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由于主要组织相容性复合体I类和II类差异而发生移植物抗宿主反应的小鼠中巨噬细胞的免疫抑制活性。

Immunosuppressive activity of macrophages in mice undergoing graft-versus-host reaction due to major histocompatibility complex class I plus II difference.

作者信息

Ikarashi Y, Kawai K, Watanabe H, Matsumoto Y, Omata S, Fujiwara M

机构信息

Department of Biosystem Science, Graduate School of Science and Technology, Niigata University, Japan.

出版信息

Immunology. 1993 May;79(1):95-102.

PMID:8099568
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1422042/
Abstract

In a previous report, we showed that the injection of parental CD4+ T cells into major histocompatibility complex (MHC) class II disparate F1 hybrid mice induces autoimmune-like graft versus-host reaction (GVHR) resembling systemic lupus erythematosus (SLE) and the hepatic lesion of primary biliary cirrhosis (PBC). In the present study, we examined whether or not simultaneous or subsequent injection of CD8+ T cells changes the GVHR form. When parental CD8+ T cells together with CD4+ T cells were injected into MHC class I plus class II-disparate F1 mice, autoimmune phenomena did not develop and alternatively a profound immunosuppressive state was induced. Furthermore, ongoing autoimmune-like GVHR induced by CD4+ T cells was also suppressed by later injection of CD8+ T cells. In these mice, an increase of donor type CD8+ T cells and a marked decrease of host B and T cells in the spleen were observed. The spleen cells from these mice strongly inhibited the mitogenic response of normal spleen cells against lipopolysaccharide (LPS). In vitro studies demonstrated that this immunosuppression was not induced by CD8+ T cells themselves but by macrophages which produced suppressive factor(s) by LPS stimulation. These findings were discussed with reference to suppressive mechanisms of GVHR.

摘要

在之前的一份报告中,我们表明将亲代CD4+ T细胞注射到主要组织相容性复合体(MHC)II类不相容的F1杂交小鼠中会诱发类似自身免疫的移植物抗宿主反应(GVHR),类似于系统性红斑狼疮(SLE)和原发性胆汁性肝硬化(PBC)的肝脏病变。在本研究中,我们检测了同时或随后注射CD8+ T细胞是否会改变GVHR的形式。当将亲代CD8+ T细胞与CD4+ T细胞一起注射到MHC I类加II类不相容的F1小鼠中时,并未出现自身免疫现象,相反,诱导出了一种深度免疫抑制状态。此外,后期注射CD8+ T细胞也抑制了由CD4+ T细胞诱导的正在进行的类似自身免疫的GVHR。在这些小鼠中,观察到脾脏中供体类型CD8+ T细胞增加,宿主B细胞和T细胞显著减少。这些小鼠的脾细胞强烈抑制正常脾细胞对脂多糖(LPS)的促有丝分裂反应。体外研究表明,这种免疫抑制不是由CD8+ T细胞本身诱导的,而是由经LPS刺激产生抑制因子的巨噬细胞诱导的。结合GVHR的抑制机制对这些发现进行了讨论。

相似文献

1
Immunosuppressive activity of macrophages in mice undergoing graft-versus-host reaction due to major histocompatibility complex class I plus II difference.由于主要组织相容性复合体I类和II类差异而发生移植物抗宿主反应的小鼠中巨噬细胞的免疫抑制活性。
Immunology. 1993 May;79(1):95-102.
2
Mechanism of the induction of autoimmune disease by graft-versus-host reaction. Role of CD8+ cells in the development of hepatic and ductal lesions induced by CD4+ cells in MHC class I plus II-different host.移植物抗宿主反应诱导自身免疫性疾病的机制。在 MHC I 类和 II 类不同宿主中,CD8 + 细胞在由 CD4 + 细胞诱导的肝脏和导管病变发展中的作用。
Lab Invest. 1994 May;70(5):609-19.
3
Depletion of CD8+ cells exacerbates organ-specific autoimmune diseases induced by CD4+ T cells in semiallogeneic hosts with MHC class II disparity.在具有MHC II类差异的半同种异体宿主中,CD8 +细胞的耗竭会加剧由CD4 + T细胞诱导的器官特异性自身免疫性疾病。
J Immunol. 1990 Nov 15;145(10):3268-75.
4
Role of L3T4+ and Lyt-2+ donor cells in graft-versus-host immune deficiency induced across a class I, class II, or whole H-2 difference.L3T4+和Lyt-2+供体细胞在跨越I类、II类或整个H-2差异诱导的移植物抗宿主免疫缺陷中的作用。
J Immunol. 1988 Apr 15;140(8):2600-8.
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Isolated peripheral T cells from GvHR recipients exhibit defective IL-2R expression, IL-2 production, and proliferation in response to activation stimuli.来自移植物抗宿主反应(GvHR)受体的分离外周血T细胞在受到激活刺激后,表现出白细胞介素-2受体(IL-2R)表达缺陷、白细胞介素-2(IL-2)产生缺陷以及增殖缺陷。
J Immunol. 1990 Dec 15;145(12):3998-4005.
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GVHR elicited by products of class I or class II loci of the MHC: analysis of the response of mouse T lymphocytes to products of class I and class II loci of the MHC in correlation with GVHR-induced mortality, medullary aplasia, and enteropathy.由主要组织相容性复合体(MHC)I类或II类基因座产物引发的移植物抗宿主反应(GVHR):分析小鼠T淋巴细胞对MHC I类和II类基因座产物的反应与GVHR诱导的死亡率、骨髓发育不全和肠病的相关性。
J Immunol. 1985 Sep;135(3):1637-43.
7
Repopulation of host lymphohematopoietic systems by donor cells during graft-versus-host reaction in unirradiated adult F1 mice injected with parental lymphocytes.在未受照射的成年F1小鼠中注射亲代淋巴细胞后,移植物抗宿主反应期间供体细胞对宿主淋巴造血系统的再填充。
J Immunol. 1991 Apr 1;146(7):2108-15.
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Activation of CD4+ and CD8+ lymphocyte subsets by streptozotocin in the popliteal lymph node assay. II. Comparison with acute graft-vs-host reaction in H-2 incompatible F1 mouse hybrids.在腘窝淋巴结试验中链脲佐菌素对CD4 +和CD8 +淋巴细胞亚群的激活作用。II. 与H-2不相容F1小鼠杂种中的急性移植物抗宿主反应的比较
Immunopharmacol Immunotoxicol. 1992;14(4):865-82. doi: 10.3109/08923979209009239.
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Graft-vs-host reactions (GVHR) across minor murine histocompatibility barriers. II. Development of natural suppressor cell activity.跨越小鼠次要组织相容性屏障的移植物抗宿主反应(GVHR)。II. 天然抑制细胞活性的发展。
J Immunol. 1985 Sep;135(3):1644-51.
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Analysis of immunosuppression generated by the graft-versus-host reaction. II. Characterization of the suppression cell and its mechanism of action.移植物抗宿主反应产生的免疫抑制分析。II. 抑制细胞的特性及其作用机制。
Immunology. 1976 Dec;31(6):943-51.

本文引用的文献

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A systemic lupus erythematosus (SLE)-like disease in mice induced by abnormal T-B cell cooperation. Preferential formation of autoantibodies characteristic of SLE.由异常T细胞与B细胞协作诱导的小鼠系统性红斑狼疮(SLE)样疾病。优先形成SLE特征性自身抗体。
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Diseases caused by reactions of T lymphocytes towards incompatible structures of the major histocompatibility complex. VI. Autoantibodies characteristic of systemic lupus erythematosus induced by abnormal T-B cell cooperation across I-E.由T淋巴细胞对主要组织相容性复合体不相容结构的反应所引起的疾病。VI. 跨I-E的异常T-B细胞协作诱导产生的系统性红斑狼疮特征性自身抗体
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Modulation of F1 cytotoxic potentials by GvHR. Host- and donor-derived cytotoxic lymphocytes arise in the unirradiated F1 host spleens under the condition of GvHR-associated immunosuppression.移植物抗宿主反应对F1细胞毒性潜能的调节。在移植物抗宿主反应相关免疫抑制条件下,宿主和供体来源的细胞毒性淋巴细胞在未受照射的F1宿主脾脏中产生。
J Immunol. 1983 Sep;131(3):1142-8.
4
Allosuppressor and allohelper T cells in acute and chronic graft-vs-host disease. I. Alloreactive suppressor cells rather than killer T cells appear to be the decisive effector cells in lethal graft-vs.-host disease.急性和慢性移植物抗宿主病中的同种抑制性T细胞和同种辅助性T细胞。I. 在致死性移植物抗宿主病中,起决定性作用的效应细胞似乎是同种反应性抑制细胞而非杀伤性T细胞。
J Exp Med. 1982 May 1;155(5):1501-22. doi: 10.1084/jem.155.5.1501.
5
Capacity of genetically different T lymphocytes to induce lethal graft-versus-host disease correlates with their capacity to generate suppression but not with their capacity to generate anti-F1 killer cells. A non-H-2 locus determines the inability to induce lethal graft-versus-host disease.基因不同的T淋巴细胞诱导致死性移植物抗宿主病的能力与其产生抑制作用的能力相关,而与其产生抗F1杀伤细胞的能力无关。一个非H-2基因座决定了无法诱导致死性移植物抗宿主病。
J Exp Med. 1981 Jun 1;153(6):1474-88. doi: 10.1084/jem.153.6.1474.
6
Allosuppressor- and allohelper-T cells in acute and chronic graft-vs.-host (GVH) disease. III. Different Lyt subsets of donor T cells induce different pathological syndromes.急性和慢性移植物抗宿主病(GVH)中的同种抑制性和同种辅助性T细胞。III. 供体T细胞的不同Lyt亚群诱导不同的病理综合征。
J Exp Med. 1983 Aug 1;158(2):546-58. doi: 10.1084/jem.158.2.546.
7
Allosuppressor and allohelper T cells in acute and chronic graft-vs.-host disease. II. F1 recipients carrying mutations at H-2K and/or I-A.急性和慢性移植物抗宿主病中的同种抑制性和同种辅助性T细胞。II. 在H-2K和/或I-A携带突变的F1受体。
J Exp Med. 1983 Feb 1;157(2):755-71. doi: 10.1084/jem.157.2.755.
8
Diseases caused by reactions of T lymphocytes to incompatible structures of the major histocompatibility complex. VII. Immune-complex glomerulonephritis.由T淋巴细胞对主要组织相容性复合体不相容结构的反应所引起的疾病。VII. 免疫复合物肾小球肾炎。
J Immunol. 1983 Jan;130(1):209-15.
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Separation of mouse spleen cells by passage through columns of sephadex G-10.通过葡聚糖凝胶G - 10柱对小鼠脾细胞进行分离。
J Immunol Methods. 1974 Aug;5(3):239-47. doi: 10.1016/0022-1759(74)90108-2.
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A rapid method for the isolation of functional thymus-derived murine lymphocytes.一种分离功能性胸腺来源的小鼠淋巴细胞的快速方法。
Eur J Immunol. 1973 Oct;3(10):645-9. doi: 10.1002/eji.1830031011.