Lapaire Olav, Hösli Irène, Zanetti-Daellenbach Rosanna, Huang Dorothy, Jaeggi Carmen, Gatfield-Mergenthaler Susanne, Hahn Sinuhe, Holzgreve Wolfgang
Department of Obstetrics and Gynecology, University of Basel, Switzerland.
J Matern Fetal Neonatal Med. 2007 Jan;20(1):1-5. doi: 10.1080/14767050601144834.
Microchimerism is defined by the presence of circulating cells, bi-directionally transferred from one genetically distinct individual to another. It occurs either physiologically during pregnancy, or iatrogenically after blood transfusion and organ transplants. The migrated cells may persist for decades. Much controversy exists around the role of microchimeric cells in the pathogenesis of various diseases and around their role in tissue repair. Microchimerism has been investigated in different autoimmune disorders, such as systemic sclerosis, systemic lupus erythematosus, autoimmune thyroid diseases, primary biliary cirrhosis and juvenile inflammatory myopathies. Recent data have demonstrated the promising role of microchimeric cells in the maternal response to tissue injuries by differentiating into many lineages. Therefore, further understanding of fetal-maternal microchimerism may help in anticipating its implications in disease as well as in more general women's health issues.
微嵌合体的定义是存在从一个基因不同的个体双向转移到另一个个体的循环细胞。它要么在孕期生理情况下出现,要么在输血和器官移植后医源性出现。迁移的细胞可能会持续数十年。关于微嵌合细胞在各种疾病发病机制中的作用以及它们在组织修复中的作用存在很多争议。人们已经在不同的自身免疫性疾病中研究了微嵌合体,如系统性硬化症、系统性红斑狼疮、自身免疫性甲状腺疾病、原发性胆汁性肝硬化和青少年炎性肌病。最近的数据表明,微嵌合细胞通过分化为多种谱系,在母体对组织损伤的反应中发挥着有前景的作用。因此,进一步了解胎儿 - 母体微嵌合体可能有助于预测其在疾病以及更广泛的女性健康问题中的影响。