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氧自由基使人类免疫球蛋白G变性,并增加其与类风湿因子抗体的反应性。

Oxygen free radicals denature human IgG and increase its reactivity with rheumatoid factor antibody.

作者信息

Lunec J, Griffiths H R, Brailsford S

机构信息

Department of Biochemistry, Selly Oak Hospital, Birmingham, United Kingdom.

出版信息

Scand J Rheumatol Suppl. 1988;75:140-7. doi: 10.3109/03009748809096755.

Abstract

Rheumatoid inflammation is characterised by the production of rheumatoid factor antibodies directed against denatured IgG. Oxygen free radicals have the potential to denature all manner of proteins and can be generated by activated phagocytic cells in the inflamed joint. By modifying routine ELISA and nephelometric procedures for measuring rheumatoid factor, (i.e. substituting free radical altered IgG for rabbit and heat aggregated IgG as antigens) we have observed that oxygen radicals, generated by (1) UV light and (2) PMA-activated neutrophils, give rise to monomeric and polymeric forms of IgG which have increased reactivity towards IgM and IgA polyclonal rheumatoid factor antibodies. We conclude that free radical alteration of IgG may be a stimulus to the formation of immune complexes with rheumatoid factor antibody, thereby promoting and amplifying tissue damage during rheumatoid inflammation.

摘要

类风湿性炎症的特征是产生针对变性IgG的类风湿因子抗体。氧自由基有可能使各种蛋白质变性,并且可由炎症关节中活化的吞噬细胞产生。通过改进用于测量类风湿因子的常规ELISA和比浊法程序(即用自由基改变的IgG替代兔和热聚集IgG作为抗原),我们观察到由(1)紫外线和(2)PMA激活的中性粒细胞产生的氧自由基会导致IgG的单体和聚合物形式,这些形式对IgM和IgA多克隆类风湿因子抗体的反应性增加。我们得出结论,IgG的自由基改变可能是刺激与类风湿因子抗体形成免疫复合物的因素,从而在类风湿性炎症期间促进和放大组织损伤。

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