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在小鼠中,通过环孢素A治疗预防抗T细胞受体αβ单克隆抗体诱导的副作用,而不干扰单克隆抗体诱导的免疫抑制。

Prevention of anti-T-cell receptor alpha beta monoclonal antibody-induced side-effects by treatment with cyclosporin A without interference of monoclonal antibody-induced immunosuppression in mice.

作者信息

Murakami Y, Kong Y Y, Nishimura Y, Nomoto K, Umesue M, Omoto K, Maeda T, Nomoto K

机构信息

Department of Immunology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.

出版信息

Immunology. 1995 Oct;86(2):238-43.

Abstract

Anti-T-cell receptor (TCR)alpha beta monoclonal antibody (mAb; H57-597) injection in mice caused cytokine (tumour necrosis factor and interferon-gamma) release and clinical side-effects such as piloerection and body weight loss similar to anti-CD3 mAb (145-2C11) injection. Treatment with cyclosporin A (CsA) for 3 days, from day -2 to day 0, prior to anti-TCR alpha beta mAb injection almost completely abolished the mAb-induced cytokine release, and completely inhibited the mAb-induced body weight loss. Furthermore, treatment with CsA from day -2 to day 0 did not inhibit the mAb-induced in vivo immunosuppressive effects, i.e. prolongation of skin allograft and T-cell depletion in the periphery. These results indicate that CsA treatment prior to mAb treatment could effectively inhibit the mAb-induced side-effects without interference of the mAb-induced in vivo immunosuppression. From these results, we propose that CsA treatment prior to injection of anti-TCR alpha beta mAb may be recommended to reduce mAb-induced side-effects.

摘要

在小鼠中注射抗T细胞受体(TCR)αβ单克隆抗体(mAb;H57-597)会导致细胞因子(肿瘤坏死因子和干扰素-γ)释放以及出现诸如竖毛和体重减轻等临床副作用,这与注射抗CD3 mAb(145-2C11)类似。在抗TCRαβ mAb注射前从第-2天至第0天用环孢素A(CsA)治疗3天,几乎完全消除了mAb诱导的细胞因子释放,并完全抑制了mAb诱导的体重减轻。此外,从第-2天至第0天用CsA治疗并未抑制mAb诱导的体内免疫抑制作用,即皮肤同种异体移植的延长和外周T细胞的耗竭。这些结果表明,在mAb治疗前进行CsA治疗可有效抑制mAb诱导的副作用,而不会干扰mAb诱导的体内免疫抑制作用。基于这些结果,我们建议在注射抗TCRαβ mAb前进行CsA治疗,以减少mAb诱导的副作用。

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