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格雷夫斯病/重症联合免疫缺陷小鼠模型

Graves' disease/model of SCID mouse.

作者信息

Volpé R

机构信息

Division of Endocrinology and Metabolism, University Toronto, Ontario, Canada.

出版信息

Exp Clin Endocrinol Diabetes. 1996;104 Suppl 3:37-40.

PMID:8986420
Abstract

The severe combined immunodeficient (SCID) mouse constitutes an interesting but not ideal model for the study of human Graves' disease (GD) thyroid tissue. While certainly thyroid tissue survives in the SCID mouse, the lymphocytes do not seem to be able to exert their effects in a long term manner as they do in the human host. Primary thyroid xenografts of GD will not remain hyperfunctional, and antibodies seem to subside after several weeks. GD thyroid tissue which has been removed from its immune environment by passing it through the nude mouse for eight weeks, and then re-xenografted in the SCID mouse, will again manifest lymphocytic infiltration only upon injection of autologous human peripheral blood mononuclear cells which thus reconstitute the lesion to some degree. However, we have not been able to reproduce GD by this procedure. We have been able to show organ-specific homing of the autologous peripheral blood lymphocytes to the GD thyroid tissue and a reappearance of histological lymphocytic infiltration, thyrocyte HLA-DR and ICAM-1 expression, and the reappearance of circulating thyroid autoantibodies after injection of autologous peripheral blood mononuclear cells (PBMC). (No such changes occur when normal thyroid tissue is similarly studied). This can be greatly magnified by deleting the CD8 cells prior to (PBMC) injection and can be prevented by adding a surfeit of CD8 cells instead, signifying that this subpopulation of lymphocytes contains suppressor T lymphocytes. The model affords means of studying various immunomodulators in an in vivo situation. Attempts are being made in various centres to more closely simulate GD but it may be necessary to have other mouse models with fewer natural killer (NK) cells to be able to successfully maintain the lymphocytes and tissue in its original state.

摘要

严重联合免疫缺陷(SCID)小鼠是研究人类格雷夫斯病(GD)甲状腺组织的一个有趣但并不理想的模型。虽然甲状腺组织在SCID小鼠中确实能够存活,但淋巴细胞似乎无法像在人类宿主中那样长期发挥作用。GD的原发性甲状腺异种移植不会一直保持高功能状态,抗体在几周后似乎会消退。将GD甲状腺组织通过裸鼠传代八周,使其脱离免疫环境,然后再移植到SCID小鼠中,只有在注射自体人外周血单个核细胞后才会再次出现淋巴细胞浸润,从而在一定程度上重建病变。然而,我们未能通过此程序重现GD。我们已经能够证明自体外周血淋巴细胞向GD甲状腺组织的器官特异性归巢,以及在注射自体外周血单个核细胞(PBMC)后组织学淋巴细胞浸润、甲状腺细胞HLA-DR和ICAM-1表达的再次出现,以及循环甲状腺自身抗体的再次出现。(对正常甲状腺组织进行类似研究时不会出现此类变化)。在注射(PBMC)之前删除CD8细胞可使这种情况大大加剧,而加入过量的CD8细胞则可防止这种情况发生,这表明该淋巴细胞亚群含有抑制性T淋巴细胞。该模型为在体内研究各种免疫调节剂提供了手段。各研究中心正在尝试更紧密地模拟GD,但可能需要有其他自然杀伤(NK)细胞较少的小鼠模型,以便能够成功地将淋巴细胞和组织维持在其原始状态。

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