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首页> 外文期刊>Developmental Immunology: Journal of Immunology Research >Antigenic Complementarity in the Origins of Autoimmunity: A General Theory Illustrated With a Case Study of Idiopathic Thrombocytopenia Purpura
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Antigenic Complementarity in the Origins of Autoimmunity: A General Theory Illustrated With a Case Study of Idiopathic Thrombocytopenia Purpura

机译:自身免疫起源中的抗原互补性:以特发性血小板减少性紫癜为例的一般理论说明

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We describe a novel, testable theory of autoimmunity, outline novel predictions made by the theory, and illustrate its application to unravelling the possible causes of idiopathic thrombocytopenia purpura (ITP). Pairs of stereochemically complementary antigens induce complementary immune responses (antibody or T-cell) that create loss of regulation and civil war within the immune system itself. Antibodies attack antibodies creating circulating immune complexes; T-cells attack T-cells creating perivascular cuffing. This immunological civil war abrogates the self-nonself distinction. If at least one of the complementary antigens mimics a self antigen, then this unregulated immune response will target host tissues as well. Data demonstrating that complementary antigens are found in some animal models of autoimmunity and may be present in various human diseases, especially ITP, are reviewed. Specific mechanisms for preventing autoimmunity or suppressing existing autoimmunity are derived from the theory, and critical tests proposed. Finally, we argue that Koch's postulates are inadequate for establishing disease causation for multiple-antigen diseases and discuss the possibility that current research has failed to elucidate the causes of human autoimmune diseases because we are using the wrong criteria.
机译:我们描述了一种新颖的,可测试的自身免疫理论,概述了该理论做出的新颖预测,并阐明了其在阐明特发性血小板减少性紫癜(ITP)可能原因方面的应用。成对的立体化学互补抗原诱导互补的免疫反应(抗体或T细胞),从而在免疫系统自身内部造成调节失调和内战。抗体攻击抗体,形成循环免疫复合物。 T细胞攻击T细胞,形成血管周围的套囊。这场免疫内战废除了自我-非自我的区分。如果至少一种互补抗原模拟自身抗原,那么这种不受调节的免疫反应也将靶向宿主组织。审查了证明互补抗原在某些自身免疫性动物模型中发现并可能存在于各种人类疾病(尤其是ITP)中的数据。从理论中得出了预防自身免疫或抑制现有自身免疫的特定机制,并提出了关键试验。最后,我们认为科赫的假设不足以建立多种抗原疾病的病因,并讨论了由于我们使用的标准错误而导致当前研究未能阐明人类自身免疫性疾病的原因的可能性。

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