J Immunol:IL-11在多发性硬化症和自身免疫性脑脊髓炎中诱导脑炎性Th17细胞

2019-07-27 海北 MedSci原创

已有的研究显示,IL-11 + CD4 +细胞在患有早期复发 - 缓解型多发性硬化(MS)和活动性脑MS病变的患者的脑脊液中积聚。

已有的研究显示,IL-11 + CD4 +细胞在患有早期复发 - 缓解型多发性硬化(MS)和活动性脑MS病变的患者的脑脊液中积聚。

小鼠研究证实了IL-11在复发 - 缓解实验性自身免疫性脑脊髓炎(RREAE)恶化中的因果作用。

RREAE临床发作时施用IL-11可以诱导急性恶化,并增加临床评分,其在整个疾病过程中持续存在。IL-11增加了脊髓炎症灶的数量,以及外周和CNS浸润的IL-17 + CD4 +细胞数量,和IL-17A的血清水平。 

Ag召回分析显示,IL-11诱导IL-17A +GM-CSF +IL-21 + CD4 +髓鞘Ag反应性细胞。这些致脑炎CD4 + T细胞的被动转移诱导了严重的RREAE,其中IL-17A + CCR6 + CD4 +B细胞在CNS内积累。

此外,在单次剂量的IL-11后,来自具有RREAE的小鼠的非操作的CNS衍生的单核细胞的被动转移诱导了严重的RREAE,并且CNS内的IL-17A +CCR6 + CD4 +细胞的积累增加。

这些结果表明,IL-11可能作为早期自身免疫反应的生物标志物,也是早期复发缓解型MS患者的选择性治疗靶点。


原始出处:

Zhang X et al. IL-11 Induces Encephalitogenic Th17 Cells in Multiple Sclerosis and Experimental Autoimmune EncephalomyelitisJ Immunol, 2019; DOI: 10.4049/jimmunol.1900311.


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    2020-03-13 jml2009
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createdAvatar=, createdBy=4c37265, createdName=zhaojie88, createdTime=Mon Jul 29 05:36:00 CST 2019, time=2019-07-29, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1508243, encodeId=d3a715082431e, content=<a href='/topic/show?id=8d4596248e' target=_blank style='color:#2F92EE;'>#IL-1#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=39, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=9624, encryptionId=8d4596248e, topicName=IL-1)], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=f6cf9946833, createdName=jjjiang0202, createdTime=Mon Jul 29 05:36:00 CST 2019, time=2019-07-29, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=370408, encodeId=67f93e040898, content=学习了谢谢分享, beContent=null, objectType=article, channel=null, level=null, likeNumber=109, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=http://cacheapi.medsci.cn/resource/upload/20160304/IMG56D94856B1B5D6405.jpg, createdBy=27931687771, createdName=一个字-牛, createdTime=Sun Jul 28 15:57:49 CST 2019, time=2019-07-28, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=370356, encodeId=99353e035635, content=向科研人员致敬!, beContent=null, objectType=article, channel=null, level=null, likeNumber=93, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=, createdBy=e5171668917, createdName=坚强007, createdTime=Sat Jul 27 16:17:02 CST 2019, time=2019-07-27, status=1, ipAttribution=)]
    2020-03-10 xlysu
  5. 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  6. 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  7. 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createdAvatar=http://cacheapi.medsci.cn/resource/upload/20160304/IMG56D94856B1B5D6405.jpg, createdBy=27931687771, createdName=一个字-牛, createdTime=Sun Jul 28 15:57:49 CST 2019, time=2019-07-28, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=370356, encodeId=99353e035635, content=向科研人员致敬!, beContent=null, objectType=article, channel=null, level=null, likeNumber=93, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=, createdBy=e5171668917, createdName=坚强007, createdTime=Sat Jul 27 16:17:02 CST 2019, time=2019-07-27, status=1, ipAttribution=)]
    2019-07-29 zhaojie88
  8. 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createdAvatar=http://cacheapi.medsci.cn/resource/upload/20160304/IMG56D94856B1B5D6405.jpg, createdBy=27931687771, createdName=一个字-牛, createdTime=Sun Jul 28 15:57:49 CST 2019, time=2019-07-28, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=370356, encodeId=99353e035635, content=向科研人员致敬!, beContent=null, objectType=article, channel=null, level=null, likeNumber=93, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=, createdBy=e5171668917, createdName=坚强007, createdTime=Sat Jul 27 16:17:02 CST 2019, time=2019-07-27, status=1, ipAttribution=)]
    2019-07-29 jjjiang0202
  9. 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createdAvatar=http://cacheapi.medsci.cn/resource/upload/20160304/IMG56D94856B1B5D6405.jpg, createdBy=27931687771, createdName=一个字-牛, createdTime=Sun Jul 28 15:57:49 CST 2019, time=2019-07-28, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=370356, encodeId=99353e035635, content=向科研人员致敬!, beContent=null, objectType=article, channel=null, level=null, likeNumber=93, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=, createdBy=e5171668917, createdName=坚强007, createdTime=Sat Jul 27 16:17:02 CST 2019, time=2019-07-27, status=1, ipAttribution=)]
    2019-07-28 一个字-牛

    学习了谢谢分享

    0

  10. 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    2019-07-27 坚强007

    向科研人员致敬!

    0

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多发性硬化(MS)是一种对神经细胞造成渐进性损害的疾病,病灶中常有髓鞘脱失、炎症和胶质反应,在过去几十年里发病率不断上升。而大脑或脊髓中的病毒感染被认为是这种疾病的诱因。一些科学家认为,我们饮食方式的改变、卫生设施的改善或抗生素使用的增加导致生活在人体内部有益细菌的有害变化,潜在地增加MS和其他相关疾病的风险。

NEJM:口服BTK抑制剂治疗多发性硬化

研究认为,复发性多发性硬化症患者每日服用一次75毫克Evobrutinib,可显著减少钆增强病变明数目,但不同疗法年化复发率或残疾进展均无显著性差异