Gras J, Tilló T
Ann Immunol (Paris). 1981 Mar-Apr;132C(2):145-55. doi: 10.1016/0769-2625(81)90023-4.
Using the mouse PFC anti-SRBC response, the temporal relationship between primary antigen dose and cyclophosphamide (CP) administration necessary for the inhibition of priming for the secondary IgG response was studied. The administration of CP 1 h after the primary or secondary antigen injection inhibits the responses in both cases. The administration of CP 1 h after the primary antigen injection does not inhibit priming for the secondary response; this priming is inhibited if CP is administered at 12 h or more, and the maximal degree of inhibition is induced when CP is administered 7 or 9 days after the primary antigen injection. Therefore, the proliferation stage of mature B cells to IgM secretion is not necessary for this priming. It is suggested that the switch from IgM to IgG takes place in a proliferative stage of B-cell precursors in presence of the antigen.
利用小鼠PFC抗SRBC反应,研究了抑制二次IgG反应启动所需的初次抗原剂量与环磷酰胺(CP)给药之间的时间关系。在初次或二次抗原注射后1小时给予CP,在两种情况下均会抑制反应。在初次抗原注射后1小时给予CP不会抑制二次反应的启动;如果在12小时或更长时间给予CP,则这种启动会受到抑制,并且在初次抗原注射后7或9天给予CP时会诱导出最大程度的抑制。因此,成熟B细胞增殖至分泌IgM的阶段对于这种启动不是必需的。有人提出,在抗原存在的情况下,B细胞前体的增殖阶段会发生从IgM到IgG的转换。