Lang J, Jackson M, Teyton L, Brunmark A, Kane K, Nemazee D
Department of Immunology, University of Colorado Health Sciences Center, Denver 80220, USA.
J Exp Med. 1996 Nov 1;184(5):1685-97. doi: 10.1084/jem.184.5.1685.
To assess the sensitivity of B cell tolerance with respect to receptor/autoantigen affinity, we identified low affinity ligands to the 3-83 (anti-major histocompatibility complex class I) antibody and tested the ability of these ligands to induce central and peripheral tolerance in 3-83 transgenic mice. Several class I protein alloforms, including Kbm3 and Dk, showed remarkably low, but detectable, affinity to 3-83. The 3-83 antibody bound Kb with K lambda approximately 2 x 10(5) M-1 and bound 10-fold more weakly to the Kbm3 (K lambda approximately 2 x 10(4) M-1) and Dk antigens. Breeding 3-83 immunoglobulin transgenic mice with mice expressing these ultralow affinity Kbm3 and Dk ligands resulted in virtually complete deletion of the autoreactive B cells from the peripheral lymphoid tissues. These low affinity antigens also induced receptor editing, as measured by elevated RAG mRNA levels in the bone marrow and excess levels of id- variant B cells bearing lambda light chains in the spleen. Reactive class I antigens were also able to mediate deletion of mature B cells when injected into the peritoneal cavity of 3-83 transgenic mice. Although the highest affinity ligand, Kk, was consistently able to induce elimination of the 3-83 peritoneal B cells, the lower affinity ligands were only partially effective. These results demonstrate the remarkable sensitivity of the deletion and receptor-editing mechanisms in immature B cells, and may suggest a higher affinity threshold for deletion of peripheral, mature B cells.
为了评估B细胞耐受性对受体/自身抗原亲和力的敏感性,我们鉴定了针对3-83(抗主要组织相容性复合体I类)抗体的低亲和力配体,并测试了这些配体在3-83转基因小鼠中诱导中枢和外周耐受性的能力。几种I类蛋白质同种型,包括Kbm3和Dk,对3-83显示出极低但可检测到的亲和力。3-83抗体与Kb的结合常数Kλ约为2×10⁵ M⁻¹,与Kbm3(Kλ约为2×10⁴ M⁻¹)和Dk抗原的结合弱10倍。将3-83免疫球蛋白转基因小鼠与表达这些超低亲和力Kbm3和Dk配体的小鼠杂交,导致外周淋巴组织中自身反应性B细胞几乎完全缺失。这些低亲和力抗原还诱导了受体编辑,这通过骨髓中RAG mRNA水平升高以及脾脏中携带λ轻链的独特型变异B细胞水平过高来衡量。当将反应性I类抗原注射到3-83转基因小鼠的腹腔中时,它们也能够介导成熟B细胞的缺失。尽管最高亲和力配体Kk始终能够诱导3-83腹腔B细胞的清除,但较低亲和力配体仅部分有效。这些结果证明了未成熟B细胞中缺失和受体编辑机制的显著敏感性,并可能提示外周成熟B细胞缺失存在更高的亲和力阈值。