunopharmacol. 2007;7(14):1909–23.PubMedCrossRef DiScipio RG, Schraufstatter IU. The role of the complement anaphylatoxins in the recruitment of eosinophils. Int Immunopharmacol. 2007;7(14):1909–23.PubMedCrossRef
137.
go back to reference Zeck-Kapp G, et al. Mechanisms of human eosinophil activation by complement protein C5a and platelet-activating factor: similar functional responses are accompanied by different morphologic alterations. Allergy. 1995;50(1):34–47.PubMedCrossRef Zeck-Kapp G, et al. Mechanisms of human eosinophil activation by complement protein C5a and platelet-activating factor: similar functional responses are accompanied by different morphologic alterations. Allergy. 1995;50(1):34–47.PubMedCrossRef
138.
139.
go back to reference Mihai S, et al. Specific inhibition of complement activation significantly ameliorates autoimmune blistering disease in mice. Front Immunol. 2018;9:535.PubMedPubMedCentralCrossRef Mihai S, et al. Specific inhibition of complement activation significantly ameliorates autoimmune blistering disease in mice. Front Immunol. 2018;9:535.PubMedPubMedCentralCrossRef
140.
go back to reference Sadik CD, et al. Evaluation of nomacopan for treatment of bullous pemphigoid: a phase 2a nonrandomized controlled trial. JAMA Dermatol. 2022;158(6):641–9.PubMedPubMedCentralCrossRef Sadik CD, et al. Evaluation of nomacopan for treatment of bullous pemphigoid: a phase 2a nonrandomized controlled trial. JAMA Dermatol. 2022;158(6):641–9.PubMedPubMedCentralCrossRef
143.
go back to reference Freire, P.C., et al., Specific Inhibition of the Classical Complement Pathway Prevents C3 Deposition along the Dermal-Epidermal Junction in Bullous Pemphigoid. J Invest Dermatol, 2019. 139(12):2417-2424 e2. Freire, P.C., et al., Specific Inhibition of the Classical Complement Pathway Prevents C3 Deposition along the Dermal-Epidermal Junction in Bullous Pemphigoid. J Invest Dermatol, 2019. 139(12):2417-2424 e2.
144.
go back to reference Dias PM, Banerjee G. The role of Th17/IL-17 on eosinophilic inflammation. J Autoimmun. 2013;40:9–20.PubMedCrossRef Dias PM, Banerjee G. The role of Th17/IL-17 on eosinophilic inflammation. J Autoimmun. 2013;40:9–20.PubMedCrossRef
145.
go back to reference Holtsche MM, et al. Adjuvant treatment with secukinumab induced long term remission in a patient with severe bullous pemphigoid. J Dtsch Dermatol Ges. 2020;18(12):1478–80.PubMed Holtsche MM, et al. Adjuvant treatment with secukinumab induced long term remission in a patient with severe bullous pemphigoid. J Dtsch Dermatol Ges. 2020;18(12):1478–80.PubMed
146.
go back to reference Kamata M, et al. Secukinumab decreased circulating anti-BP180-NC16a autoantibodies in a patient with coexisting psoriasis vulgaris and bullous pemphigoid. J Dermatol. 2019;46(6):e216–7.PubMedCrossRef Kamata M, et al. Secukinumab decreased circulating anti-BP180-NC16a autoantibodies in a patient with coexisting psoriasis vulgaris and bullous pemphigoid. J Dermatol. 2019;46(6):e216–7.PubMedCrossRef
147.
go back to reference Yun JS, et al. Successful secukinumab treatment of active bullous pemphigoid and chronic severe psoriasis: a case report. Australas J Dermatol. 2022;63(2):e155–8.PubMedCrossRef Yun JS, et al. Successful secukinumab treatment of active bullous pemphigoid and chronic severe psoriasis: a case report. Australas J Dermatol. 2022;63(2):e155–8.PubMedCrossRef
148.
go back to reference Ho PH, Tsai TF. Development of bullous pemphigoid during secukinumab treatment for psoriasis. J Dermatol. 2017;44(9):e220–1.PubMedCrossRef Ho PH, Tsai TF. Development of bullous pemphigoid during secukinumab treatment for psoriasis. J Dermatol. 2017;44(9):e220–1.PubMedCrossRef
149.
153.
go back to reference Delli FS, et al. Total IgE, eosinophils, and interleukins 16, 17A, and 23 correlations in severe bullous pemphigoid and treatment implications. Dermatol Ther. 2020;33(6): e13958.PubMedCrossRef Delli FS, et al. Total IgE, eosinophils, and interleukins 16, 17A, and 23 correlations in severe bullous pemphigoid and treatment implications. Dermatol Ther. 2020;33(6): e13958.PubMedCrossRef
154.
go back to reference Plee J, et al. Integrating longitudinal serum IL-17 and IL-23 follow-up, along with autoantibodies variation, contributes to predict bullous pemphigoid outcome. Sci Rep. 2015;5:18001.PubMedPubMedCentralCrossRefADS Plee J, et al. Integrating longitudinal serum IL-17 and IL-23 follow-up, along with autoantibodies variation, contributes to predict bullous pemphigoid outcome. Sci Rep. 2015;5:18001.PubMedPubMedCentralCrossRefADS
156.
go back to reference Cole C, Amber KT. Two patients with concomitant bullous pemphigoid and psoriasis successfully treated by IL-23 inhibition. J Eur Acad Dermatol Venereol. 2023;37(11):e1339–40.PubMedCrossRef Cole C, Amber KT. Two patients with concomitant bullous pemphigoid and psoriasis successfully treated by IL-23 inhibition. J Eur Acad Dermatol Venereol. 2023;37(11):e1339–40.PubMedCrossRef
157.
go back to reference Majima Y, et al. A successful treatment with ustekinumab in a case of antilaminin-gamma1 pemphigoid associated with psoriasis. Br J Dermatol. 2013;168(6):1367–9.PubMedCrossRef Majima Y, et al. A successful treatment with ustekinumab in a case of antilaminin-gamma1 pemphigoid associated with psoriasis. Br J Dermatol. 2013;168(6):1367–9.PubMedCrossRef
158.
go back to reference Loget J, et al. A successful treatment with ustekinumab in a case of relapsing bullous pemphigoid associated with psoriasis. J Eur Acad Dermatol Venereol. 2017;31(5):e228–30.PubMedCrossRef Loget J, et al. A successful treatment with ustekinumab in a case of relapsing bullous pemphigoid associated with psoriasis. J Eur Acad Dermatol Venereol. 2017;31(5):e228–30.PubMedCrossRef
159.
go back to reference Marin M, et al. Bullous pemphigoid induced by ustekinumab: a case report. Eur J Hosp Pharm. 2021;28(1):47–9.PubMedCrossRef Marin M, et al. Bullous pemphigoid induced by ustekinumab: a case report. Eur J Hosp Pharm. 2021;28(1):47–9.PubMedCrossRef
163.
go back to reference Junghans RP, Anderson CL. The protection receptor for IgG catabolism is the beta2-microglobulin-containing neonatal intestinal transport receptor. Proc Natl Acad Sci U S A. 1996;93(11):5512–6.PubMedPubMedCentralCrossRefADS Junghans RP, Anderson CL. The protection receptor for IgG catabolism is the beta2-microglobulin-containing neonatal intestinal transport receptor. Proc Natl Acad Sci U S A. 1996;93(11):5512–6.PubMedPubMedCentralCrossRefADS
164.
166.
go back to reference Fang H, et al. Increased expression of NLRP3 inflammasome components and interleukin-18 in patients with bullous pemphigoid. J Dermatol Sci. 2016;83(2):116–23.PubMedCrossRef Fang H, et al. Increased expression of NLRP3 inflammasome components and interleukin-18 in patients with bullous pemphigoid. J Dermatol Sci. 2016;83(2):116–23.PubMedCrossRef
169.
go back to reference Nash D, Kirchhof MG. Bullous pemphigoid treated with Janus kinase inhibitor upadacitinib. JAAD Case Rep. 2023;32:81–3.PubMedCrossRef Nash D, Kirchhof MG. Bullous pemphigoid treated with Janus kinase inhibitor upadacitinib. JAAD Case Rep. 2023;32:81–3.PubMedCrossRef
170.
go back to reference Xiao Y, Xiang H, Li W. Concurrent bullous pemphigoid and plaque psoriasis successfully treated with Janus kinase inhibitor Baricitinib. Dermatol Ther. 2022;35(10): e15754.PubMedCrossRef Xiao Y, Xiang H, Li W. Concurrent bullous pemphigoid and plaque psoriasis successfully treated with Janus kinase inhibitor Baricitinib. Dermatol Ther. 2022;35(10): e15754.PubMedCrossRef
171.
go back to reference Li H, et al. Concurrent bullous pemphigoid and psoriasis vulgaris successfully treated with Janus kinase inhibitor tofacitinib: a case report and review of the literature. Int Immunopharmacol. 2023;122: 110591.PubMedCrossRef Li H, et al. Concurrent bullous pemphigoid and psoriasis vulgaris successfully treated with Janus kinase inhibitor tofacitinib: a case report and review of the literature. Int Immunopharmacol. 2023;122: 110591.PubMedCrossRef
172.
go back to reference Maglie R, et al. The cytokine milieu of bullous pemphigoid: Current and novel therapeutic targets. Front Med (Lausanne). 2023;10:1128154.PubMedCrossRef Maglie R, et al. The cytokine milieu of bullous pemphigoid: Current and novel therapeutic targets. Front Med (Lausanne). 2023;10:1128154.PubMedCrossRef
Metadata
Title
Advancements in Bullous Pemphigoid Treatment: A Comprehensive Pipeline Update
Authors
Meropi Karakioulaki
Kilian Eyerich
Aikaterini Patsatsi
Publication date
29-12-2023
Publisher
Springer International Publishing
Published in
American Journal of Clinical Dermatology / Issue 2/2024
Print ISSN: 1175-0561
Electronic ISSN: 1179-1888
DOI
https://doi.org/10.1007/s40257-023-00832-1

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