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受体对实验性变应性脑脊髓炎系列被动转移的贡献。

Recipient contributions to serial passive transfer of experimental allergic encephalomyelitis.

作者信息

Wegmann K W, Hinrichs D J

出版信息

J Immunol. 1984 May;132(5):2417-23.

PMID:6201543
Abstract

EAE can be adoptively transferred into normal recipients by the transfer of BP-specific EAE effector cells. After cell transfer, a series of ill-defined events occur in the recipient that culminate in the development of paralysis associated with neural tissue damage. We investigated the subsequent recipient response to the adoptively transferred disease and examined the role that recipient lymphocytes play in the development of adoptively transferred EAE. Recipient involvement was assessed by the transfer of EAE through a series of normal F1 animals as recipients and at the endpoint of the experiment, determining the MHC restriction pattern of the BP-sensitive cells present. The serial transfer of EAE from BP-CFA-sensitized LEW----(LEW X F-344)F1----(LEW X P2)F1, and from BP-CFA sensitized LEW----(LEW X F344)F1----(LEW X F-344)F1, resulted in the development of BP-sensitive cells in the spleens of the secondary recipients that were able to transfer disease into normal LEW recipients. To test directly for the development of host-derived BP-sensitive cells that might arise in the F1 animal, the serial transfer of EAE from LEW----(LEW X ACI)F1----(LEW X ACI)F1 was performed. When BP-sensitive cells obtained from the secondary (LEW X ACI)F1 recipient animal were transferred into either normal LEW and ACI, or irradiated LEW and ACI animals as final recipients, transfer of disease was successful only into the LEW parental. These results suggest that the development of passive EAE is due solely to the transferred BP-sensitive cells originating from the actively immunized donor, and that no host-derived lymphocytes are recruited into the pool of EAE effector precursor cells found in the spleen of animals after the development of adoptively transferred EAE.

摘要

实验性自身免疫性脑脊髓炎(EAE)可通过转移针对髓鞘碱性蛋白(BP)的EAE效应细胞而被动转移至正常受体。细胞转移后,受体中会发生一系列尚不明确的事件,最终导致与神经组织损伤相关的麻痹症状出现。我们研究了受体对被动转移疾病的后续反应,并考察了受体淋巴细胞在被动转移EAE发病过程中所起的作用。通过将EAE依次转移至一系列正常F1动物作为受体,并在实验终点确定所存在的对BP敏感细胞的主要组织相容性复合体(MHC)限制模式,来评估受体的参与情况。将EAE从用BP-完全弗氏佐剂(CFA)致敏的LEW----(LEW×F-344)F1----(LEW×P2)F1,以及从用BP-CFA致敏的LEW----(LEW×F344)F1----(LEW×F-344)F1进行连续转移,结果在二级受体的脾脏中产生了能够将疾病转移至正常LEW受体的对BP敏感的细胞。为了直接检测F1动物中可能产生的宿主来源的对BP敏感细胞的发育情况,进行了从LEW----(LEW×ACI)F1----(LEW×ACI)F1的EAE连续转移。当从二级(LEW×ACI)F1受体动物获得的对BP敏感细胞被转移至正常LEW和ACI,或照射后的LEW和ACI动物作为最终受体时,疾病仅成功转移至LEW亲代动物。这些结果表明,被动性EAE的发生完全归因于源自主动免疫供体的转移而来的对BP敏感的细胞,并且在被动转移的EAE发病后,没有宿主来源的淋巴细胞被募集到动物脾脏中发现的EAE效应前体细胞池中。

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