Londhe Pradnya J, Kalyanpad Yogesh, Khopkar Uday S
Department of Dermatology, Seth Gordhandas Sunderdas Medical College and King Edward Memorial Hospital, Parel, Mumbai, Maharashtra, India.
Indian J Dermatol Venereol Leprol. 2014 Jul-Aug;80(4):300-5. doi: 10.4103/0378-6323.136832.
Rituximab, a monoclonal anti-CD20 antibody, has been used with encouraging results in pemphigus. We describe herein refractory cases of pemphigus vulgaris (n = 23) and pemphigus foliaceus (n = 1) treated with rituximab in addition to steroids and immunosuppressants.
To assess the response to treatment, the duration of clinical remission, serology of the response and adverse effects of rituximab in pemphigus patients.
We recorded observations of 24 patients with pemphigus having either refractory disease in spite of high dose of steroids and immunosuppressants, corticosteroid-dependent disease, strong contraindications to corticosteroids, or severe disease. The patients were treated with infusions of one injection per week for three consecutive weeks of 375 mg of rituximab per m ² of body-surface area. One similar infusion was repeated after 3 months of 3 rd dose. We observed the clinical outcome after 6 months of 3 rd dose of rituximab and looked for complete healing of cutaneous and mucosal lesions (complete remission).
After follow-up of 7-24 months, five patients showed only partial improvement while 19 of 24 patients had a complete remission 3 months after rituximab. Of these 19 patients, 12 patients achieved complete remission and are off all systemic therapy, and the rest are continuing with no or low dose of steroids with immunosuppressants. Two patients relapsed after initial improvement; one was given moderate dose of oral steroids and immunosuppressant and the other was given repeat single dose of rituximab to control relapse.
Rituximab is able to induce a prolonged clinical remission in pemphigus after a single course of four infusions. The high cost and limited knowledge of long term adverse effects are limitations to the use of this biologic agent.
利妥昔单抗,一种单克隆抗CD20抗体,已用于治疗天疱疮,效果令人鼓舞。我们在此描述了除使用类固醇和免疫抑制剂外,还接受利妥昔单抗治疗的23例寻常型天疱疮和1例落叶型天疱疮难治性病例。
评估利妥昔单抗对天疱疮患者的治疗反应、临床缓解持续时间、反应的血清学情况及不良反应。
我们记录了24例天疱疮患者的观察结果,这些患者要么尽管使用了高剂量的类固醇和免疫抑制剂仍患有难治性疾病,要么是依赖皮质类固醇的疾病,要么有强烈的皮质类固醇禁忌证,要么患有严重疾病。患者接受每周一次输注,连续三周,每平方米体表面积输注375mg利妥昔单抗。在第三剂输注3个月后重复一次类似的输注。我们在第三剂利妥昔单抗输注6个月后观察临床结果,并寻找皮肤和黏膜病变的完全愈合(完全缓解)。
经过7至24个月的随访,5例患者仅部分改善,而24例患者中有19例在利妥昔单抗治疗3个月后完全缓解。在这19例患者中,12例实现完全缓解且停用了所有全身治疗,其余患者继续使用无或低剂量的类固醇及免疫抑制剂。2例患者在最初改善后复发;1例给予中等剂量的口服类固醇和免疫抑制剂,另1例给予重复单剂量的利妥昔单抗以控制复发。
利妥昔单抗在单次四疗程输注后能够诱导天疱疮患者实现长期临床缓解。高成本和对长期不良反应的了解有限是使用这种生物制剂的局限性。