Ehl S, Nuesch R, Tanaka T, Myasaka M, Hengartner H, Zinkernagel R
Division of Bioregulation, Biomedical Research Center, Osaka University Medical Center, Suita, Japan.
J Immunol Methods. 1996 Dec 15;199(2):149-53. doi: 10.1016/s0022-1759(96)00175-5.
This study compares in vivo efficacy and specificity of the three NK cell depleting antibodies anti-asialo GM1, anti-NK 1.1 and the recently described TM beta 1, which is directed against the interleukin-2 receptor beta chain. All three antibodies are equally efficacious as assessed by abolishing NK mediated cytolytic activity induced by a high dose virus infection or Poly IC against YAC-1 targets. Similarly, the generation of virus-specific cytotoxic T cells (CTL) was unimpaired after NK depletion in two different virus infections. However, if mice are treated with the antibodies several days after virus infection, when strong CTL responses have already been generated, anti-asialo GM1 and-to a lesser extent-also TM beta 1 have a significant effect on CTL activity. Only after treatment with anti-NK 1.1 antibody, CTL activity was not significantly impaired. We conclude, that of the NK depleting antibodies currently available, anti-NK 1.1 allows the best differentiation of activated CTL and NK cells in vivo.
本研究比较了三种NK细胞耗竭抗体抗去唾液酸GM1、抗NK 1.1和最近描述的针对白细胞介素-2受体β链的TMβ1的体内疗效和特异性。通过消除高剂量病毒感染或聚肌胞苷酸(Poly IC)诱导的针对YAC-1靶标的NK介导的溶细胞活性评估,所有三种抗体的疗效相同。同样,在两种不同的病毒感染中,NK细胞耗竭后病毒特异性细胞毒性T细胞(CTL)的产生未受损害。然而,如果在病毒感染数天后用这些抗体治疗小鼠,此时已经产生了强烈的CTL反应,抗去唾液酸GM1以及在较小程度上TMβ1对CTL活性有显著影响。只有在用抗NK 1.1抗体治疗后,CTL活性才没有受到显著损害。我们得出结论,在目前可用的NK细胞耗竭抗体中,抗NK 1.1在体内对活化的CTL和NK细胞具有最佳的区分能力。