Portanova J P, Kotzin B L, Coleman E A, Claman H N
Cell Immunol. 1984 Sep;87(2):485-93. doi: 10.1016/0008-8749(84)90017-0.
Using a histone-specific plaque assay, we examined anti-histone-antibody (AHA) production at the organ level in the autoimmune NZB/NZW strain. The spleen had the highest absolute numbers of AHA-secreting cells. High percentages of immunoglobulin-secreting cells producing AHA were characteristic of spleen and bone marrow but not lymph node. AHA-secreting cells were detected in NZB/NZW mice with elevated serum activity but not in mice with normal serum levels. Serum AHA activity correlated with the number of AHA-secreting cells in the spleen but not with the total number of immunoglobulin-secreting cells in the spleen nor with the total serum immunoglobulin level. These findings concerning the organ distribution of AHA-secreting cells contrast with results of other investigators studying autoantibodies of other specificities. Furthermore, our results suggest that AHA production does not solely result from a generalized increase in total immunoglobulin synthesis present in NZB/NZW mice.
我们使用一种组蛋白特异性蚀斑试验,在自身免疫性NZB/NZW品系小鼠的器官水平检测抗组蛋白抗体(AHA)的产生。脾脏中分泌AHA的细胞绝对数量最高。分泌AHA的免疫球蛋白分泌细胞的高比例是脾脏和骨髓的特征,但淋巴结并非如此。在血清活性升高的NZB/NZW小鼠中检测到了分泌AHA的细胞,但在血清水平正常的小鼠中未检测到。血清AHA活性与脾脏中分泌AHA的细胞数量相关,但与脾脏中免疫球蛋白分泌细胞的总数以及血清总免疫球蛋白水平均无关。这些关于分泌AHA细胞的器官分布的发现与其他研究其他特异性自身抗体的研究者的结果形成对比。此外,我们的结果表明,AHA的产生并非仅仅源于NZB/NZW小鼠中总免疫球蛋白合成的普遍增加。