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本文引用的文献

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The sweet spot: how GAGs help chemokines guide migrating cells.最佳点:糖胺聚糖如何帮助趋化因子引导迁移细胞。
J Leukoc Biol. 2016 Jun;99(6):935-53. doi: 10.1189/jlb.3MR0915-440R. Epub 2015 Dec 23.
2
The Concise Guide to PHARMACOLOGY 2015/16: G protein-coupled receptors.《2015/16药理学简明指南:G蛋白偶联受体》
Br J Pharmacol. 2015 Dec;172(24):5744-869. doi: 10.1111/bph.13348.
3
The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands.《2016年IUPHAR/BPS药理学指南:迈向1300个蛋白质靶点与6000种配体之间的精准定量相互作用》
Nucleic Acids Res. 2016 Jan 4;44(D1):D1054-68. doi: 10.1093/nar/gkv1037. Epub 2015 Oct 12.
4
Cross-reactive and pre-existing antibodies to therapeutic antibodies--Effects on treatment and immunogenicity.治疗性抗体的交叉反应性和预先存在的抗体——对治疗和免疫原性的影响。
MAbs. 2015;7(4):662-71. doi: 10.1080/19420862.2015.1048411.
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GSK2374697, a novel albumin-binding domain antibody (AlbudAb), extends systemic exposure of exendin-4: first study in humans--PK/PD and safety.GSK2374697,一种新型的白蛋白结合域抗体(AlbudAb),可延长外泌肽-4的系统暴露:在人体中的首次研究——药代动力学/药效学和安全性。
Clin Pharmacol Ther. 2014 Dec;96(6):704-12. doi: 10.1038/clpt.2014.187. Epub 2014 Sep 19.
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Assessment and reporting of the clinical immunogenicity of therapeutic proteins and peptides-harmonized terminology and tactical recommendations.治疗性蛋白和肽的临床免疫原性评估和报告——术语协调和策略建议。
AAPS J. 2014 Jul;16(4):658-73. doi: 10.1208/s12248-014-9599-2. Epub 2014 Apr 24.
7
A randomized, controlled trial to evaluate the effect of an anti-interleukin-9 monoclonal antibody in adults with uncontrolled asthma.一项评估抗白细胞介素-9 单克隆抗体在未控制的哮喘成人中的疗效的随机、对照试验。
Respir Res. 2013 Sep 19;14(1):93. doi: 10.1186/1465-9921-14-93.
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Investigation of the cutaneous response to recall antigen in humans in vivo.体内人体对回忆抗原的皮肤反应研究。
Clin Exp Immunol. 2013 Aug;173(2):163-72. doi: 10.1111/cei.12107.
9
A first-in-human, first-in-class, phase I study of carlumab (CNTO 888), a human monoclonal antibody against CC-chemokine ligand 2 in patients with solid tumors.一项在实体瘤患者中进行的人源化单克隆抗体 carlumab(CNTO 888)的首次人体、首次同类、I 期研究,该抗体针对 CC-趋化因子配体 2。
Cancer Chemother Pharmacol. 2013 Apr;71(4):1041-50. doi: 10.1007/s00280-013-2099-8. Epub 2013 Feb 6.
10
CCR6 is required for epidermal trafficking of γδ-T cells in an IL-23-induced model of psoriasiform dermatitis.CCR6 对于 γδ-T 细胞在白细胞介素 23 诱导的银屑病样皮炎模型中的表皮转运是必需的。
J Invest Dermatol. 2013 Jan;133(1):164-71. doi: 10.1038/jid.2012.260. Epub 2012 Aug 16.

在健康受试者中,通过单克隆抗体中和 CCL20 可选择性抑制实验性抽吸性水疱中 CCR6 细胞的募集。

CCL20 neutralization by a monoclonal antibody in healthy subjects selectively inhibits recruitment of CCR6 cells in an experimental suction blister.

机构信息

GlaxoSmithKline, Hertfordshire, UK.

GSK Clinical Unit, Cambridge, UK.

出版信息

Br J Clin Pharmacol. 2017 Sep;83(9):1976-1990. doi: 10.1111/bcp.13286. Epub 2017 Apr 22.

DOI:10.1111/bcp.13286
PMID:28295451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5555862/
Abstract

AIMS

GSK3050002, a humanized IgG1κ antibody with high binding affinity to human CCL20, was administered in a first-in-human study to evaluate safety, pharmacokinetics (PK) and pharmacodynamics (PD). An experimental skin suction blister model was employed to assess target engagement and the ability of the compound to inhibit recruitment of inflammatory CCR6 expressing cells.

METHODS

This study was a randomized, double-blind (sponsor open), placebo-controlled, single-centre, single ascending intravenous dose escalation trial in 48 healthy male volunteers.

RESULTS

GSK3050002 (0.1-20 mg kg ) was well tolerated and no safety concerns were identified. The PK was linear over the dose range, with a half-life of approximately 2 weeks. Complex of GSK3050002/CCL20 increased in serum and blister fluid with increasing doses of GSK3050002. There were dose-dependent decreases in CCR6 cell recruitment to skin blisters with maximal effects at doses of 5 mg kg and higher, doses at which GSK3050002/CCL20 complex in serum and blister fluid also appeared to reach maximum levels.

CONCLUSIONS

These results indicate a relationship between PK, target engagement and PD, suggesting a selective inhibition of recruitment of CCR6 cells by GSK3050002 and support further development of GSK3050002 in autoimmune and inflammatory diseases.

摘要

目的

GSK3050002 是一种人源化 IgG1κ 抗体,对人 CCL20 具有高亲和力,在首次人体研究中进行了给药,以评估安全性、药代动力学(PK)和药效动力学(PD)。采用实验性皮肤抽吸水疱模型评估了靶标结合和化合物抑制炎症性 CCR6 表达细胞募集的能力。

方法

这是一项在 48 名健康男性志愿者中进行的随机、双盲(研究者开放)、安慰剂对照、单中心、单递增静脉内剂量递增试验。

结果

GSK3050002(0.1-20mg/kg)耐受性良好,未发现安全性问题。PK 在剂量范围内呈线性,半衰期约为 2 周。随着 GSK3050002 剂量的增加,GSK3050002/CCL20 复合物在血清和水疱液中增加。CCR6 细胞向皮肤水疱的募集呈剂量依赖性下降,在 5mg/kg 及更高剂量时出现最大效应,此时血清和水疱液中的 GSK3050002/CCL20 复合物似乎也达到了最高水平。

结论

这些结果表明 PK、靶标结合和 PD 之间存在关系,提示 GSK3050002 选择性抑制 CCR6 细胞的募集,并支持 GSK3050002 在自身免疫和炎症性疾病中的进一步开发。