Dörner Thomas, Kaufmann Joerg, Wegener William A, Teoh Nick, Goldenberg David M, Burmester Gerd R
Department of Medicine/Rheumatology and Clinical Immunology, Charite Hospital, Berlin, Germany.
Arthritis Res Ther. 2006;8(3):R74. doi: 10.1186/ar1942. Epub 2006 Apr 21.
B cells play an important role in the pathogenesis of systemic lupus erythematosus (SLE), so the safety and activity of anti-B cell immunotherapy with the humanized anti-CD22 antibody epratuzumab was evaluated in SLE patients. An open-label, single-center study of 14 patients with moderately active SLE (total British Isles Lupus Assessment Group (BILAG) score 6 to 12) was conducted. Patients received 360 mg/m2 epratuzumab intravenously every 2 weeks for 4 doses with analgesic/antihistamine premedication (but no steroids) prior to each dose. Evaluations at 6, 10, 18 and 32 weeks (6 months post-treatment) follow-up included safety, SLE activity (BILAG score), blood levels of epratuzumab, B and T cells, immunoglobulins, and human anti-epratuzumab antibody (HAHA) titers. Total BILAG scores decreased by > or = 50% in all 14 patients at some point during the study (including 77% with a > or = 50% decrease at 6 weeks), with 92% having decreases of various amounts continuing to at least 18 weeks (where 38% showed a >/= 50% decrease). Almost all patients (93%) experienced improvements in at least one BILAG B- or C-level disease activity at 6, 10 and 18 weeks. Additionally, 3 patients with multiple BILAG B involvement at baseline had completely resolved all B-level disease activities by 18 weeks. Epratuzumab was well tolerated, with a median infusion time of 32 minutes. Drug serum levels were measurable for at least 4 weeks post-treatment and detectable in most samples at 18 weeks. B cell levels decreased by an average of 35% at 18 weeks and remained depressed at 6 months post-treatment. Changes in routine safety laboratory tests were infrequent and without any consistent pattern, and there was no evidence of immunogenicity or significant changes in T cells, immunoglobulins, or autoantibody levels. In patients with mild to moderate active lupus, 360 mg/m2 epratuzumab was well tolerated, with evidence of clinical improvement after the first infusion and durable clinical benefit across most body systems. As such, multicenter controlled studies are being conducted in broader patient populations.
B细胞在系统性红斑狼疮(SLE)的发病机制中起重要作用,因此在SLE患者中评估了人源化抗CD22抗体依帕珠单抗抗B细胞免疫疗法的安全性和活性。对14例中度活动性SLE患者(不列颠群岛狼疮评估组(BILAG)总分6至12分)进行了一项开放标签、单中心研究。患者每2周静脉注射360 mg/m²依帕珠单抗,共4剂,每次给药前给予镇痛/抗组胺预处理(但不使用类固醇)。在6、10、18和32周(治疗后6个月)随访时的评估包括安全性、SLE活动度(BILAG评分)、依帕珠单抗的血药浓度、B细胞和T细胞、免疫球蛋白以及人抗依帕珠单抗抗体(HAHA)滴度。在研究期间的某个时间点,所有14例患者的BILAG总分均下降了≥50%(包括77%的患者在6周时下降了≥50%),92%的患者下降幅度各异,至少持续到18周(其中38%的患者下降幅度≥50%)。几乎所有患者(93%)在6、10和18周时至少有一项BILAG B级或C级疾病活动度得到改善。此外,3例基线时多项BILAG B级受累的患者在18周时所有B级疾病活动度完全缓解。依帕珠单抗耐受性良好,中位输注时间为32分钟。治疗后至少4周可检测到药物血清浓度,并在18周时在大多数样本中可检测到。B细胞水平在18周时平均下降35%,在治疗后6个月仍处于较低水平。常规安全性实验室检查变化不常见,且无任何一致模式,也没有免疫原性证据或T细胞、免疫球蛋白或自身抗体水平的显著变化。在轻至中度活动性狼疮患者中,360 mg/m²依帕珠单抗耐受性良好,首次输注后有临床改善的证据,且对大多数身体系统有持久的临床益处。因此,正在更广泛的患者群体中进行多中心对照研究。
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