Ho A D, Reitter B, Stojakowits S, Fiehn W, Weisser J
Eur J Pediatr. 1980 Sep;134(3):211-6. doi: 10.1007/BF00441475.
There has been considerable interest in capping of lymphocytes in patients with Duchenne muscular dystrophy (DMD). However, the results from different authors are controversial. We have investigated cap formation in thirteen families with DMD, using a method standardized in our laboratory, and could establish diminished capping in all 12 patients and in 12 of the 13 mothers. By examining cap formation simultaneously with whole polyvalent antiserum, with F(ab)2 fragment of polyvalent antiserum, and with monospecific antisera we could also confirm this observation of defective capping in 7 patients and 4 carriers, as compared to 9 control subjects likewise examined. We have indications that treatment of the lymphocytes under unfavourable conditions e.g. preincubation in buffer solution might accentuate the decrease of lymphocyte capping in patients and carriers.
人们对杜兴氏肌营养不良症(DMD)患者淋巴细胞的帽化现象颇感兴趣。然而,不同作者的研究结果存在争议。我们采用在本实验室标准化的方法,对13个患有DMD的家庭进行了帽化形成研究,结果发现所有12名患者以及13名母亲中的12人帽化现象减弱。通过同时使用全价多克隆抗血清、多克隆抗血清的F(ab)2片段以及单特异性抗血清检测帽化形成情况,与同样接受检测的9名对照受试者相比,我们也证实了7名患者和4名携带者存在帽化缺陷的现象。我们有迹象表明,在不利条件下处理淋巴细胞,例如在缓冲溶液中预孵育,可能会加剧患者和携带者淋巴细胞帽化现象的减少。