Finkelman F D, Holmes J M, Dukhanina O I, Morris S C
Department of Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814.
J Exp Med. 1995 Feb 1;181(2):515-25. doi: 10.1084/jem.181.2.515.
In vivo experiments were performed to determine whether the cross-linking of membrane immunoglobulin (mIg) D on mature B cells, in the absence of T cell help, leads to B cell death. Mice were injected with either a monoclonal antibody (mAb) that cross-links mIgD effectively or a mAb that binds to mIgD avidly but cross-links it to a limited extent, and effects on B cell number and B cell Ia, mIgM, and mIgD expression were observed. In most experiments, mice were pretreated with anti-interleukin 7 mAb to prevent the generation of new bone marrow B cells, and with anti-CD4 mAb to prevent the generation of T cell help. In some experiments, mice also received anti-Fc gamma RII mAb to prevent cross-linking of mIgD with Fc gamma RII, and cobra venom factor to prevent possible mIg-complement receptor interactions and complement-mediated killing of B cells. The results of these studies demonstrate that (a) even limited cross-linking of mIgD on mature B cells can lead to B cell death; (b) increased cross-linking of mIgD leads to increased B cell death; (c) the loss of B cells is first detected 2 d after anti-IgD mAb injection and increases during the subsequent 3 d; (d) sustained modulation of mIgD may be necessary to cause B cell death; (e) mIgMdull but not mIgMbright B cells are lost in mice injected with anti-IgD mAbs; and (f) T cell help prevents or minimizes B cell death.
进行体内实验以确定在没有T细胞辅助的情况下,成熟B细胞上膜免疫球蛋白(mIg)D的交联是否会导致B细胞死亡。给小鼠注射能有效交联mIgD的单克隆抗体(mAb)或能强烈结合mIgD但交联程度有限的mAb,并观察对B细胞数量以及B细胞Ia、mIgM和mIgD表达的影响。在大多数实验中,用抗白细胞介素7 mAb预处理小鼠以防止新的骨髓B细胞生成,并用抗CD4 mAb防止T细胞辅助的产生。在一些实验中,小鼠还接受抗FcγRII mAb以防止mIgD与FcγRII交联,以及眼镜蛇毒因子以防止可能的mIg - 补体受体相互作用和补体介导的B细胞杀伤。这些研究结果表明:(a)即使成熟B细胞上mIgD的交联有限也可导致B细胞死亡;(b)mIgD交联增加导致B细胞死亡增加;(c)抗IgD mAb注射后2天首次检测到B细胞丢失,并在随后3天内增加;(d)可能需要持续调节mIgD才能导致B细胞死亡;(e)在注射抗IgD mAb的小鼠中,mIgMdull而非mIgMbright B细胞会丢失;以及(f)T细胞辅助可预防或最小化B细胞死亡。