Jung L K, Good R A, Fernandes G
J Immunol. 1984 Mar;132(3):1265-70.
Autoimmune-prone (NZB X NZW)F1 (B/W) mice have been shown to have a variety of immunologic perturbations. However, most studies have been performed with spleen cells. By using the Mishell-Dutton culture system, we examined the in vitro immune response of the various lymphoid tissue to determine whether an imbalance at a selective lymphoid site may exist in B/W mice. It was shown that the ability of mesenteric lymph node (MLN) cells of B/W mice to generate plaque-forming cells (PFC) in response to sheep red blood cells was consistently less than that of the spleen cells. This relationship held true in the aged mice. In contrast, the ability of the MLN cells of other strains not prone to develop autoimmunity to generate PFC was higher than that of the spleen cells. No significant difference in the mitogenic response of the lymphoid cells from various lymphoid tissue in the young B/W mice was seen, as compared with normal lymphoid cells from control mice. However, it was demonstrated that a relative decrease of B cells and immunoregulatory Lyt-123+ cells in the MLN in the B/W mice occurred early in life, and it was concluded that this abnormality may account for the low PFC response observed.
自身免疫易感(NZB×NZW)F1(B/W)小鼠已被证明存在多种免疫紊乱。然而,大多数研究是用脾细胞进行的。通过使用米舍尔-达顿培养系统,我们检测了各种淋巴组织的体外免疫反应,以确定B/W小鼠的选择性淋巴部位是否可能存在失衡。结果显示,B/W小鼠肠系膜淋巴结(MLN)细胞对绵羊红细胞产生空斑形成细胞(PFC)的能力始终低于脾细胞。这种关系在老年小鼠中也成立。相比之下,其他不易发生自身免疫的品系的MLN细胞产生PFC的能力高于脾细胞。与对照小鼠的正常淋巴细胞相比,年轻B/W小鼠各种淋巴组织的淋巴细胞有丝分裂反应没有显著差异。然而,已证明B/W小鼠MLN中B细胞和免疫调节性Lyt-123+细胞在生命早期就出现相对减少,得出的结论是,这种异常可能是观察到的低PFC反应的原因。