Sipos A, Czirják L, Lörincz G, Szegedi G
Third Department of Medicine, University Medical School of Debrecen, Hungary.
Scand J Rheumatol. 1988;17(1):43-50. doi: 10.3109/03009748809098758.
Autoantibodies may play a part in the pathogenesis of progressive systemic sclerosis (PSS). Anti-granulocyte antibodies have already been demonstrated in the sera of patients with PSS. In our study, anti-granulocyte antibodies were investigated by ELISA (enzyme linked immunosorbent assay) and cytotoxic tests. These antibodies were found in 18.4% of 38 patients. All the positive sera showed cold- and/or warm-reacting granulocytotoxic activity. No connection with granulocytopenia was found. The effect of patients' sera on normal granulocyte functions was also studied. Chemotaxis and binding of EA cells were inhibited independently of the presence of anti-granulocyte antibodies. Yeast phagocytosis and opsonized yeast phagocytosis were definitely reduced by sera containing anti-granulocyte antibodies. Anti-platelet autoantibodies were detected in 23.9% of the patients' sera, but no thrombocytopenia was found.
自身抗体可能在进行性系统性硬化症(PSS)的发病机制中起作用。抗粒细胞抗体已在PSS患者血清中得到证实。在我们的研究中,通过酶联免疫吸附测定(ELISA)和细胞毒性试验对抗粒细胞抗体进行了研究。在38例患者中有18.4%检测到这些抗体。所有阳性血清均显示出冷反应和/或温反应粒细胞毒性活性。未发现与粒细胞减少有关。还研究了患者血清对正常粒细胞功能的影响。趋化性和EA细胞的结合受到抑制,这与抗粒细胞抗体的存在无关。含抗粒细胞抗体的血清明显降低了酵母吞噬作用和调理酵母吞噬作用。在23.9%的患者血清中检测到抗血小板自身抗体,但未发现血小板减少症。