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抗猫肿瘤坏死因子-α小鼠-猫嵌合抗体的研制。

Development of a mouse-feline chimeric antibody against feline tumor necrosis factor-alpha.

作者信息

Doki Tomoyoshi, Takano Tomomi, Hohdatsu Tsutomu

机构信息

Laboratory of Veterinary Infectious Disease, School of Veterinary Medicine, Kitasato University, Towada, Aomori 034-8628, Japan.

出版信息

J Vet Med Sci. 2016 Oct 1;78(9):1447-1455. doi: 10.1292/jvms.16-0020. Epub 2016 Jun 4.

Abstract

Feline infectious peritonitis (FIP) is a fatal inflammatory disease caused by FIP virus infection. Feline tumor necrosis factor (fTNF)-alpha is closely involved in the aggravation of FIP pathology. We previously described the preparation of neutralizing mouse anti-fTNF-alpha monoclonal antibody (mAb 2-4) and clarified its role in the clinical condition of cats with FIP using in vitro systems. However, administration of mouse mAb 2-4 to cat may lead to a production of feline anti-mouse antibodies. In the present study, we prepared a mouse-feline chimeric mAb (chimeric mAb 2-4) by fusing the variable region of mouse mAb 2-4 to the constant region of feline antibody. The chimeric mAb 2-4 was confirmed to have fTNF-alpha neutralization activity. Purified mouse mAb 2-4 and chimeric mAb 2-4 were repeatedly administered to cats, and the changes in the ability to induce feline anti-mouse antibody response were investigated. In the serum of cats treated with mouse mAb 2-4, feline anti-mouse antibody production was induced, and the fTNF-alpha neutralization effect of mouse mAb 2-4 was reduced. In contrast, in cats treated with chimeric mAb 2-4, the feline anti-mouse antibody response was decreased compared to that of mouse mAb 2-4-treated cats.

摘要

猫传染性腹膜炎(FIP)是一种由FIP病毒感染引起的致命性炎症性疾病。猫肿瘤坏死因子(fTNF)-α与FIP病理的加重密切相关。我们之前描述了中和性小鼠抗fTNF-α单克隆抗体(mAb 2-4)的制备,并使用体外系统阐明了其在患有FIP的猫的临床状况中的作用。然而,将小鼠mAb 2-4给予猫可能会导致猫产生抗小鼠抗体。在本研究中,我们通过将小鼠mAb 2-4的可变区与猫抗体的恒定区融合,制备了一种小鼠-猫嵌合单克隆抗体(嵌合mAb 2-4)。证实嵌合mAb 2-4具有fTNF-α中和活性。将纯化的小鼠mAb 2-4和嵌合mAb 2-4反复给予猫,并研究诱导猫抗小鼠抗体反应能力的变化。在用小鼠mAb 2-4治疗的猫的血清中,诱导产生了猫抗小鼠抗体,并且小鼠mAb 2-4的fTNF-α中和作用降低。相比之下,在用嵌合mAb 2-4治疗的猫中,与用小鼠mAb 2-4治疗的猫相比,猫抗小鼠抗体反应有所降低。

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