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Interleukin-12 inhibits development of ectopic endometriotic tissues in peritoneal cavity via activation of NK cells in a murine endometriosis model

机译:白细胞介素12通过激活小鼠子宫内膜异位症模型中的NK细胞抑制腹膜腔内异位子宫内膜异位组织的发育

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摘要

Involvement of impaired peritoneal immunosurveillance systems has been well established in the pathology of endometriosis. On the other hand, it has been observed that peritoneal administration of IL-12 suppress development of endometriotic lesions in a mouse endometriosis model. We investigated the effect of peritoneal administration of IL-12 on the peritoneal immunosurveillance system regarding NK cells in the mouse model. Treating the endometrial-tissue challenged mice with IL-12 for 5 consecutive days, from day -2 to day 2 (implantation of the endometrial tissues was done on day 0), cytotoxicity of splenic NK cells was enhanced immediately after the administration, on day 3, and development of the endometriotic lesions was reduced on day 21. In vivo NK cell depletion by administration of anti-IL-2Rβ mAb resulted in reduction of the cytotoxicity of splenic NK cells concomitant with a significant attenuation of suppressive effect of IL-12 on development of endometriotic lesions. Therefore, it was suggested that IL-12 suppresses development of endometriotic lesions via activation of NK cells, and that NK cells are involved in the primary defense for the development of endometriotic lesions.
机译:在子宫内膜异位症的病理学中已经充分证实了受损的腹膜免疫监视系统的参与。另一方面,已经观察到腹膜给予IL-12在小鼠子宫内膜异位症模型中抑制了子宫内膜异位病变的发展。我们调查了腹腔注射IL-12对小鼠模型中有关NK细胞的腹膜免疫监视系统的影响。从第-2天到第2天连续5天用IL-12处理经子宫内膜组织攻击的小鼠(在第0天完成子宫内膜组织的植入),在给药后第2天立即增强脾NK细胞的细胞毒性。如图3所示,子宫内膜异位病变的发展在第21天减少。通过施用抗IL-2RβmAb的体内NK细胞耗竭导致脾脏NK细胞的细胞毒性降低,同时IL-12的抑制作用显着减弱。对子宫内膜异位病变的发展。因此,提示IL-12通过激活NK细胞来抑制子宫内膜异位病变的发展,并且NK细胞参与了子宫内膜异位病变发展的主要防御作用。

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