Cooper K M, Moore M, Hilton A M
Clin Exp Immunol. 1981 Jul;45(1):18-28.
Sera from patients with chronic lung diseases were tested for the presence of immune complexes (ICs) by the 125I-C1q-binding assay. Contrary to earlier reports, modification of the test system by addition of heparin decreased rather than increased the ability of the test to discriminate between control and pathological sera. Using the unmodified system, elevated C1q-binding activity (C1qBA) was found in patients with asthma (18%), chronic bronchitis (18%), sarcoidosis (18%), fibrosing alveolitis (50%), bronchogenic carcinoma (52%) and bronchiectasis (67%). Studies with the reducing agent 2-mercaptoethanol (2-ME) suggested a role for IgM rheumatoid factor (RF) and/or IgG-containing complexes in the C1q-reactive material of sera from patients with bronchiectasis and bronchogenic carcinoma. In the latter two groups, C1qBA was found to correlate with serum levels of IgG and IgA but not with C3 and C4. A weak condition between levels of C-reactive protein (CRP) and C1qBA was found in the bronchogenic carcinoma group. Carcinoembryonic antigen (CEA) levels were elevated in all groups studied but no correlation with C1qBA was demonstrated, suggesting that CEA and CEA-ICs, if present, do not have an influence on the C1qBA of such sera. The results indicate that elevated serum C1qBA is a concomitant of both chronic inflammatory and neoplastic diseases of the lung but the extent of any similarity in the non-immunoglobulin components of the immune complexes in the respective conditions remains unknown.
采用¹²⁵I - C1q结合试验检测慢性肺部疾病患者血清中免疫复合物(ICs)的存在情况。与早期报告相反,通过添加肝素对检测系统进行改良后,检测系统区分对照血清和病理血清的能力降低而非提高。使用未改良的系统,发现哮喘患者(18%)、慢性支气管炎患者(18%)、结节病患者(18%)、肺纤维化患者(50%)、支气管源性癌患者(52%)和支气管扩张患者(67%)的C1q结合活性(C1qBA)升高。用还原剂2 - 巯基乙醇(2 - ME)进行的研究表明,IgM类风湿因子(RF)和/或含IgG的复合物在支气管扩张和支气管源性癌患者血清的C1q反应性物质中起作用。在后两组中,发现C1qBA与血清IgG和IgA水平相关,但与C3和C4无关。在支气管源性癌组中发现C反应蛋白(CRP)水平与C1qBA之间存在微弱关联。在所研究的所有组中癌胚抗原(CEA)水平均升高,但未显示与C1qBA相关,这表明CEA和CEA - ICs(如果存在)对此类血清的C1qBA没有影响。结果表明,血清C1qBA升高是肺部慢性炎症和肿瘤性疾病的共同特征,但在各自情况下免疫复合物的非免疫球蛋白成分的相似程度仍不清楚。