Benaroch P, Bordenave G
Proc Natl Acad Sci U S A. 1984 May;81(9):2859-63. doi: 10.1073/pnas.81.9.2859.
Adult rabbits were sensitized against rabbit immunoglobulin allotypic specificities of the a and b series by means of two injections of their own lymphocytes coated with the appropriate IgG. The splenic lymphocytes from these sensitized rabbits were injected, 24 hr after birth, into newborns that had inherited from their father the allotypic specificities susceptible to recognition by the sensitized lymphocytes. A significant percentage (40%) of the young rabbits subjected to this treatment developed a total suppression of expression of these specificities with the well-known compensatory effect due to an increased expression of the corresponding allele. We have observed that the T Julius subset of the sensitized splenic lymphocytes was responsible for the induction of this suppression that was established without discernible intervention of anti-allotype antibodies. In one instance we observed that the expression of the allotypic specificities transmitted by the father, although established at 5 weeks of age, gradually declined and totally disappeared at 13 weeks of age.
成年兔通过两次注射自身涂有相应IgG的淋巴细胞,使其对a和b系列兔免疫球蛋白同种异型特异性产生致敏。在这些致敏兔出生24小时后,将其脾淋巴细胞注射到从父亲那里继承了易被致敏淋巴细胞识别的同种异型特异性的新生兔体内。接受这种处理的幼兔中有相当比例(40%)出现了这些特异性表达的完全抑制,并伴随着由于相应等位基因表达增加而产生的众所周知的补偿效应。我们观察到,致敏脾淋巴细胞的T Julius亚群负责诱导这种抑制,且这种抑制的建立没有抗同种异型抗体的明显干预。在一个实例中,我们观察到由父亲传递的同种异型特异性的表达,尽管在5周龄时就已确立,但在13周龄时逐渐下降并完全消失。