Yu X Z, Anasetti C
Division of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.
Transplantation. 2000 Jan 15;69(1):104-12. doi: 10.1097/00007890-200001150-00019.
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.
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.
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.
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.
抗CD3ε F(ab')2对初始T细胞无促有丝分裂作用,但在体外和体内均可诱导抗原激活的T细胞凋亡。我们研究了无促有丝分裂作用的抗CD3ε F(ab')2抗体诱导T细胞死亡的机制。
通过体内免疫和体外再刺激产生卵清蛋白反应性T细胞系。用特异性单克隆抗体进行表面染色检测Fas或Fas配体(FasL)的表达。用碘化丙啶染色DNA检测凋亡DNA和细胞周期阶段。用ELISA法检测干扰素-γ,用生物测定法检测白细胞介素(IL)-2和IL-4。
用抗CD3ε F(ab')2再刺激可诱导抗原激活的野生型T细胞凋亡,但不能诱导Fas或FasL缺陷的T细胞凋亡。抗CD3ε F(ab')2可诱导表达高水平Fas和FasL的细胞死亡,优先清除辅助性T细胞(Th)1细胞,而保留Th2细胞。可溶性抗CD3ε F(ab')2不调节Fas或诱导FasL表达,表明抗CD3ε F(ab')2诱导T细胞凋亡的能力依赖于一种独特的机制。发现处于S/G2期的T细胞对Fas介导的凋亡相对抗性,但抗CD3ε F(ab')2使这些T细胞对Fas介导的凋亡极为敏感。
抗CD3ε F(ab')2通过激活Fas/FasL途径诱导循环中的CD4+ T细胞凋亡。抗CD3ε F(ab')2不调节Fas或FasL表达,但诱导循环T细胞对Fas介导的凋亡敏感。抗CD3ε F(ab')2可诱导极化的Th1细胞死亡,但不能诱导Th2细胞死亡,因此可能使抗原激活的T细胞库向Th2表型倾斜。这些特征预示,无促有丝分裂作用的抗CD3ε F(ab')2样抗体可用于预防或逆转由Th1细胞介导的致病性免疫反应。