Baker P J, Stashak P W, Amsbaugh D F, Prescott B
Immunology. 1971 Apr;20(4):481-92.
A procedure based on the rate of appearance of plaque-forming cells (PFC) in agarose was used to measure the relative rates of antibody synthesis and release by cells making antibody specific for Type III pneumococcal polysaccharide (SSS-III). The rate of antibody synthesis and release by SSS-III-specific PFC was directly related to the immunizing dose employed; maximal values were obtained with mice given an optimally immunogenic dose (0.5 μg) of SSS-III. However, dose-dependent reductions, not only in the magnitude of the antibody response, but also in the rate of antibody synthesis and release by specific PFC, were noted in mice receiving doses greater than 0.5 μg. The latter suggests that a decrease in the rate of antibody synthesis and release by antibody-forming cells may be an initial step in the induction of immunological paralysis by high doses of SSS-III. Increases in the magnitude of the serum antibody and the PFC response were associated with corresponding increases in the rate of antibody synthesis and release by SSS-III-specific PFC following immunization; this suggests that cell differentiation—rather than proliferation—plays a major rôle in the development of the antibody response to SSS-III. In contrast, the results obtained in similar studies with sheep erythrocytes indicate that cell proliferation influences to a greater degree the magnitude of the antibody response elicited to this antigen.
一种基于琼脂糖中噬斑形成细胞(PFC)出现速率的方法,被用于测量产生针对Ⅲ型肺炎球菌多糖(SSS-III)特异性抗体的细胞合成和释放抗体的相对速率。SSS-III特异性PFC合成和释放抗体的速率与所采用的免疫剂量直接相关;给小鼠注射最佳免疫原剂量(0.5μg)的SSS-III可获得最大值。然而,在接受大于0.5μg剂量的小鼠中,不仅抗体反应的强度出现剂量依赖性降低,而且特异性PFC合成和释放抗体的速率也降低。后者表明,抗体形成细胞合成和释放抗体速率的降低可能是高剂量SSS-III诱导免疫麻痹的初始步骤。免疫后,血清抗体和PFC反应强度的增加与SSS-III特异性PFC合成和释放抗体速率的相应增加相关;这表明细胞分化而非增殖在对SSS-III的抗体反应发展中起主要作用。相比之下,在对绵羊红细胞进行的类似研究中获得的结果表明,细胞增殖对该抗原引发的抗体反应强度影响更大。