Maianskiĭ D N
Biull Eksp Biol Med. 1976 Aug;82(8):974-7.
Intraperitoneal transplantation of 0.5 x 10(7), 1 x 10(7) or 2 x 10(7) spleen cells from the C57BL mice to newborn CBA recipients induced an acute form or runt disease which resulted in the death of 43%, 86% or 95% of the recipient mice, respectively, in the course of 2--3 weeks after the cell transfer. Preliminary immunization of C57BL donors with CBA isoantigens led to a marked enhancement, and immunization with foreign antigens (sheep red blood cells)--to weakening the reaction. In reverse combination of mouse strains the runt disease was 4--5 times less severe and no "preimmunization effect" occurred. In C57BL leads to CBA combination the reaction was accompanied by proliferation of pyroninophilic mononuclears and follicular destruction, while in the CBA leads to C57BL combination-by the retardation of their growth.
将0.5×10⁷、1×10⁷或2×10⁷个C57BL小鼠的脾细胞腹腔内移植给新生CBA受体,会引发急性型矮小病,在细胞移植后的2至3周内,分别导致43%、86%或95%的受体小鼠死亡。用CBA同种抗原对C57BL供体进行预先免疫会导致反应显著增强,而用异种抗原(绵羊红细胞)免疫则会减弱反应。在小鼠品系的反向组合中,矮小病的严重程度降低4至5倍,且未出现“预先免疫效应”。在C57BL→CBA组合中,反应伴随着嗜派洛宁单核细胞的增殖和滤泡破坏,而在CBA→C57BL组合中,则伴随着它们生长的迟缓。