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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Enhancement of susceptibility to Fas-mediated apoptosis of TH1 cells by nonmitogenic anti-CD3epsilon F(ab')2.
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Enhancement of susceptibility to Fas-mediated apoptosis of TH1 cells by nonmitogenic anti-CD3epsilon F(ab')2.

机译:非有丝分裂的抗CD3epsilon F(ab')2对Fas介导的TH1细胞凋亡的敏感性增强。

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BACKGROUND: Anti-CD3epsilon F(ab')2 are nonmitogenic for naive T cells but can induce apoptosis of antigen-activated T cells in vitro and in vivo. We studied the mechanisms by which nonmitogenic anti-CD3epsilon F(ab')2 antibodies induce T cell death. METHODS: OVA-responsive T cell lines were generated by immunization in vivo and restimulation in vitro. Fas or Fas ligand (FasL) expression was tested by surface staining with specific mAbs. The apoptotic DNA and cell cycle phase were tested by staining DNA with propidium iodide. Interferon-gamma was measured by ELISA, whereas interleukin (IL)-2 and IL-4 were detected by bioassays. RESULTS: Restimulation with anti-CD3epsilon F(ab')2 induced apoptosis of antigen-activated wild-type T cells, but not Fas or FasL-defective T cells. Anti-CD3epsilon F(ab')2 induced death of cells expressing high levels of Fas and FasL, and preferentially deleted T helper (Th)1 cells but spared Th2 cells. Soluble anti-CD3epsilon F(ab')2 did not regulate Fas or induce FasL expression, indicating that the ability of anti-CD3epsilon F(ab')2 to induce T cell apoptosis depends on a distinct mechanism. T cells in S/G2 were found relatively resistant to Fas-mediated apoptosis, but anti-CD3epsilon F(ab')2 rendered those T cells exquisitely sensitive to Fas-mediated apoptosis. CONCLUSIONS: Anti-CD3epsilon F(ab')2 induces apoptosis of cycling CD4+ T cells through activation of the Fas/FasL pathway. Anti-CD3epsilon F(ab')2 does not regulate Fas or FasL expression but induces susceptibility to Fas-mediated apoptosis of cycling T cells. Anti-CD3epsilon F(ab')2 can induce death of polarized Th1 cells, but not Th2 cells, thus potentially skewing the repertoire of antigen-activated T cells toward the Th2 phenotype. These features predict that nonmitogenic anti-CD3epsilon F(ab')2-like antibodies can be useful to prevent or reverse pathogenic immune responses mediated by Th1 cells.
机译:背景:抗CD3epsilon F(ab')2对幼稚T细胞无促有丝分裂作用,但可在体内和体外诱导抗原激活的T细胞凋亡。我们研究了非促有丝分裂的抗CD3epsilon F(ab')2抗体诱导T细胞死亡的机制。方法:通过体内免疫和体外再刺激产生OVA反应性T细胞系。 Fas或Fas配体(FasL)的表达通过用特异性mAb进行表面染色来测试。通过用碘化丙啶染色DNA来测试凋亡DNA和细胞周期阶段。干扰素-γ通过ELISA测定,而白介素(IL)-2和IL-4通过生物测定法检测。结果:用抗CD3epsilon F(ab')2重新刺激可诱导抗原激活的野生型T细胞凋亡,但不会引起Fas或FasL缺陷型T细胞凋亡。抗CD3epsilon F(ab')2诱导表达高水平Fas和FasL的细胞死亡,并优先删除T辅助(Th)1细胞,但保留Th2细胞。可溶性抗CD3epsilon F(ab')2不能调节Fas或诱导FasL表达,表明抗CD3epsilon F(ab')2诱导T细胞凋亡的能力取决于不同的机制。 S / G2中的T细胞被发现对Fas介导的细胞凋亡具有相对抗性,但抗CD3epsilon F(ab')2使这些T细胞对Fas介导的细胞凋亡极为敏感。结论:抗CD3epsilon F(ab')2通过激活Fas / FasL途径诱导循环CD4 + T细胞凋亡。抗CD3epsilon F(ab')2不调节Fas或FasL的表达,但诱导对Fas介导的循环性T细胞凋亡的敏感性。抗CD3epsilon F(ab')2可以诱导极化的Th1细胞死亡,但不会诱导Th2细胞死亡,因此可能会使抗原激活的T细胞的组成向Th2表型倾斜。这些特征预测,非促有丝分裂的抗CD3epsilon F(ab')2样抗体可用于预防或逆转Th1细胞介导的病原性免疫应答。

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