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初次注射与环磷酰胺给药之间的时间关系对于抑制二次反应的启动是必要的。

Temporal relationship between primary injection and cyclophosphamide administration necessary for the inhibition of the priming for a secondary response.

作者信息

Gras J, Tilló T

出版信息

Ann Immunol (Paris). 1981 Mar-Apr;132C(2):145-55. doi: 10.1016/0769-2625(81)90023-4.

Abstract

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.

摘要

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。

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