Hebert L A, Birmingham D J, Shen X P, Cosio F G
Department of Internal Medicine, Ohio State University, Columbus 43210-1228.
Clin Immunol Immunopathol. 1992 Mar;62(3):301-6. doi: 10.1016/0090-1229(92)90107-y.
Erythrocyte complement receptors (CR) are unique to primates and play a role in the clearance of immune complexes from the circulation. Immune complex-mediated diseases (e.g., systemic lupus erythematosus, SLE) cause decreased erythrocyte CR levels, resulting in decreased capacity of the erythrocytes to bind immune complexes that form in the circulation. Thus, raising erythrocyte CR levels might benefit patients with immune complex-mediated diseases. Because young erythrocytes express more CR than old erythrocytes, increasing erythropoiesis should increase the average number of CR expressed per erythrocyte. The present study was undertaken to test that hypothesis. Erythropoiesis was stimulated in nine cynomolgus monkeys (CYN) by weekly phlebotomy (30% of blood volume was removed, erythrocytes were discarded, and leukocytes were returned to the animal) for 8 weeks. Sham phlebotomy (30% of blood removed, then all components returned to the animal) was carried out weekly in four additional CYN for a period of 4 to 8 weeks. Sham phlebotomy did not change any of the parameters measured. However, phlebotomy resulted in a progressive increase in the mean number of CR expressed per erythrocyte (CR/erythrocyte): 2780 +/- 700 to 4230 +/- 820, P less than 0.0005. The increase in erythrocyte CR was first detected at about 2 weeks after the start of phlebotomy and was sustained through the course of phlebotomy. The increase in CR/erythrocyte included an increase in the percentage of erythrocyte expressing CR in clusters (37.9 +/- 6.4 vs 50.8 +/- 8.7%, P less than 0.01) as demonstrated by a flow cytometry study of the binding of fluorescent beads coated with anti-CR1 antibody. No significant change in leukocyte or platelet counts were observed. We conclude that stimulating erythropoiesis causes an increase in CR/erythrocyte. The magnitude of the increase suggests that it could be biologically significant.
红细胞补体受体(CR)是灵长类动物所特有的,在从循环中清除免疫复合物方面发挥作用。免疫复合物介导的疾病(如系统性红斑狼疮,SLE)会导致红细胞CR水平降低,从而使红细胞结合循环中形成的免疫复合物的能力下降。因此,提高红细胞CR水平可能对免疫复合物介导的疾病患者有益。由于年轻红细胞比衰老红细胞表达更多的CR,增加红细胞生成应会增加每个红细胞表达的CR平均数量。本研究旨在验证这一假设。对9只食蟹猴(CYN)进行每周一次的放血(去除30%血容量,丢弃红细胞,将白细胞回输动物体内)以刺激红细胞生成,持续8周。另外4只CYN每周进行假放血(去除30%血液,然后将所有成分回输动物体内),持续4至8周。假放血未改变所测量的任何参数。然而,放血导致每个红细胞表达的CR平均数量(CR/红细胞)逐渐增加:从2780±700增至4230±820,P<0.0005。红细胞CR的增加在放血开始约2周后首次检测到,并在放血过程中持续存在。通过对包被抗CR1抗体的荧光珠结合情况进行流式细胞术研究表明,CR/红细胞的增加包括成簇表达CR的红细胞百分比增加(37.9±6.4对50.8±8.7%,P<0.01)。未观察到白细胞或血小板计数有显著变化。我们得出结论,刺激红细胞生成会导致CR/红细胞增加。增加的幅度表明其可能具有生物学意义。