Berrens L, de la Faille H B, Borst-Eilers E
J Clin Pathol. 1979 Jun;32(6):528-33. doi: 10.1136/jcp.32.6.528.
A patient with systemic lupus erythematosus was studied whose blood serum on repeated occasions showed undetectable levels of haemolytic omplement (C). A detailed investigation of individual C components in the serum of the proposita and her family revealed the absence of functional C2 in the patient and half-normal values in the relatives. C4 levels in the family, but not in the patient, were above normal, whereas the levels of factor B were low in all cases. No abnormalities were noted in C3, C9, or C1INH. Tissue typing showed linkage of the C2-deficiency gene with the HLA-A10/B18 and A9/B18 haplotypes. No linkage with red cell antigens and no relationship with plasma kallikrein levels was found.
对一名系统性红斑狼疮患者进行了研究,其血清多次检测显示溶血补体(C)水平无法检测到。对先证者及其家族血清中的各个补体成分进行详细调查发现,患者体内缺乏功能性C2,其亲属体内C2水平为正常值的一半。家族中C4水平(患者除外)高于正常,而所有病例中B因子水平均较低。C3、C9或C1INH未发现异常。组织分型显示C2缺陷基因与HLA-A10/B18和A9/B18单倍型连锁。未发现与红细胞抗原连锁,也未发现与血浆激肽释放酶水平有关。