Background: Recently, several case-control studies demonstrated an association between gliptins and bullous pemphigoid (BP) occurrence. However, data on the clinical and immunologic features of gliptin-associated bullous pemphigoid (GABP) are controversial. Objective: This study aimed to clinically and immunologically characterize a large cohort of GABP patients to get an insight into the pathophysiology of this emerging drug-induced variant of BP. Methods: Seventy-four GABP patients were prospectively enrolled and characterized from 9 different Italian dermatology units between 2013 and 2020. Results: Our findings demonstrated the following in the GABP patients: (1) a noninflammatory phenotype, which is characterized by low amounts of circulating and skin-infiltrating eosinophils, is frequently found; (2) immunoglobulin (Ig)G, IgE, and IgA humoral responses to BP180 and BP230 antigens are reduced in frequency and titers compared with those in patients with idiopathic BP; (3) IgG reactivity targets multiple BP180 epitopes other than noncollagenous region 16A. Limitations: A limitation of the study is that the control group did not comprise only type 2 diabetes mellitus patients with BP. Conclusion: GABP patients show peculiar features of anti-BP180 and -BP230 humoral responses, laying the foundation for diagnostic improvements and getting novel insights into understanding the mechanism of BP onset.

Gliptin-associated bullous pemphigoid shows peculiar features of anti-BP180 and -BP230 humoral response: Results of a multicenter study / A. Salemme, L. Fania, A. Scarabello, M. Caproni, A.V. Marzano, E. Cozzani, C. Feliciani, C. De Simone, M. Papini, R.R. Satta, A. Parodi, F. Mariotti, S. Lechiancole, G. Genovese, F. Passarelli, F. Festa, B. Bellei, A. Provini, D. Sordi, S. Pallotta, D. Abeni, C. Mazzanti, B. Didona, G. Di Zenzo. - In: JAAD INTERNATIONAL. - ISSN 2666-3287. - 87:1(2022 Jul), pp. 56-63. [10.1016/j.jaad.2022.02.036]

Gliptin-associated bullous pemphigoid shows peculiar features of anti-BP180 and -BP230 humoral response: Results of a multicenter study

A.V. Marzano;G. Genovese;
2022

Abstract

Background: Recently, several case-control studies demonstrated an association between gliptins and bullous pemphigoid (BP) occurrence. However, data on the clinical and immunologic features of gliptin-associated bullous pemphigoid (GABP) are controversial. Objective: This study aimed to clinically and immunologically characterize a large cohort of GABP patients to get an insight into the pathophysiology of this emerging drug-induced variant of BP. Methods: Seventy-four GABP patients were prospectively enrolled and characterized from 9 different Italian dermatology units between 2013 and 2020. Results: Our findings demonstrated the following in the GABP patients: (1) a noninflammatory phenotype, which is characterized by low amounts of circulating and skin-infiltrating eosinophils, is frequently found; (2) immunoglobulin (Ig)G, IgE, and IgA humoral responses to BP180 and BP230 antigens are reduced in frequency and titers compared with those in patients with idiopathic BP; (3) IgG reactivity targets multiple BP180 epitopes other than noncollagenous region 16A. Limitations: A limitation of the study is that the control group did not comprise only type 2 diabetes mellitus patients with BP. Conclusion: GABP patients show peculiar features of anti-BP180 and -BP230 humoral responses, laying the foundation for diagnostic improvements and getting novel insights into understanding the mechanism of BP onset.
English
BP180; autoantibody; bullous pemphigoid; epitope; gliptin; humoral response;
Settore MED/35 - Malattie Cutanee e Veneree
Articolo
Esperti anonimi
Pubblicazione scientifica
Goal 3: Good health and well-being
lug-2022
1-mar-2022
Elsevier : American Academy of Dermatology
87
1
56
63
8
Pubblicato
Periodico con rilevanza internazionale
pubmed
Aderisco
info:eu-repo/semantics/article
Gliptin-associated bullous pemphigoid shows peculiar features of anti-BP180 and -BP230 humoral response: Results of a multicenter study / A. Salemme, L. Fania, A. Scarabello, M. Caproni, A.V. Marzano, E. Cozzani, C. Feliciani, C. De Simone, M. Papini, R.R. Satta, A. Parodi, F. Mariotti, S. Lechiancole, G. Genovese, F. Passarelli, F. Festa, B. Bellei, A. Provini, D. Sordi, S. Pallotta, D. Abeni, C. Mazzanti, B. Didona, G. Di Zenzo. - In: JAAD INTERNATIONAL. - ISSN 2666-3287. - 87:1(2022 Jul), pp. 56-63. [10.1016/j.jaad.2022.02.036]
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A. Salemme, L. Fania, A. Scarabello, M. Caproni, A.V. Marzano, E. Cozzani, C. Feliciani, C. De Simone, M. Papini, R.R. Satta, A. Parodi, F. Mariotti, ...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/923874
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