Dattner A M, Levis W R
Dermatology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
Scand J Immunol. 1980;11(2):169-74. doi: 10.1111/j.1365-3083.1980.tb00223.x.
Stimulation of sensitive leucocyte populations with near optimal concentrations of soluble microbial antigens results in vigorous lymphocyte proliferation when 3H-thymidine incorporation is measured after 4-8 days. Lymphoblasts in these cultures revert to small lymphocytes after 10-14 days, at which time they are often refractory to any stimulant including the original incubating antigen. When these primed lymphocytes are irradiated with 500-1000 R to block their proliferation and added to fresh leucocyte culture from the same individual (autologous), they usually, but not invariably, reduce the proliferation of the unirradiated fresh leucocyte cultures. Exposure to 6000 R reduced the suppressor activity. Reduction was specific for the microbial antigen with which they were originally generated, but, more often, a combination of both specific and nonspecific suppression was observed. These data provide good evidence, with reciprocal specificity, for the generation of antigen specific suppression in vitro.
用接近最佳浓度的可溶性微生物抗原刺激敏感白细胞群体,在4 - 8天后测量³H - 胸苷掺入量时,会导致淋巴细胞剧烈增殖。这些培养物中的淋巴母细胞在10 - 14天后会恢复为小淋巴细胞,此时它们通常对任何刺激物(包括最初孵育的抗原)都不敏感。当这些致敏淋巴细胞接受500 - 1000伦琴的照射以阻断其增殖,并添加到来自同一个体(自体)的新鲜白细胞培养物中时,它们通常(但并非总是)会降低未照射的新鲜白细胞培养物的增殖。暴露于6000伦琴会降低抑制活性。这种降低对最初产生它们的微生物抗原具有特异性,但更常见的是,会观察到特异性和非特异性抑制的组合。这些数据以相互特异性为体外产生抗原特异性抑制提供了有力证据。