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Murine models for studying treatment, prevention and pathogenesis of FNAIT

机译:用于学习治疗,预防和Fnait发病机制的小鼠模型

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摘要

Maternal alloimmunization to paternally inherited antigens on fetal/neonatal platelets can cause fetal/neonatal alloimmune thrombocytopenia (FNAIT) after antibody-mediated removal of platelets from the fetal circulation. The complications vary from mild bleeding symptoms to severe intracranial hemorrhage and subsequent neurological impairment or death. Studies on in vivo mechanisms are challenging to measure directly in pregnant women, rendering murine models as valuable and attractive alternatives, despite some critical differences between mice and men affecting the translational value. Here we present and discuss, the different murine models that substantially have increased our knowledge and understanding of FNAIT pathogenesis - as well as preclinical evaluation of therapeutic and preventive strategies.
机译:母体同种异体在胎儿/新生儿血小板上对患者遗传抗原可引起抗体介导的胎儿血液移除血液循环后胎儿/新生儿同种疫血小板减少症(FNAIT)。 并发症因轻度出血症状而变化,以严重颅内出血和随后的神经系统损伤或死亡。 在体内机制中的研究挑战直接在孕妇中衡量,尽管小鼠与男性之间的临界差异,但是呈现有价值和有吸引力的替代品,尽管小鼠与男性影响了翻译价值。 在这里,我们展示并讨论了不同的鼠模型,这些小鼠模型显着提高了对Fnait发病机制的知识和理解 - 以及治疗和预防策略的临床前评估。

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