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In Vitro and In Vivo Evaluation of a Humanized Anti-APRIL Antibody.

机译:人源化抗APRIL抗体的体外和体内评估。

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A proliferation-inducing ligand (APRIL) is overexpressed in many cancers such as colorectal, gastric and liver. Silence APRIL gene or neutralize its expression may serve as therapeutic strategies to manage those cancers. Current phase I clinical trial shows that heavily pretreated patients were well tolerated high dose intravenous infusion. Herein, we report a humanized antibody (Ab) that neutralizes APRIL protein and inhibits cancer cell proliferation both in vitro and in vivo. The Ab was generated through conjugating foreign immunodominant T-helper cell (Th) epitopes to the N- or C-terminal of four soluble APRIL mutants. In vitro anti-proliferation effects were evaluated in both Raji and Jurkat cell lines. In vivo inhibition of tumor growth was determined in a tumor xenograft animal model with green fluorescent protein (GFP) positive Raji cell line. In vitro data demonstrated that this Ab significantly inhibited both Raji and Jurkat cell proliferation in a dose-dependent manner. The molecular imaging data demonstrated in vivo tumor growth delay when animals were treated with Ab. In conclusion, we have developed a humanized anti-APRIL Ab, which is effective in inhibiting tumor cell proliferations both in vitro and vivo. The humanized Ab has potential to reduce the immunoresponse in the clinical situation. This Ab also can be used in other APRIL mediated diseases such as Sjogren syndrome, multiple sclerosis and systemic lupus erythematosus.
机译:诱导增殖的配体(APRIL)在许多癌症(例如大肠癌,胃癌和肝癌)中过表达。使APRIL基因沉默或中和其表达可能作为治疗那些癌症的治疗策略。当前的I期临床试验表明,经过大量预处理的患者对高剂量静脉输液的耐受性良好。本文中,我们报道了一种人源化抗体(Ab),该抗体可中和APRIL蛋白并在体外和体内抑制癌细胞的增殖。通过将外来免疫优势T辅助细胞(Th)表位缀合到四个可溶性APRIL突变体的N或C末端来产生Ab。在Raji和Jurkat细胞系中均评估了体外抗增殖作用。在具有绿色荧光蛋白(GFP)阳性Raji细胞系的肿瘤异种移植动物模型中确定体内抑制肿瘤生长。体外数据表明,该抗体以剂量依赖性方式显着抑制Raji和Jurkat细胞增殖。分子成像数据显示,当用Ab治疗动物时,体内肿瘤生长会延迟。总之,我们已经开发出一种人源化的抗APRIL Ab,在体外和体内均可有效抑制肿瘤细胞的增殖。人源化抗体具有降低临床情况下免疫反应的潜力。该Ab也可用于其他APRIL介导的疾病,例如Sjogren综合征,多发性硬化症和系统性红斑狼疮。

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