Ezine S, Papiernik M, Rieger F, Pinçon-Raymond M
Clin Exp Immunol. 1983 Mar;51(3):475-8.
Motor end-plate disease (Med) in mice is associated with complex immunological abnormalities which are shared by the heterozygous +/MedJ mice, which exhibit no or mild clinical manifestations, and by MedJ/MedJ mice which die from this neuromuscular disorder. In the present paper we extend our immunological data with the study of splenic lymphocyte subsets with Lyt monoclonal antibodies. Both MedJ/MedJ and +/MedJ 14-18 day old mice have high Lyt1+/Lyt2+ ratios, with higher Lyt1+ and reduced Lyt2+ lymphocyte pools as compared to normal mice. This correlates with the low suppressive function previously described, but is unexpected in view of the low helper function as measured by the response to SRBC immunization. Adult +/MedJ mice recovered normal T lymphocyte subset levels, while the small group of MedJ/MedJ mice that escapes death but continues to suffer from the neuromuscular illness maintains high Lyt1+/Lyt2+ ratios.
小鼠的运动终板病(Med)与复杂的免疫异常有关,杂合子+/MedJ小鼠(无或仅有轻微临床表现)以及因这种神经肌肉疾病死亡的MedJ/MedJ小鼠都存在这种免疫异常。在本文中,我们通过用Lyt单克隆抗体研究脾淋巴细胞亚群来扩展我们的免疫学数据。14 - 18日龄的MedJ/MedJ和+/MedJ小鼠均具有较高的Lyt1+/Lyt2+比值,与正常小鼠相比,Lyt1+淋巴细胞池增加,Lyt2+淋巴细胞池减少。这与先前描述的低抑制功能相关,但鉴于对SRBC免疫反应所测得的低辅助功能,这一结果出乎意料。成年+/MedJ小鼠的T淋巴细胞亚群水平恢复正常,而一小部分逃脱死亡但仍患有神经肌肉疾病的MedJ/MedJ小鼠维持着较高的Lyt1+/Lyt2+比值。