• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

通过用抗Vβ8.1,2单克隆抗体进行体内治疗,减轻注射MRL/lpr脾细胞的SCID小鼠的lpr移植物抗宿主病(GVHD)。

Attenuation of lpr-graft-versus-host disease (GVHD) in MRL/lpr spleen cell-injected SCID mice by in vivo treatment with anti-V beta 8.1,2 monoclonal antibody.

作者信息

Hosaka N, Nagata N, Miyashima S, Ikehara S

机构信息

First Department of Pathology, Kansai Medical University, Osaka, Japan.

出版信息

Clin Exp Immunol. 1994 Jun;96(3):500-7. doi: 10.1111/j.1365-2249.1994.tb06057.x.

DOI:10.1111/j.1365-2249.1994.tb06057.x
PMID:8004820
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1534572/
Abstract

When MRL/lpr (H-2k) spleen cells were intraperitoneally injected into C.B-17-scid/scid (severe combined immunodeficient (SCID)) (H-2d) mice, the SCID (SCID-MRL/lpr) mice manifested a severe wasting syndrome with weight loss, splenic atrophy, and lymphoid cell infiltration in the liver and lung, as seen in lpr-GVHD. In contrast, MRL/+ spleen cell-injected SCID (SCID-MRL/+) mice did not show lpr-GVHD. The spleens of SCID-MRL/lpr mice showed progressive increases in donor CD4+ and CD8+ T cells from 4 to 12 weeks after injection and a decrease in B cells at 12 weeks. SCID-MRL/+ mice showed a stable engraftment of CD4+ and CD8+ T cells and a progressive increase in B cells. Analyses of T cell receptor (TCR) repertoires (V beta 6, V beta 8.1,2 and V beta 11) revealed that the V beta 8.1,2+ T cells were found more frequently in SCID-MRL/lpr mice than in SCID-MRL/+ mice. When SCID-MRL/lpr mice were treated with intraperitoneal injection of an anti-V beta 8.1,2 (KJ16) MoAb, V beta 8.1,2+ T cells were markedly depleted, and the severity of lpr-GVHD was attenuated at 4 and 8 weeks after treatment, in contrast to normal rat IgG-injected SCID-MRL/lpr mice. However, the KJ16 MoAb-treated SCID-MRL/lpr mice suffered from severe lpr-GVHD 12 weeks after treatment, although V beta 8.1,2+ T cells were still maintained at a low level. These findings suggest that V beta 8.1,2+ T cells are a major T cell population that mediates lpr-GVHD in the early stage of lpr-GVHD, but that in the later stage, the other T cell populations may proliferate naturally or in accordance with the depletion of V beta 8.1,2+ T cells, and contribute to the development of lpr-GVHD.

摘要

当将MRL/lpr(H-2k)脾细胞腹腔注射到C.B-17-scid/scid(严重联合免疫缺陷(SCID))(H-2d)小鼠体内时,SCID(SCID-MRL/lpr)小鼠表现出严重的消瘦综合征,伴有体重减轻、脾萎缩以及肝脏和肺中的淋巴细胞浸润,这与lpr移植物抗宿主病(GVHD)的表现相同。相比之下,注射MRL/+脾细胞的SCID(SCID-MRL/+)小鼠未表现出lpr-GVHD。SCID-MRL/lpr小鼠的脾脏在注射后4至12周显示供体CD4+和CD8+ T细胞逐渐增加,而在12周时B细胞减少。SCID-MRL/+小鼠显示CD4+和CD8+ T细胞稳定植入,B细胞逐渐增加。对T细胞受体(TCR)库(Vβ6、Vβ8.1、2和Vβ11)的分析表明,与SCID-MRL/+小鼠相比,在SCID-MRL/lpr小鼠中Vβ8.1、2+ T细胞更为常见。当给SCID-MRL/lpr小鼠腹腔注射抗Vβ8.1、2(KJ16)单克隆抗体(MoAb)进行治疗时,Vβ8.1、2+ T细胞明显减少,并且在治疗后4周和8周时lpr-GVHD的严重程度减轻;与之形成对照的是,注射正常大鼠IgG的SCID-MRL/lpr小鼠则不然。然而,尽管Vβ8.1、2+ T细胞仍维持在低水平,但经KJ16 MoAb治疗的SCID-MRL/lpr小鼠在治疗后12周仍患有严重的lpr-GVHD。这些发现表明,Vβ8.1、2+ T细胞是在lpr-GVHD早期介导lpr-GVHD的主要T细胞群体,但在后期,其他T细胞群体可能自然增殖或随着Vβ8.1、2+ T细胞的减少而增殖,并促进lpr-GVHD的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9948/1534572/aff5d340528d/clinexpimmunol00026-0130-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9948/1534572/76fad9f86d26/clinexpimmunol00026-0128-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9948/1534572/aff5d340528d/clinexpimmunol00026-0130-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9948/1534572/76fad9f86d26/clinexpimmunol00026-0128-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9948/1534572/aff5d340528d/clinexpimmunol00026-0130-a.jpg

相似文献

1
Attenuation of lpr-graft-versus-host disease (GVHD) in MRL/lpr spleen cell-injected SCID mice by in vivo treatment with anti-V beta 8.1,2 monoclonal antibody.通过用抗Vβ8.1,2单克隆抗体进行体内治疗,减轻注射MRL/lpr脾细胞的SCID小鼠的lpr移植物抗宿主病(GVHD)。
Clin Exp Immunol. 1994 Jun;96(3):500-7. doi: 10.1111/j.1365-2249.1994.tb06057.x.
2
Analyses of acute graft-versus-host-like reaction in [MRL/lpr----MRL/+] chimeric mice using MRL/lpr-Thy-1. 1 congenic mice.使用MRL/lpr-Thy-1.1同源近交系小鼠对[MRL/lpr----MRL/+]嵌合小鼠的急性移植物抗宿主样反应进行分析。
Cell Immunol. 1991 Oct 1;137(1):189-99. doi: 10.1016/0008-8749(91)90068-m.
3
Auto-MHC class II-reactive T cell line obtained from MRL/+ mice suffering from lpr-GVHD. II. Analyses of functional characteristics of T cell line by in vivo administration.从患有lpr - GVHD的MRL/+小鼠获得的自身MHC II类反应性T细胞系。II. 通过体内给药对T细胞系功能特性的分析。
Immunobiology. 1992 Nov;186(5):339-50. doi: 10.1016/s0171-2985(11)80389-x.
4
MRL/lpr-->severe combined immunodeficiency mouse allografts produce autoantibodies, acute graft-versus-host disease or a wasting syndrome depending on the source of cells.MRL/lpr重度联合免疫缺陷小鼠同种异体移植会产生自身抗体、急性移植物抗宿主病或消瘦综合征,具体取决于细胞来源。
Clin Exp Immunol. 1992 Dec;90(3):466-75. doi: 10.1111/j.1365-2249.1992.tb05869.x.
5
Comparison of wasting syndrome in [MRL lpr/lpr-->MRL +/+] chimera and graft versus host disease in [B10.D2-->BALB/c] chimera and an attempt to transfer the wasting syndrome in [MRL lpr/lpr-->MRL +/+] to MRL +/+ mice.[MRL lpr/lpr→MRL +/+]嵌合体中消瘦综合征与[B10.D2→BALB/c]嵌合体中移植物抗宿主病的比较以及将[MRL lpr/lpr→MRL +/+]中的消瘦综合征转移至MRL +/+小鼠的尝试。
J Dermatol Sci. 1994 Apr;7(2):107-18. doi: 10.1016/0923-1811(94)90084-1.
6
Transfer of Sjögren's syndrome-like autoimmune lesions into SCID mice and prevention of lesions by anti-CD4 and anti-T cell receptor antibody treatment.将干燥综合征样自身免疫性病变转移至重症联合免疫缺陷(SCID)小鼠体内,并通过抗CD4和抗T细胞受体抗体治疗预防病变。
Eur J Immunol. 1994 Nov;24(11):2826-31. doi: 10.1002/eji.1830241137.
7
Analyses of lpr-GVHD by adoptive transfer experiments using MRL/lpr-Thy-1.1 congenic mice.利用MRL/lpr-Thy-1.1同源基因小鼠通过过继转移实验对淋巴细胞性脉络丛脑膜炎病毒相关性移植物抗宿主病进行分析。
Autoimmunity. 1994;17(3):217-24. doi: 10.3109/08916939409010657.
8
Prevention of lpr-graft-versus-host disease and transfer of autoimmune diseases in normal C57BL/6 mice by transplantation of bone marrow cells plus bones (stromal cells) from MRL/lpr mice.通过移植来自MRL/lpr小鼠的骨髓细胞加骨骼(基质细胞)预防正常C57BL/6小鼠的移植物抗宿主病并转移自身免疫性疾病。
J Immunol. 1996 Jan 1;156(1):79-84.
9
Auto-MHC class II-reactive T cell line obtained from MRL/+mice suffering from "lpr-GVHD". I. Characterization of surface phenotypes, specificities and functions in vitro.从患有“lpr - 移植物抗宿主病”的MRL/+小鼠获得的自身MHC II类反应性T细胞系。I. 体外表面表型、特异性和功能的特征分析
Immunobiology. 1990 Nov;181(4-5):367-78. doi: 10.1016/S0171-2985(11)80505-X.
10
Induction of graft versus host disease in SCID mice by MRL/lpr cell transfer.
Clin Immunol Immunopathol. 1994 Jun;71(3):265-72. doi: 10.1006/clin.1994.1085.

引用本文的文献

1
Exuberant expression of chemokine genes by adult human articular chondrocytes in response to IL-1beta.成年人类关节软骨细胞对白细胞介素-1β产生应答时趋化因子基因的过度表达。
Osteoarthritis Cartilage. 2008 Dec;16(12):1560-71. doi: 10.1016/j.joca.2008.04.027. Epub 2008 Jun 18.
2
T-cell receptor Vbeta gene expression in experimental lupus nephritis.实验性狼疮性肾炎中T细胞受体Vβ基因表达
Immunology. 1998 Sep;95(1):18-25. doi: 10.1046/j.1365-2567.1998.00565.x.

本文引用的文献

1
Lack of transfer of lpr-type abnormalities (lymphoproliferation or lymphoid aplasia) in double congenic nude beige mice engrafted with lpr haematopoietic cells.将lpr造血细胞移植到双基因裸米色小鼠中时,lpr型异常(淋巴细胞增殖或淋巴细胞发育不全)未发生转移。
Immunology. 1993 May;79(1):158-66.
2
Determinant spreading and the dynamics of the autoimmune T-cell repertoire.决定簇扩散与自身免疫性T细胞库的动力学
Immunol Today. 1993 May;14(5):203-8. doi: 10.1016/0167-5699(93)90163-F.
3
Molecular cloning and expression of the Fas ligand, a novel member of the tumor necrosis factor family.
肿瘤坏死因子家族新成员Fas配体的分子克隆与表达
Cell. 1993 Dec 17;75(6):1169-78. doi: 10.1016/0092-8674(93)90326-l.
4
A severe combined immunodeficiency mutation in the mouse.小鼠中的一种严重联合免疫缺陷突变。
Nature. 1983 Feb 10;301(5900):527-30. doi: 10.1038/301527a0.
5
Abnormalities induced by the mutant gene Ipr: expansion of a unique lymphocyte subset.由突变基因Ipr诱导的异常:一种独特淋巴细胞亚群的扩增。
J Immunol. 1982 Dec;129(6):2612-5.
6
One-way occurrence of graft-versus-host disease in bone marrow chimaeras between congenic MRL mice.同基因MRL小鼠之间骨髓嵌合体中移植物抗宿主病的单向发生。
Immunology. 1984 Oct;53(2):251-6.
7
Abnormal stem cells in autoimmune-prone mice are responsible for premature thymic involution.自身免疫易感性小鼠中的异常干细胞是胸腺过早退化的原因。
Thymus. 1985;7(3):151-60.
8
Association of lpr gene with graft-vs.-host disease-like syndrome.lpr基因与移植物抗宿主病样综合征的关联。
J Exp Med. 1985 Jul 1;162(1):1-18. doi: 10.1084/jem.162.1.1.
9
Murine models of systemic lupus erythematosus.系统性红斑狼疮的小鼠模型。
Adv Immunol. 1985;37:269-390. doi: 10.1016/s0065-2776(08)60342-9.
10
Cyclosporine-induced autoimmunity. Conditions for expressing disease, requirement for intact thymus, and potency estimates of autoimmune lymphocytes in drug-treated rats.环孢素诱导的自身免疫。药物处理大鼠中疾病表达的条件、完整胸腺的需求以及自身免疫淋巴细胞的效能评估。
J Exp Med. 1986 Nov 1;164(5):1615-25. doi: 10.1084/jem.164.5.1615.