Ron Y, De Baetselier P, Gordon J, Feldman M, Segal S
Eur J Immunol. 1981 Dec;11(12):964-8. doi: 10.1002/eji.1830111203.
Mice were injected from day of birth onward with rabbit anti-mouse IgM antiserum or purified rabbit anti-mouse IgM antibodies. These mice completely lacked Ig-positive cells or serum Ig, as analyzed by specific fluoresceinated antibodies on the fluorescence-activated cell sorter (FACS-II), by polyclonal B cell mitogens and by specific precipitation in agar. These animals were then primed in vivo by antigen emulsified in complete Freund's adjuvant, and, subsequently, their draining lymph nodes were tested for their T cell proliferative responses in vitro, to the relevant antigen and were found to be severely impaired. However, the antigen-presenting capacity of both spleen cells and thioglycollate-induced peritoneal cells was found to be intact.
从出生日起,给小鼠注射兔抗小鼠IgM抗血清或纯化的兔抗小鼠IgM抗体。通过荧光激活细胞分选仪(FACS-II)上的特异性荧光抗体、多克隆B细胞有丝分裂原以及琼脂中的特异性沉淀分析,这些小鼠完全缺乏Ig阳性细胞或血清Ig。然后,用完全弗氏佐剂乳化的抗原对这些动物进行体内致敏,随后检测其引流淋巴结对相关抗原的体外T细胞增殖反应,发现其严重受损。然而,发现脾细胞和巯基乙酸盐诱导的腹腔细胞的抗原呈递能力是完整的。