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大鼠肝脏诱导的自发耐受诱导期细胞毒性T细胞的CD4 T细胞调节

CD4 T-cell regulation of cytotoxic T cells during the induction phase of liver-induced spontaneous tolerance in rats.

作者信息

Ishii Tatsuhiro, Yamaguchi Junzo, Gu Weili, Hashimoto Toshiaki, Yamamoto Takao, Kanematsu Takashi

机构信息

Department of Surgery II, Nagasaki University School of Medicine, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.

出版信息

Surg Today. 2005;35(6):473-9. doi: 10.1007/s00595-004-2964-5.

Abstract

PURPOSE

To check for in vivo CD4 T-cell-mediated inhibition of the immune response in rats with spontaneously accepted liver transplants.

METHODS

Using the Lewis to Wistar Furth rat strain combination, we performed transient in vivo depletion of CD4 T-cells by anti-CD4 monoclonal antibodies (mAb) after liver transplantation. We used the CTL assay to detect primed T cells. We also retransplanted a grafted donor liver, parked for 3 days, into a secondary naive recipient rat.

RESULTS

When Lewis rat livers were transplanted into the recipient Wistar Furth rats, the grafts suffered an early immune attack, followed by spontaneous acceptance without immunosuppression. However, giving anti-CD4 mAb to the recipients at the time of grafting prolonged the acute rejection reaction. Furthermore, giving anti-CD4 therapy on postoperative days (PODs) 21 and 35, but not on PODs 56 and 100, induced transient liver damage in recipients overcoming acute rejection. No primed T cells were detected by the CTL assay in the recipient rats within 2 months after transplantation. Meanwhile, the retransplanted liver had no ability to elicit an immune attack.

CONCLUSIONS

CD4 T cells seemed to downregulate the effector function of T cells, but not T-cell proliferation in this model.

摘要

目的

检测在自发接受肝移植的大鼠体内,CD4 T细胞对免疫反应的介导抑制作用。

方法

利用Lewis大鼠与Wistar Furth大鼠的品系组合,在肝移植后通过抗CD4单克隆抗体(mAb)对CD4 T细胞进行体内短暂清除。我们使用细胞毒性T淋巴细胞(CTL)检测法来检测致敏T细胞。我们还将移植后停放3天的供体肝脏再次移植到第二只未经致敏的受体大鼠体内。

结果

当将Lewis大鼠的肝脏移植到受体Wistar Furth大鼠体内时,移植物遭受早期免疫攻击,随后在无免疫抑制的情况下自发被接受。然而,在移植时给受体注射抗CD4 mAb会延长急性排斥反应。此外,在术后第21天和第35天给予抗CD4治疗,但在第56天和第100天不给予,会在克服急性排斥反应的受体中诱导短暂性肝损伤。移植后2个月内,在受体大鼠中通过CTL检测法未检测到致敏T细胞。同时,再次移植的肝脏没有引发免疫攻击的能力。

结论

在该模型中,CD4 T细胞似乎下调了T细胞的效应功能,但未下调T细胞增殖。

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