Lilliehöök B, Blomgren H
Department of Tumour Biology, Karolinska Institute, Stockholm, Sweden.
Scand J Immunol. 1980;11(2):181-6. doi: 10.1111/j.1365-3083.1980.tb00225.x.
Lymphocytes from C3H x CBA hybrid mice proliferate intensely in the spleens of irradiated CBA mice. Pretreatment of the CBA hosts with C3H x CBA spleen cells, known to specifically reduce the T-cell reactivity of the hosts against the strongly stimulatory Mls-antigen determined by the C3H-genome, abolished the capacity of the host to promote proliferation of C3H x CBA lymphocytes. In contrast, proliferation of C3H x CBA bone marrow cells, as measured by splenic 59Fe incorporation, was unaffected by such pretreatment. By examining the capacity of spleen cell populations of (C3H x CBA) x CBA back-cross mice to inhibit lymphocyte proliferation, as described above, and to express the C3H-determined Mls-antigen, it was concluded that these two traits are associated.
来自C3H×CBA杂交小鼠的淋巴细胞在受照射的CBA小鼠脾脏中强烈增殖。用C3H×CBA脾细胞对CBA宿主进行预处理,已知该脾细胞能特异性降低宿主针对由C3H基因组决定的强刺激性Mls抗原的T细胞反应性,从而消除了宿主促进C3H×CBA淋巴细胞增殖的能力。相比之下,通过脾内59Fe掺入法测定,C3H×CBA骨髓细胞的增殖不受这种预处理的影响。通过检查(C3H×CBA)×CBA回交小鼠脾细胞群体抑制淋巴细胞增殖的能力(如上所述)以及表达由C3H决定的Mls抗原的能力,得出这两个特性是相关联的结论。