Muscari A, Puddu G M, Bozzoli C, Volta U, Sangiorgi Z, Bianchi F B, Descovich G C, Puddu P
Istituto di Patologia Speciale Medica e Metodologia Clinica, Università degli Studi di Bologna.
Ann Ital Med Int. 1992 Jan-Mar;7(1):7-12.
Total serum IgA and IgA antibodies to some milk antigens are often associated with severe atherosclerosis. In the present study we examined the same serum samples to evaluate the possible involvement of serum IgA antibodies to apoproteins and lipoproteins and their relationship to IgA antibodies to milk antigens. We studied 23 subjects with angiographically assessed atherosclerotic lesions (ATS group) and 20 healthy control subjects with a similar age range (59-69 years) and sex distribution. Anti-ApoB, Apo A-I, Apo A-II and anti-LDL, VLDL and HDL antibodies were measured with the ELISA method. All antibodies tested except those to anti-Apo A-I were significantly higher in the ATS group with respect to controls with a maximum significance for anti-Apo B IgA (p = 0.0018). When, for each antibody, a threshold of positivity was set to the mean + 2 SD of values in the control group, 12 ATS subjects (52%) and 1 control (5%) were found to be positive for either anti-Apo B or anti-Apo A-II IgA. Most of the correlations of anti-apoprotein and anti-lipoprotein IgA with anti-milk protein IgA and total IgA were significant. The association of these antibodies with atherosclerosis might either be specific or represent part of a polyclonal IgA response. Whether this association is a cause or an effect of atherosclerotic disease is presently unknown.
血清总IgA以及针对某些牛奶抗原的IgA抗体通常与严重动脉粥样硬化相关。在本研究中,我们检测了相同的血清样本,以评估血清中针对载脂蛋白和脂蛋白的IgA抗体的可能作用及其与针对牛奶抗原的IgA抗体的关系。我们研究了23例经血管造影评估有动脉粥样硬化病变的受试者(动脉粥样硬化组)和20例年龄范围相似(59 - 69岁)且性别分布相同的健康对照受试者。采用酶联免疫吸附测定法检测抗载脂蛋白B、载脂蛋白A - I、载脂蛋白A - II以及抗低密度脂蛋白、极低密度脂蛋白和高密度脂蛋白抗体。除抗载脂蛋白A - I抗体外,动脉粥样硬化组中所有检测的抗体相对于对照组均显著更高,其中抗载脂蛋白B IgA的差异具有最大显著性(p = 0.0018)。对于每种抗体,当将阳性阈值设定为对照组均值 + 2个标准差时,发现12例动脉粥样硬化组受试者(52%)和1例对照受试者(5%)的抗载脂蛋白B或抗载脂蛋白A - II IgA呈阳性。抗载脂蛋白和抗脂蛋白IgA与抗牛奶蛋白IgA及总IgA之间的大多数相关性均具有显著性。这些抗体与动脉粥样硬化的关联可能是特异性的,或者代表多克隆IgA反应的一部分。目前尚不清楚这种关联是动脉粥样硬化疾病的原因还是结果。