Lepez Trees, Vandewoestyne Mado, Deforce Dieter
Chimerism. 2013 Oct-Dec;4(4):111-8. doi: 10.4161/chim.25055. Epub 2013 May 20.
Autoimmune thyroid diseases (AITD) show a female predominance, with an increased incidence in the years following parturition. Fetal microchimerism has been suggested to play a role in the pathogenesis of AITD. However, only the presence of fetal microchimeric cells in blood and in the thyroid gland of these patients has been proven, but not an actual active role in AITD. Is fetal microchimerism harmful for the thyroid gland by initiating a Graft versus Host reaction (GvHR) or being the target of a Host versus Graft reaction (HvGR)? Is fetal microchimerism beneficial for the thyroid gland by being a part of tissue repair or are fetal cells just innocent bystanders in the process of autoimmunity? This review explores every hypothesis concerning the role of fetal microchimerism in AITD.
自身免疫性甲状腺疾病(AITD)表现出女性优势,在分娩后的几年中发病率增加。胎儿微嵌合体被认为在AITD的发病机制中起作用。然而,仅证实了这些患者血液和甲状腺中存在胎儿微嵌合细胞,但并未证实其在AITD中实际发挥的积极作用。胎儿微嵌合体是通过引发移植物抗宿主反应(GvHR)对甲状腺有害,还是成为宿主抗移植物反应(HvGR)的靶标?胎儿微嵌合体作为组织修复的一部分对甲状腺有益,还是胎儿细胞在自身免疫过程中只是无辜的旁观者?本综述探讨了关于胎儿微嵌合体在AITD中作用的各种假设。