Barbosa J E, Harrison R A, Barker P J, Lachmann P J
Faculdade de Medicina de Ribeirao-Preto-USP, Depto de Immunologia, Sao Paulo, Brazil.
Clin Exp Immunol. 1992 Jan;87(1):144-9. doi: 10.1111/j.1365-2249.1992.tb06428.x.
Previous studies of erythrocyte CR1 levels in systemic lupus erythematosus (SLE) and other diseases with in vivo complement activation have led to the conclusion that CR1 levels fall because of loss of CR1 from erythrocytes by proteolysis--predominantly in the liver. In order to measure the existence of proteolysed CR1 remnants on erythrocytes an antibody was raised to a peptide corresponding to the CR1 sequence between the proximal standard consensus repeat (SCR) and the transmembrane segment. This antipeptide antibody recognizes a neo-antigen found on trypsinized erythrocytes which has been demonstrated to represent the 'CR1-stump'. The anti-'CR1-stump' antiserum detects proteolysed CR1 on the ex vivo erythrocytes of a patient with cold haemolytic antibody disease (CHAD). However, higher affinity antibodies will be needed to make anti-CR1-stump a satisfactory diagnostic reagent.
以往对系统性红斑狼疮(SLE)及其他体内补体激活疾病患者红细胞CR1水平的研究得出结论,CR1水平下降是由于红细胞上的CR1经蛋白水解作用丧失,主要发生在肝脏。为了检测红细胞上经蛋白水解的CR1残余物的存在,制备了一种针对与近端标准共有重复序列(SCR)和跨膜区段之间的CR1序列对应的肽段的抗体。这种抗肽抗体识别胰蛋白酶处理过的红细胞上发现的一种新抗原,该抗原已被证明代表“CR1残端”。抗“CR1残端”抗血清可检测冷凝集素病(CHAD)患者离体红细胞上经蛋白水解的CR1。然而,需要更高亲和力的抗体才能使抗CR1残端成为一种令人满意的诊断试剂。