Ríhová B, Vĕtvicka V, Ríha I, Holán V
Thymus. 1986;8(3):161-9.
The SRBC-pulsed peritoneal macrophages from low IgG producing B10 mice were defective in induction of primary as well as secondary antibody responses in (A/J X B10)F1 recipients. This is most probably due to a low number of Ia+ macrophages in the defective B10 mice. Immunization caused a significant increase in numbers of Lyt 2+ cells in spleens of the B10 strain, whereas the percentage of L3T4+ cells remained unchanged. The opposite situation was found in mice of the high responding A/J strain. Simultaneous application of LPS and SRBC prevented the elevated appearance of Lyt 2+ cells in spleens of low responding B10 mice.
来自低IgG产生的B10小鼠的经绵羊红细胞(SRBC)脉冲处理的腹腔巨噬细胞,在诱导(A/J×B10)F1受体小鼠的初次及二次抗体反应方面存在缺陷。这很可能是由于缺陷型B10小鼠中Ia⁺巨噬细胞数量较少。免疫导致B10品系小鼠脾脏中Lyt 2⁺细胞数量显著增加,而L3T4⁺细胞的百分比保持不变。在高反应性的A/J品系小鼠中发现了相反的情况。同时应用脂多糖(LPS)和SRBC可防止低反应性B10小鼠脾脏中Lyt 2⁺细胞数量的增加。