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用于牛白血病病毒感染牛免疫治疗的抗牛程序性死亡1大鼠-牛嵌合抗体

Anti-Bovine Programmed Death-1 Rat-Bovine Chimeric Antibody for Immunotherapy of Bovine Leukemia Virus Infection in Cattle.

作者信息

Okagawa Tomohiro, Konnai Satoru, Nishimori Asami, Maekawa Naoya, Ikebuchi Ryoyo, Goto Shinya, Nakajima Chie, Kohara Junko, Ogasawara Satoshi, Kato Yukinari, Suzuki Yasuhiko, Murata Shiro, Ohashi Kazuhiko

机构信息

Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan.

Division of Bioresources, Research Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.

出版信息

Front Immunol. 2017 Jun 7;8:650. doi: 10.3389/fimmu.2017.00650. eCollection 2017.

Abstract

Blockade of immunoinhibitory molecules, such as programmed death-1 (PD-1)/PD-ligand 1 (PD-L1), is a promising strategy for reinvigorating exhausted T cells and preventing disease progression in a variety of chronic infections. Application of this therapeutic strategy to cattle requires bovinized chimeric antibody targeting immunoinhibitory molecules. In this study, anti-bovine PD-1 rat-bovine chimeric monoclonal antibody 5D2 (Boch5D2) was constructed with mammalian expression systems, and its biochemical function and antiviral effect were characterized and using cattle infected with bovine leukemia virus (BLV). Purified Boch5D2 was capable of detecting bovine PD-1 molecules expressed on cell membranes in flow cytometric analysis. In particular, Biacore analysis determined that the binding affinity of Boch5D2 to bovine PD-1 protein was similar to that of the original anti-bovine PD-1 rat monoclonal antibody 5D2. Boch5D2 was also capable of blocking PD-1/PD-L1 binding at the same level as 5D2. The immunomodulatory and therapeutic effects of Boch5D2 were evaluated by administration of the antibody to a BLV-infected calf. Inoculated Boch5D2 was sustained in the serum for a longer period. Boch5D2 inoculation resulted in activation of the proliferation of BLV-specific CD4 T cells and decrease in the proviral load of BLV in the peripheral blood. This study demonstrates that Boch5D2 retains an equivalent biochemical function to that of the original antibody 5D2 and is a candidate therapeutic agent for regulating antiviral immune response . Clinical efficacy of PD-1/PD-L1 blockade awaits further experimentation with a large number of animals.

摘要

阻断免疫抑制分子,如程序性死亡受体 1(PD-1)/程序性死亡受体配体 1(PD-L1),是恢复耗竭 T 细胞活力并预防多种慢性感染中疾病进展的一种有前景的策略。将这种治疗策略应用于牛需要针对免疫抑制分子的牛源化嵌合抗体。在本研究中,使用哺乳动物表达系统构建了抗牛 PD-1 大鼠-牛嵌合单克隆抗体 5D2(Boch5D2),并利用感染牛白血病病毒(BLV)的牛对其生化功能和抗病毒效果进行了表征。在流式细胞术分析中,纯化的 Boch5D2 能够检测细胞膜上表达的牛 PD-1 分子。特别是,Biacore 分析确定 Boch5D2 与牛 PD-1 蛋白的结合亲和力与原始抗牛 PD-1 大鼠单克隆抗体 5D2 相似。Boch5D2 也能够以与 5D2 相同的水平阻断 PD-1/PD-L1 结合。通过向感染 BLV 的小牛施用该抗体来评估 Boch5D2 的免疫调节和治疗效果。接种的 Boch5D2 在血清中持续存在的时间更长。接种 Boch5D2 导致 BLV 特异性 CD4 T 细胞增殖活化,并降低外周血中 BLV 的前病毒载量。本研究表明,Boch5D2 保留了与原始抗体 5D2 相当的生化功能,是调节抗病毒免疫反应的候选治疗剂。PD-1/PD-L1 阻断的临床疗效有待大量动物的进一步实验验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7de1/5461298/e6605d2153a6/fimmu-08-00650-g001.jpg

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