Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 Feb 16:14:1115083.
doi: 10.3389/fimmu.2023.1115083. eCollection 2023.

Bullous pemphigoid: The role of type 2 inflammation in its pathogenesis and the prospect of targeted therapy

Affiliations
Review

Bullous pemphigoid: The role of type 2 inflammation in its pathogenesis and the prospect of targeted therapy

Luyao Zhang et al. Front Immunol. .

Abstract

Bullous pemphigoid (BP) is an autoimmune disease that mainly occurs in the elderly, severely affecting their health and life quality. Traditional therapy for BP is mainly based on the systemic use of corticosteroids, but long-term use of corticosteroids results in a series of side effects. Type 2 inflammation is an immune response largely mediated by group 2 innate lymphoid cells, type 2 T helper cells, eosinophils, and inflammatory cytokines, such as interleukin (IL)-4, IL-5 and IL-13. Among patients with BP, the levels of immunoglobulin E and eosinophils are significantly increased in the peripheral blood and skin lesions, suggesting that the pathogenesis is tightly related to type 2 inflammation. To date, various targeted drugs have been developed to treat type 2 inflammatory diseases. In this review, we summarize the general process of type 2 inflammation, its role in the pathogenesis of BP and potential therapeutic targets and medications related to type 2 inflammation. The content of this review may contribute to the development of more effective drugs with fewer side effects for the treatment of BP.

Keywords: bullous pemphigoid; eosinophils; immunoglobulin E; targeted therapy; type 2 inflammation.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
General process of type 2 inflammation (by Figdraw).

References

    1. Persson MSM, Begum N, Grainge MJ, Harman KE, Grindlay D, Gran S. The global incidence of bullous pemphigoid: A systematic review and meta-analysis. Br J Dermatol (2022) 186(3):414–25. doi: 10.1111/bjd.20743 - DOI - PubMed
    1. Bağcı IS, Horváth ON, Ruzicka T, Sárdy M. Bullous pemphigoid. Autoimmun Rev (2017) 16(5):445–55. doi: 10.1016/j.autrev.2017.03.010 - DOI - PubMed
    1. Kridin K, Schwartz N, Cohen AD, Zelber-Sagi S. Mortality in bullous pemphigoid: A systematic review and meta-analysis of standardized mortality ratios. J Dermatol (2018) 45(9):1094–100. doi: 10.1111/1346-8138.14503 - DOI - PubMed
    1. Maronese CA, Caproni M, Moltrasio C, Genovese G, Vezzoli P, Sena P, et al. Bullous pemphigoid associated with covid-19 vaccines: An Italian multicentre study. Front Med (2022) 9:841506. doi: 10.3389/fmed.2022.841506 - DOI - PMC - PubMed
    1. Salemme A, Fania L, Scarabello A, Caproni M, Marzano AV, Cozzani E, 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. doi: 10.1016/j.jaad.2022.02.036 - DOI - PubMed

Publication types