Müller Norbert, Schwarz Markus J
Department of Psychiatry and Psychotherapy Ludwig-Maximilians-Universität Munchen, Germany.
Curr Immunol Rev. 2010 Aug;6(3):213-220. doi: 10.2174/157339510791823673.
Although an immune dysfunction and the involvement of infectious agents in the pathophysiology of schizophrenia are discussed since decades, the field never came into the mainstream of research. In schizophrenia a blunted type-1 immune response seems to be associated with a dysbalance in the activation of the enzyme indoleamine 2,3-dioxygenase (IDO) and in the tryptophan - kynurenine metabolism resulting in increased production of kynurenic acid in schizophrenia. This is associated with an imbalance in the glutamatergic neurotransmission, leading to an NMDA antagonism in schizophrenia. The immunological effects of antipsychotics rebalance partly the immune imbalance and the overweight of the production of the kynurenic acid. This immunological imbalance results in an inflammatory state combined with increased prostaglandin E(2) (PGE(2)) production and increased cyclo-oxygenase-2 (COX-2) expression. COX-2 inhibitors have been tested in clinical trials, pointing to favourable effects in schizophrenia.
尽管数十年来人们一直在讨论免疫功能障碍以及感染因素在精神分裂症病理生理学中的作用,但该领域从未成为研究的主流。在精神分裂症中,迟钝的1型免疫反应似乎与吲哚胺2,3-双加氧酶(IDO)的激活失衡以及色氨酸 - 犬尿氨酸代谢失衡有关,导致精神分裂症中犬尿酸的产生增加。这与谷氨酸能神经传递失衡有关,导致精神分裂症中的NMDA拮抗作用。抗精神病药物的免疫作用部分地重新平衡了免疫失衡以及犬尿酸产生过多的情况。这种免疫失衡导致炎症状态,伴有前列腺素E2(PGE2)产生增加和环氧化酶-2(COX-2)表达增加。COX-2抑制剂已在临床试验中进行了测试,显示出对精神分裂症有有利影响。