Yahya M D, Pinnas J L, Meinke G C, Lung C C
Department of Microbiology, Faculty of Life Sciences, University Kebangsaan, Malaysia.
J Autoimmun. 1996 Feb;9(1):3-9. doi: 10.1006/jaut.1996.0002.
Previous studies have shown that lipid peroxidative processes may play a role in disease pathogenesis in lupus-prone MRL/lpr mice. Studies were thus performed to determine if an immune response against malondialdehyde (MDA), a highly reactive byproduct of lipid peroxidation, was present in these mice. By using MDA-modified mouse serum albumin (MSA) as antigens in ELISA, we found that these mice produce high levels of MDA-specific antibodies in the complement-fixing IgG2a and IgG2b subclasses. Anti-MDA antibodies were also found in MRL/+ mice but in significantly lower levels. The specificity of these antibodies was verified by inhibition ELISA. MDA may contribute to disease pathogenesis in these mice by altering the immunogenicity of self molecules, eliciting an immune response and forming immune complexes that may deposit in tissues.
先前的研究表明,脂质过氧化过程可能在易患狼疮的MRL/lpr小鼠的疾病发病机制中起作用。因此进行了研究,以确定这些小鼠是否存在针对丙二醛(MDA)的免疫反应,丙二醛是脂质过氧化的一种高反应性副产物。通过在ELISA中使用MDA修饰的小鼠血清白蛋白(MSA)作为抗原,我们发现这些小鼠在补体固定IgG2a和IgG2b亚类中产生高水平的MDA特异性抗体。在MRL/+小鼠中也发现了抗MDA抗体,但水平明显较低。这些抗体的特异性通过抑制ELISA得到验证。MDA可能通过改变自身分子的免疫原性、引发免疫反应以及形成可能沉积在组织中的免疫复合物,从而在这些小鼠的疾病发病机制中发挥作用。