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抗白细胞介素-6单克隆抗体(克拉扎奇单抗)治疗移植肾慢性抗体介导性排斥反应疗效观察

Evaluation of Clazakizumab (Anti-Interleukin-6) in Patients With Treatment-Resistant Chronic Active Antibody-Mediated Rejection of Kidney Allografts.

作者信息

Jordan Stanley C, Ammerman Noriko, Choi Jua, Huang Edmund, Najjar Reiad, Peng Alice, Sethi Supreet, Sandhu Rana, Atienza Janet, Toyoda Mieko, Ge Shili, Lim Kathlyn, Gillespie Matthew, Zhang Xiaohai, Haas Mark, Vo Ashley

机构信息

Transplant Immunotherapy Program, Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California, USA.

出版信息

Kidney Int Rep. 2022 Feb 9;7(4):720-731. doi: 10.1016/j.ekir.2022.01.1074. eCollection 2022 Apr.

Abstract

INTRODUCTION

Interleukin-6 (IL-6) is an important mediator of inflammation and activation of T cells, B cells, and plasma cells. Excessive IL-6 production is linked to human diseases characterized by unregulated antibody production, including alloimmunity, where persistence of donor-specific antibodies (DSAs), chronic active antibody-mediated rejection (cAMR), and graft loss are noted. Here, we report our experience investigating clazakizumab, a novel IL-6 inhibitor, in treating human leukocyte antigen (HLA)-sensitized patients with cAMR.

METHODS

Between February 2018 and January 2019, 10 adults with biopsy-proven cAMR were enrolled in a phase 2, single-center, open-label study. Patients received clazakizumab 25 mg subcutaneously (s.c.) monthly for 12 months, with a 6-month protocol biopsy. Primary end points included patient survival, graft survival, estimated glomerular filtration rate (eGFR), and safety. Secondary end points assessed immune markers (DSAs, IgG, T-regulatory [Treg] cells). At 12 months, stable patients entered a long-term extension (LTE).

RESULTS

LTE patients received clazakizumab for >2.5 years. Mean eGFRs showed significant declines from -24 months to study initiation (0 months) (52.8 ± 14.6 to 38.11 ± 12.23 ml/min per 1.73 m,  = 0.03). However, after initiation of clazakizumab, eGFR stabilized at (41.6 ± 14.2 and 38.1 ± 20.3 ml/min per 1.73 m, at 12 and 24 months, respectively). Banff 2017 analysis of pre- and post-treatment biopsies showed reductions in g+ptc and C4d scores. DSA reductions were seen in most patients. Adverse events (AEs) were minimal, and 2 graft losses occurred, both in patients who discontinued clazakizumab therapy at 6 months and 12 months after study initiation.

CONCLUSION

In this small cohort of patients with cAMR, clazakizumab treatment showed a trend toward stabilization of eGFR and reductions in DSA and graft inflammation. No significant safety issues were observed. A randomized, placebo-controlled clinical trial (IMAGINE) of clazakizumab in cAMR treatment is underway (NCT03744910).

摘要

引言

白细胞介素-6(IL-6)是炎症以及T细胞、B细胞和浆细胞激活的重要介质。IL-6产生过多与以抗体产生失控为特征的人类疾病有关,包括同种免疫,在同种免疫中会出现供体特异性抗体(DSA)持续存在、慢性活动性抗体介导的排斥反应(cAMR)以及移植物丢失。在此,我们报告了我们使用新型IL-6抑制剂克拉扎珠单抗治疗人类白细胞抗原(HLA)致敏的cAMR患者的经验。

方法

在2018年2月至2019年1月期间,10名经活检证实为cAMR的成年人参加了一项2期单中心开放标签研究。患者每月皮下注射(s.c.)25 mg克拉扎珠单抗,共12个月,并进行为期6个月的方案活检。主要终点包括患者生存率、移植物生存率、估计肾小球滤过率(eGFR)和安全性。次要终点评估免疫标志物(DSA、IgG、调节性T细胞[Treg])。在12个月时,病情稳定的患者进入长期扩展期(LTE)。

结果

LTE患者接受克拉扎珠单抗治疗超过2.5年。平均eGFR从-24个月至研究开始(0个月)时显著下降(每1.73平方米从52.8±14.6降至38.11±12.23 ml/min,P = 0.03)。然而,在开始使用克拉扎珠单抗后,eGFR分别在12个月和24个月时稳定在(每1.73平方米41.6±14.2和38.1±20.3 ml/min)。对治疗前和治疗后的活检进行Banff 2017分析显示,g+ptc和C4d评分降低。大多数患者的DSA减少。不良事件(AE)极少,发生了2例移植物丢失,均发生在研究开始后6个月和12个月停止克拉扎珠单抗治疗的患者中。

结论

在这个小队列的cAMR患者中,克拉扎珠单抗治疗显示出eGFR趋于稳定以及DSA和移植物炎症减少的趋势。未观察到重大安全问题。一项关于克拉扎珠单抗治疗cAMR的随机、安慰剂对照临床试验(IMAGINE)正在进行中(NCT03744910)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/968b/9039906/78a68f9b7351/fx1.jpg

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