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Physiology and endocrinology symposium: maternal immunological adjustments to pregnancy and parturition in ruminants and possible implications for postpartum uterine health: is there a prepartum-postpartum nexus?

机译:生理学和内分泌学研讨会:孕妇对反刍动物妊娠和分娩的免疫学调节及其对产后子宫健康的可能影响:是否存在产前产后关系?

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Establishment of microbial infections in the reproductive tract can have negative consequences for reproductive function of the postpartum female. Most periparturient cows experience bacterial contamination of the uterus after parturition, but only a fraction of these develop subclinical or clinical disease. It is not well understood why one female resolves uterine infections after parturition while another develops disease. Perhaps those that develop metritis or endometritis are exposed to a greater bacterial load at parturition than those that successfully restore the uterus to a healthy condition. A second possibility is that females that develop bacterial disease have compromised immune function, either systemically or in the reproductive tract and associated lymph nodes. Here, the possibility is raised that maternal immunological adjustments to the presence of the allogeneic conceptus may predispose some females to metritis or endometritis. Several regulatory processes ensure that adaptive immune responses against paternal antigens on the conceptus are downregulated during pregnancy. Among these are immunosuppressive effects of progesterone, local accumulation of immune cells that can inhibit inflammation and T cell responses, including M2 macrophages and gamma delta T cells, and differentiation of regulatory T cells to inhibit alloreactive lymphocytes. Some immunological adjustments to the conceptus also make the uterus more susceptible to bacterial infection. For example, progesterone not only depresses skin graft rejection but also reduces uterine capacity to eliminate bacterial infections. Macrophages of M2 phenotype can inhibit inflammation and facilitate persistence of some microbial infections. At parturition, immune defenses in the uterus may be further weakened by loss of the luminal epithelium of the endometrium, which is part of the innate immune system, as well as by disappearance of intraepithelial gamma delta T cells that produce the antibacterial proteins granulysin and perforin. It is currently not known whether molecules and cells that inhibit immune responses during pregnancy persist after parturition but, if so, they could contribute to compromised immune function in the uterus. It is hypothesized that individual variation in immune adjustments to pregnancy and parturition and the reversal of these changes in the postpartum period are important determinants of susceptibility of the uterus to infection.
机译:在生殖道中建立微生物感染会对产后女性的生殖功能产生负面影响。大多数围产期母牛在分娩后会受到子宫细菌的污染,但是其中只有一小部分会发展为亚临床或临床疾病。为何一位女性在分娩后解决子宫感染而另一位女性发展出疾病却为何仍未完全了解。与那些成功使子宫恢复健康状态的人相比,那些可能发展为子宫炎或子宫内膜炎的人在分娩时会承受更大的细菌负荷。第二种可能性是,患有细菌性疾病的女性全身或在生殖道以及相关的淋巴结中都削弱了免疫功能。在这里,存在这样的可能性,即母体对同种异体概念存在的免疫学调节可能会使某些女性易患子宫炎或子宫内膜炎。几个调节过程可确保在怀孕期间针对概念上针对父体抗原的适应性免疫反应被下调。其中包括孕酮的免疫抑制作用,可以抑制炎症和T细胞反应的免疫细胞的局部蓄积,包括M2巨噬细胞和伽马三角洲T细胞,以及调节性T细胞的分化以抑制同种反应性淋巴细胞。对概念的一些免疫学调整也使子宫更容易受到细菌感染。例如,孕酮不仅抑制皮肤移植排斥,而且降低子宫消除细菌感染的能力。 M2表型的巨噬细胞可以抑制炎症并促进某些微生物感染的持续存在。分娩时,子宫内膜腔上皮的丧失可能会进一步削弱子宫的免疫防御能力,子宫内膜是先天免疫系统的一部分,上皮内γ-δT细胞的消失会产生抗菌蛋白颗粒溶素和穿孔素。目前尚不知道在分娩后能抑制妊娠期间免疫反应的分子和细胞是否会持续存在,但如果这样,它们可能会导致子宫的免疫功能受损。据推测,针对妊娠和分娩的免疫调节的个体差异以及产后时期这些变化的逆转是子宫对感染易感性的重要决定因素。

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