Yuan D, Vitetta E S, Kettman J R
J Exp Med. 1977 Jun 1;145(6):1421-35. doi: 10.1084/jem.145.6.1421.
Murine spleen cells were depleted of specific B-cell subpopulations bearing different immunoglobulin isotypes by means of complement-mediated cytolysis after treatment with antisera specific for micron- and gamma-chains. The functional effect of this depletion was measured by assaying both the primary and secondary plaque-forming cell responses of the residual cells after transfer to carrier-primed lethally irradiated hosts. The results suggest that cells bearing IgM are the progenitors of plaque-forming cells in the primary response and cells bearing IgG are the major progenitors of IgG plaque-forming cells in the secondary response. The quantity of IgM on progenitors of secondary IgM plaque-forming cells decreases markedly as the interval between primary immunization and antigenic challenge increases. Long-term memory cells for the secondary IgM response bear small amounts of both IgM and IgG.
通过用针对μ链和γ链的抗血清处理后,借助补体介导的细胞溶解作用,去除了携带不同免疫球蛋白同种型的特定B细胞亚群的小鼠脾细胞。通过检测转移到载体致敏的致死性照射宿主后残留细胞的初次和二次空斑形成细胞反应,来测定这种去除的功能效应。结果表明,携带IgM的细胞是初次反应中空斑形成细胞的祖细胞,而携带IgG的细胞是二次反应中IgG空斑形成细胞的主要祖细胞。随着初次免疫和抗原攻击之间的间隔增加,二次IgM空斑形成细胞祖细胞上的IgM数量显著减少。二次IgM反应的长期记忆细胞同时携带少量的IgM和IgG。