Esmon N L, Little J R
J Immunol. 1976 Sep;117(3):919-26.
An indirect radioimmunoassay has been used to study the antibody-induced changes in expression of TL antigens on mouse thymus and leukemia cells. The results obtained indicate that the incubation of TL+ cells in relatively high concentrations of anti-TL antisera results in a detectable, but not major, loss in the quantity of antigen detected in the plasma membranes. This decrease is not inhibited by azide. Although the antigen loss seems to coincide with the appearance of patching of membrane TL antigens on leukemia cells observed in indirect immunofluorescence microscopy, this is not the case when thymocytes are used as targets. Fab fragments prepared from anti-TL antibodies can also induce a quantitative decrease in antigen expression. The major mechanism involved in membrane antigen loss seems to be endocytosis, although some shedding may also occur. Resistance to immune cytolysis (antigenic modulation) occurs during incubation in anti-TL antibodies before either endocytosis or antigen redistribution has progressed enough to be directly responsible. Since antigenic modulation does not represent a depletion in TL antigens being expressed on the cell surfaces, another mechanism must account for the failure of guinea pig complement to achieve cell lysis.
一种间接放射免疫测定法已被用于研究抗体诱导的小鼠胸腺和白血病细胞上TL抗原表达的变化。所获得的结果表明,将TL+细胞在相对高浓度的抗TL抗血清中孵育会导致在质膜中检测到的抗原量出现可检测但并非主要的损失。这种减少不受叠氮化物的抑制。尽管抗原损失似乎与在间接免疫荧光显微镜下观察到的白血病细胞膜TL抗原的斑块形成同时出现,但以胸腺细胞作为靶细胞时情况并非如此。从抗TL抗体制备的Fab片段也可诱导抗原表达的定量减少。膜抗原损失所涉及的主要机制似乎是内吞作用,尽管也可能发生一些脱落。在抗TL抗体孵育期间,在内吞作用或抗原重新分布进展到足以直接导致免疫细胞溶解(抗原调制)失败之前,就出现了对免疫细胞溶解的抗性。由于抗原调制并不代表细胞表面表达的TL抗原的消耗,所以必须有另一种机制来解释豚鼠补体无法实现细胞裂解的原因。