Roosnek E, Lanzavecchia A
Basel Institute for Immunology, Switzerland.
J Exp Med. 1991 Feb 1;173(2):487-9. doi: 10.1084/jem.173.2.487.
Using Epstein-Barr virus B cell clones and antigen-specific T cell clones, we asked how antigen-antibody complexes are handled by B cells. We found that the only B cells capable of efficient presentation of antigen-antibody complexes are those that bind the complexes via membrane immunoglobulin, i.e., rheumatoid factor-producing B cells and, to a lower extent, antigen-specific B cells. On the contrary, nonspecific B cells, although capable of binding antigen-antibody complexes, fail to present them to T cells. Thus, rheumatoid factor B cells can present any antigen in the context of an immune complex and be triggered by T cells specific for a variety of foreign antigens. These results demonstrate a mechanism of intermolecular help that may be responsible for the production of rheumatoid factor and possibly of other types of autoantibodies.
利用爱泼斯坦-巴尔病毒B细胞克隆和抗原特异性T细胞克隆,我们探究了B细胞如何处理抗原-抗体复合物。我们发现,唯一能够有效呈递抗原-抗体复合物的B细胞是那些通过膜免疫球蛋白结合复合物的细胞,即产生类风湿因子的B细胞,以及程度较低的抗原特异性B细胞。相反,非特异性B细胞虽然能够结合抗原-抗体复合物,但无法将其呈递给T细胞。因此,类风湿因子B细胞可以在免疫复合物的背景下呈递任何抗原,并被针对多种外来抗原的T细胞触发。这些结果证明了一种分子间辅助机制,该机制可能与类风湿因子以及其他类型自身抗体的产生有关。