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纳米颗粒凝胶包裹的辅助外用利妥昔单抗治疗寻常型天疱疮的疗效评估:一项随机、双盲、安慰剂对照的试点研究。

Assessment of Efficacy of Adjuvant Topical Rituximab Encapsulated in Nanoparticle Gel in Oral Pemphigus Vulgaris: A Randomized, Double-Blind, Placebo-Controlled, Pilot Study.

作者信息

Mohta Pratik Rajendra, Khandpur Sujay, Dinda Amit Kumar, Bhat Madhusudan, Tyagi Seema, Sharma Vinod Kumar, Kalaivani Mani

机构信息

Department of Dermatology and Venereology, All India Institute of Medical Sciences, New Delhi, India.

Department of Pathology, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Indian Dermatol Online J. 2025 Jun 20;16(4):586-590. doi: 10.4103/idoj.idoj_885_24. eCollection 2025 Jul-Aug.

Abstract

BACKGROUND

Oral pemphigus vulgaris (PV) presents with persistent, painful, nonhealing oral erosions, with a slower treatment response compared to cutaneous lesions.

PATIENTS AND METHODS

To assess the efficacy of adjuvant topical rituximab encapsulated in nanoparticle gel in oral PV. Of 31 oral PV patients recruited, 16 were randomized to rituximab incorporated in calcium alginate nanoparticles (study group) and 15 to calcium alginate nanoparticle gel only (placebo group), applied twice daily on oral erosions for 12 weeks. Both groups, in addition, received oral prednisolone (tapering doses) and azathioprine.

RESULTS

In the topical rituximab group, 75% of patients and in the placebo group, 86.7% of patients achieved remission ( = 0.65) over 12 weeks of therapy. The median time to remission in the topical rituximab group was 4 weeks, and in the placebo group, it was 8 weeks ( = 0.53). Median oral pemphigus scores showed an earlier reduction in the rituximab group ( = 0.52). The median circulating CD20 count was reduced in the topical rituximab group from 100 to 74/mm at week 8. In the placebo group, the value increased from 89 to 118/mm (intergroup = 0.29). A significantly greater number of cases in the topical rituximab group had a negative mucosal CD20 count ( = 0.001). There was a comparable fall in desmoglein 3 titers in both groups ( = 0.58). The mean cumulative prednisolone dose was 3567 mg in the topical rituximab group and 3869 mg in the placebo group ( = 0.125). No side effects of rituximab were observed.

LIMITATIONS

A small sample size, and need of pharmacokinetic studies in animal models to assess absorption of rituximab in nanogel formulation.

CONCLUSION

With topical rituximab incorporated in nanogel, there was a trend toward earlier remission, lower total cumulative oral prednisolone dose, earlier improvement in oral pemphigus score, and greater reduction in CD20 count.

摘要

背景

寻常型天疱疮口腔表现为持续性、疼痛性、不愈合的口腔糜烂,与皮肤损害相比,治疗反应较慢。

患者与方法

评估纳米颗粒凝胶包裹的辅助性局部用利妥昔单抗治疗口腔寻常型天疱疮的疗效。在招募的31例口腔寻常型天疱疮患者中,16例随机分配至藻酸钙纳米颗粒包裹利妥昔单抗组(研究组),15例分配至仅使用藻酸钙纳米颗粒凝胶组(安慰剂组),每天两次涂抹于口腔糜烂处,持续12周。此外,两组均接受口服泼尼松龙(逐渐减量)和硫唑嘌呤治疗。

结果

在局部用利妥昔单抗组,75%的患者在12周治疗后病情缓解,安慰剂组为86.7%(P = 0.65)。局部用利妥昔单抗组病情缓解的中位时间为4周,安慰剂组为8周(P = 0.53)。中位口腔天疱疮评分显示利妥昔单抗组下降更早(P = 0.52)。局部用利妥昔单抗组第8周时循环CD20计数中位数从100降至74/mm³。在安慰剂组,该值从89升至118/mm³(组间P = 0.29)。局部用利妥昔单抗组黏膜CD20计数阴性的病例数显著更多(P = 0.001)。两组中桥粒芯糖蛋白3滴度下降程度相当(P = 0.58)。局部用利妥昔单抗组泼尼松龙平均累积剂量为3567mg,安慰剂组为3869mg(P = 0.125)。未观察到利妥昔单抗的副作用。

局限性

样本量小,且需要在动物模型中进行药代动力学研究以评估纳米凝胶制剂中利妥昔单抗的吸收情况。

结论

纳米凝胶包裹局部用利妥昔单抗有病情缓解更早、口服泼尼松龙总累积剂量更低、口腔天疱疮评分改善更早以及CD20计数下降更明显的趋势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/375e/12270421/cdb4b09da3c5/IDOJ-16-586-g001.jpg

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