Research progress of omalizumab in the treatment of bullous pemphigoid

被引:2
作者
Ling, Xiaoya [1 ]
Shou, Xinyang [1 ]
Lou, Yufei [1 ]
Ling, Jie [1 ]
Zhang, Mengyuan [1 ]
Yu, Tugen [2 ]
Gu, Weijia [3 ]
机构
[1] Zhejiang Chinese Med Univ, Clin Med Coll 1, Hangzhou 310053, Peoples R China
[2] Zhejiang Univ Tradit Chinese Med, Affiliated Hosp 1, Zhejiang Prov Hosp Chinese Med, Hangzhou 310006, Peoples R China
[3] Zhejiang Chinese Med Univ, Sch Publ Hlth, Hangzhou 310053, Peoples R China
关键词
bullous pemphigoid; dosing frequency; immunoglobulin E; number of doses; omalizumab; ACQUIRED HEMOPHILIA-A; SERUM IGE LEVELS; DISEASE-ACTIVITY; HUMAN SKIN; AUTOANTIBODIES; PATIENT; THERAPY; BP180; AUTOIMMUNITY; PHARMACOKINETICS;
D O I
10.1111/1346-8138.16791
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 an autoimmune blistering disease associated with anti-BP180 and anti-BP230 antibodies. The pathogenic action mechanism of immunoglobulin E (IgE) antibodies in BP has been studied since the 1970s, and IgE antibodies have gradually been confirmed as being important in BP; therefore, anti-IgE therapy may be a new option for the treatment of BP. Omalizumab, as an IgE monoclonal antibody, has been increasingly used clinically to treat BP in recent years. Here, we collected 35 papers investigating omalizumab for BP treatment in a total of 83 patients, and the vast majority of patients showed varying degrees of improvement after treatment, except for a small number of patients with poor clinical outcomes. The patients were then divided into three groups according to dosing frequency and number of doses. Statistical analysis indicated that dosing frequency had little effect on clinical efficacy. While the groups with different numbers of doses were evaluated, the results concluded that clinical efficacy was affected by the number of doses, but there was no positive correlation between the number of doses and clinical efficacy.
引用
收藏
页码:575 / 587
页数:13
相关论文
共 81 条
[11]   A case of acquired haemophilia A in a patient with bullous pemphigoid and review of the Japanese literature [J].
Chijiwa, Chika ;
Kamata, Masahiro ;
Fukuyasu, Atsuko ;
Shono, Yuki ;
Takeoka, Shintaro ;
Tateishi, Mihoko ;
Fukaya, Saki ;
Hayashi, Kotaro ;
Tanaka, Takamitsu ;
Ishikawa, Takeko ;
Ohnishi, Takamitsu ;
Saito, Koji ;
Ishii, Norito ;
Hashimoto, Takashi ;
Tada, Yayoi .
EUROPEAN JOURNAL OF DERMATOLOGY, 2018, 28 (03) :422-423
[12]   Safety and tolerability of omalizumab [J].
Corren, J. ;
Casale, T. B. ;
Lanier, B. ;
Buhl, R. ;
Holgate, S. ;
Jimenez, P. .
CLINICAL AND EXPERIMENTAL ALLERGY, 2009, 39 (06) :788-797
[13]   Biologics Beyond Boundaries: Innovative Use of Biologics in Dermatology [J].
De, Abhishek ;
Chowdhury, Barnali ;
Khemka, Monika ;
Sarda, Aarti ;
Das, Sudip .
INDIAN JOURNAL OF DERMATOLOGY, 2021, 66 (03) :314-317
[14]  
De B., 2019, BRIT J DERMATOL, V180, pe146
[15]   Omalizumab: an underutilized treatment option in bullous pemphigoid patients with co-morbidities [J].
De, D. ;
Kaushik, A. ;
Handa, S. ;
Mahajan, R. ;
Schmidt, E. .
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2021, 35 (07) :E469-E472
[16]   Clinical presentation and diagnostic delay in bullous pemphigoid: a prospective nationwide cohort [J].
della Torre, R. ;
Combescure, C. ;
Cortes, B. ;
Marazza, G. ;
Beltraminelli, H. ;
Naldi, L. ;
Borradori, L. .
BRITISH JOURNAL OF DERMATOLOGY, 2012, 167 (05) :1111-1117
[17]   Identification of a potential effector function for IgE autoantibodies in the organ-specific autoimmune disease bullous pemphigoid [J].
Dimson, OG ;
Giudice, GJ ;
Fu, CL ;
Van den Bergh, F ;
Warren, SJ ;
Janson, MM ;
Fairley, JA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 120 (05) :784-788
[18]   Successful management of severe infant bullous pemphigoid with omalizumab [J].
Dufour, C. ;
Souillet, A. L. ;
Chaneliere, C. ;
Jouen, F. ;
Bodemer, C. ;
Jullien, D. ;
Cambazard, F. ;
Joly, P. ;
Reix, P. .
BRITISH JOURNAL OF DERMATOLOGY, 2012, 166 (05) :1140-1142
[19]  
Ewy S, 2019, J DRUGS DERMATOL, V18, P947
[20]   A pathogenic role for IgE in autoimmunity: Bullous pemphigoid IgE reproduces the early phase of lesion development in human skin grafted to nu/nu mice [J].
Fairley, Janet A. ;
Burnett, Christopher T. ;
Fu, Chang-Ling ;
Larson, David L. ;
Fleming, Matthew G. ;
Giudice, George J. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2007, 127 (11) :2605-2611