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开发一种新型降钙素基因相关肽抗体用于治疗骨关节炎相关疼痛。

Development of a novel antibody to calcitonin gene-related peptide for the treatment of osteoarthritis-related pain.

机构信息

Eli Lilly & Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.

Eli Lilly & Company, Lilly Biotechnology Center, San Diego, CA 92121, USA.

出版信息

Osteoarthritis Cartilage. 2014 Apr;22(4):578-85. doi: 10.1016/j.joca.2014.01.009. Epub 2014 Feb 6.

Abstract

OBJECTIVE

Investigate a role for calcitonin gene-related peptide (CGRP) in osteoarthritis (OA)-related pain.

DESIGN

Neutralizing antibodies to CGRP were generated de novo. One of these antibodies, LY2951742, was characterized in vitro and tested in pre-clinical in vivo models of OA pain.

RESULTS

LY2951742 exhibited high affinity to both human and rat CGRP (KD of 31 and 246 pM, respectively). The antibody neutralized CGRP-mediated induction of cAMP in SK-N-MC cells in vitro and capsaicin-induced dermal blood flow in the rat. Neutralization of CGRP significantly reduced pain behavior as measured by weight bearing differential in the rat monoiodoacetate model of OA pain in a dose-dependent manner. Moreover, pain reduction with neutralization of CGRP occurred independently of prostaglandins, since LY2951742 and NSAIDs worked additively in the NSAID-responsive version of the model and CGRP neutralization remained effective in the NSAID non-responsive version of the model. Neutralization of CGRP also provided dose-dependent and prolonged (>60 days) pain reduction in the rat meniscal tear model of OA after only a single injection of LY2951742.

CONCLUSIONS

LY2951742 is a high affinity, neutralizing antibody to CGRP. Neutralization of CGRP is efficacious in several OA pain models and works independently of NSAID mechanisms of action. LY2951742 holds promise for the treatment of pain in OA patients.

摘要

目的

研究降钙素基因相关肽(CGRP)在骨关节炎(OA)相关疼痛中的作用。

设计

从头生成针对 CGRP 的中和抗体。其中一种抗体,LY2951742,在体外进行了表征,并在 OA 疼痛的临床前体内模型中进行了测试。

结果

LY2951742对人和大鼠 CGRP 均表现出高亲和力(KD 分别为 31 和 246 pM)。该抗体在体外中和 CGRP 介导的 SK-N-MC 细胞中环磷酸腺苷的诱导作用,并中和辣椒素诱导的大鼠皮肤血流。中和 CGRP 显著降低了大鼠单碘乙酸盐 OA 疼痛模型中体重差异测量的疼痛行为,呈剂量依赖性。此外,由于 LY2951742 和 NSAIDs 在 NSAID 反应模型中具有相加作用,而 CGRP 中和在 NSAID 非反应模型中仍然有效,因此 CGRP 的中和与前列腺素无关。LY2951742 单次注射后,还可在大鼠半月板撕裂 OA 模型中提供剂量依赖性和持久(>60 天)的疼痛缓解。

结论

LY2951742 是一种对 CGRP 具有高亲和力的中和抗体。中和 CGRP 在几种 OA 疼痛模型中有效,并且独立于 NSAID 的作用机制。LY2951742 有望用于治疗 OA 患者的疼痛。

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