Fuleihan R, Ramesh N, Loh R, Jabara H, Rosen R S, Chatila T, Fu S M, Stamenkovic I, Geha R S
Division of Immunology, Children's Hospital, Boston, MA.
Proc Natl Acad Sci U S A. 1993 Mar 15;90(6):2170-3. doi: 10.1073/pnas.90.6.2170.
B lymphocytes from patients with X chromosome-linked immunoglobulin deficiency with normal or elevated serum IgM are unable to switch from the synthesis of IgM/IgD to that of other immunoglobulin isotypes. Isotype switch recombination was evaluated in three affected males by examining interleukin 4-driven IgE synthesis. T-cell-dependent IgE synthesis was completely absent in the B lymphocytes of the patients. In contrast, CD40 mAb plus interleukin 4 induced the patients' B cells to synthesize IgE and to undergo deletional switch recombination. Because interaction between CD40 and its ligand on activated T cells is critical for T-cell-driven isotype switching, we examined CD40 ligand expression. In contrast to normal T cells, lymphocytes from the patients expressed no detectable CD40 ligand on their surface after stimulation with phorbol 12-myristate 13-acetate and ionomycin, although the mRNA of the ligand was expressed normally. These results suggest that defective expression of the CD40 ligand underlies the failure of isotype switching in this disease.
患有X染色体连锁免疫球蛋白缺陷且血清IgM正常或升高的患者的B淋巴细胞无法从IgM/IgD的合成转换为其他免疫球蛋白同种型的合成。通过检测白细胞介素4驱动的IgE合成,对三名受影响男性的同种型转换重组进行了评估。患者的B淋巴细胞中完全不存在T细胞依赖性IgE合成。相比之下,CD40单克隆抗体加白细胞介素4诱导患者的B细胞合成IgE并进行缺失性转换重组。由于CD40与其在活化T细胞上的配体之间的相互作用对于T细胞驱动的同种型转换至关重要,我们检测了CD40配体的表达。与正常T细胞相比,患者的淋巴细胞在用佛波醇12-肉豆蔻酸酯13-乙酸酯和离子霉素刺激后,其表面未检测到可检测到的CD40配体,尽管配体的mRNA正常表达。这些结果表明,CD40配体的缺陷表达是该疾病中同种型转换失败的基础。