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Efficacy and safety of low-dose interleukin 2 in the treatment of moderate-to-severe bullous pemphigoid: A single center perspective-controlled trial.
Xue, Ruzeng; Li, Guomin; Zhou, Yao; Wang, Bocheng; Xu, Yingping; Zhao, Peizhen; Teng, Lijun; Zheng, Jinjin; Liu, Hongfang; Ji, Suyun; Elston, Dirk M; Liang, Yunsheng.
Afiliação
  • Xue R; First School of Clinical Medicine, Southern Medical University, Guangzhou, China; Department of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
  • Li G; Department of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
  • Zhou Y; Department of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
  • Wang B; Department of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
  • Xu Y; Dermatology Hospital, Southern Medical University, Guangzhou, China.
  • Zhao P; Dermatology Hospital, Southern Medical University, Guangzhou, China.
  • Teng L; Department of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
  • Zheng J; Department of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
  • Liu H; Department of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
  • Ji S; Department of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
  • Elston DM; Department of Dermatology, Medical University of South Carolina, Charleston, South Carolina. Electronic address: elstond@musc.edu.
  • Liang Y; Department of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China. Electronic address: yunshengliang@aliyun.com.
J Am Acad Dermatol ; 2024 Aug 23.
Article em En | MEDLINE | ID: mdl-39182680
ABSTRACT

BACKGROUND:

Regulatory T cells (Tregs) are reduced in the peripheral blood and skin lesions of patients with bullous pemphigoid (BP). Low-dose interleukin 2 (IL-2) therapy can stimulate Tregs specifically, suggesting potential for the treatment of BP.

OBJECTIVE:

To evaluate the response to low-dose IL-2 therapy in the treatment of moderate-to-severe BP.

METHODS:

Forty-three patients with moderate-to-severe BP were included. The therapy included systemic corticosteroids with an initial dose of 0.5 mg/kg/d for moderate and 1.0 mg/kg/d for severe disease, respectively, combined with allowed immunosuppressants for the control group, whereas in addition to the same corticosteroid therapy, IL-2 (half million IU) was administered subcutaneously every other day for the treatment group for 8 weeks. The primary outcome was the number of days required to achieve disease control. Secondary outcomes included other clinical responses.

RESULTS:

The number of days required to achieve disease control with the treatment group was (7.60 ± 3.00), which was shorter than in the control group (10.43 ± 3.06) (P = .008). The total amount of systemic corticosteroids was less, and no serious infections were detected in the treatment group.

LIMITATIONS:

Single center, open-label study with short duration and small size.

CONCLUSION:

Our trial supports the potential of low-dose IL-2 therapy for patients with moderate-to-severe BP, which showed earlier treatment responses.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Acad Dermatol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Acad Dermatol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China