Advancements in Bullous Pemphigoid Treatment: A Comprehensive Pipeline Update

被引:19
作者
Karakioulaki, Meropi [1 ]
Eyerich, Kilian [1 ]
Patsatsi, Aikaterini [2 ]
机构
[1] Univ Hosp Freiburg, Med Ctr, Dept Dermatol & Venerol, Freiburg, Germany
[2] Aristotle Univ Thessaloniki, Papageorgiou Hosp, Sch Med, Dept Dermatol 2, Thessaloniki, Greece
关键词
PLATELET-ACTIVATING-FACTOR; IGE AUTOANTIBODIES; INCREASED EXPRESSION; EOSINOPHILIC ASTHMA; MONOCLONAL-ANTIBODY; SERUM-LEVELS; DISEASE-ACTIVITY; BLISTER FLUID; RECEPTOR CCR3; DOUBLE-BLIND;
D O I
10.1007/s40257-023-00832-1
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
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 alpha 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.
引用
收藏
页码:195 / 212
页数:18
相关论文
共 172 条
[41]   IgE recognition of bullous pemphigoid (BP)180 and BP230 in BP patients and elderly individuals with pruritic dermatoses [J].
Fania, Luca ;
Caldarola, Giacomo ;
Mueller, Ralf ;
Brandt, Oliver ;
Pellicano, Riccardo ;
Feliciani, Claudio ;
Hertl, Michael .
CLINICAL IMMUNOLOGY, 2012, 143 (03) :236-245
[42]   Management of bullous pemphigoid: the European Dermatology Forum consensus in collaboration with the European Academy of Dermatology and Venereology [J].
Feliciani, C. ;
Joly, P. ;
Jonkman, M. F. ;
Zambruno, G. ;
Zillikens, D. ;
Ioannides, D. ;
Kowalewski, C. ;
Jedlickova, H. ;
Karpati, S. ;
Marinovic, B. ;
Mimouni, D. ;
Uzun, S. ;
Yayli, S. ;
Hertl, M. ;
Borradori, L. .
BRITISH JOURNAL OF DERMATOLOGY, 2015, 172 (04) :867-877
[43]  
Feliciani C, 1999, INT J IMMUNOPATH PH, V12, P55
[44]  
FitzGerald JM, 2016, LANCET, V388, P2128, DOI [10.1016/S0140-6736(16)31322-8, 10.1016/s0140-6736(16)31322-8]
[45]   NICOTINAMIDE AND TETRACYCLINE THERAPY OF BULLOUS PEMPHIGOID [J].
FIVENSON, DP ;
BRENEMAN, DL ;
ROSAN, GB ;
HERSH, CS ;
CARDONE, S ;
MUTASIM, D .
ARCHIVES OF DERMATOLOGY, 1994, 130 (06) :753-758
[46]   Specific Inhibition of the Classical Complement Pathway Prevents C3 Deposition along the Dermal-Epidermal Junction in Bullous Pemphigoid [J].
Freire, Patricia Colchete ;
Munoz, Cristina Herraez ;
Derhaschnig, Ulla ;
Schoergenhofer, Christian ;
Firbas, Christa ;
Parry, Graham C. ;
Panicker, Sandip ;
Gilbert, James C. ;
Stingl, Georg ;
Jilma, Bernd ;
Heil, Peter Maximilian .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2019, 139 (12) :2417-+
[47]  
Frezzolini A, 2002, EUR J DERMATOL, V12, P27
[48]   The IL-23-IL-17 immune axis: from mechanisms to therapeutic testing [J].
Gaffen, Sarah L. ;
Jain, Renu ;
Garg, Abhishek V. ;
Cua, Daniel J. .
NATURE REVIEWS IMMUNOLOGY, 2014, 14 (09) :585-600
[49]   Emerging treatments for bullous pemphigoid [J].
Garrido, Pedro Miguel ;
QueiroS, Catarina Soares ;
Travassos, Ana Rita ;
Borges-Costa, Joao ;
Filipe, Paulo .
JOURNAL OF DERMATOLOGICAL TREATMENT, 2022, 33 (02) :649-661
[50]   Dipeptidyl-peptidase IV inhibitor-associated bullous pemphigoid efficiently treated with omalizumab [J].
Garrido, Pedro Miguel ;
Alexandre, Maria Ines ;
Travassos, Ana Rita ;
Filipe, Paulo .
DERMATOLOGIC THERAPY, 2020, 33 (06)