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正常及自身免疫小鼠中白细胞介素2和集落刺激因子产生细胞的有限稀释分析

Limiting dilution analysis of interleukin 2 and colony-stimulating factor producer cells in normal and autoimmune mice.

作者信息

Hefeneider S H, Conlon P J, Dower S K, Henney C S, Gillis S

出版信息

J Immunol. 1984 Apr;132(4):1863-8.

PMID:6607951
Abstract

MRL/MP lpr-lpr (MRL-lpr) mice spontaneously develop an age-related disease characteristic of human systemic lupus erythematosus (SLE). Old MRL-lpr mice (4 mo of age) develop antibodies to nucleic acids, display immune complex glomerulonephritis, and have a massive T cell-associated lymphadenopathy. In concert with disease development is data showing an age-related loss of interleukin 2 (IL 2) production by mitogen-stimulated lymphoid cells from these mice. The loss of IL 2 production has been suggested to be involved in the onset and/or development of autoimmune disease seen in these animals. In this report, we examined the frequency of both IL 2 and colony-stimulating factor (CSF) producer T cells in the MRL-lpr mouse by using a limiting dilution analysis assay. Our results show that the number of IL 2 and CSF producer cells present in autoimmune animals is similar to the number found in normal control mice. In addition, IL 2 and CSF producer T cells from autoimmune MRL-lpr mice make similar levels of lymphokine activity, as do producer T cells from normal mice. Our data argue against the previously hypothesized role that a paucity of IL 2 production may be involved in the etiology of autoimmune disease.

摘要

MRL/MP lpr-lpr(MRL-lpr)小鼠会自发发展出一种具有人类系统性红斑狼疮(SLE)特征的与年龄相关的疾病。老年MRL-lpr小鼠(4月龄)会产生针对核酸的抗体,表现出免疫复合物性肾小球肾炎,并伴有大量与T细胞相关的淋巴结病。与疾病发展相一致的是,有数据表明这些小鼠经丝裂原刺激的淋巴细胞产生白细胞介素2(IL-2)的能力会随着年龄增长而丧失。IL-2产生能力的丧失被认为与这些动物中出现的自身免疫性疾病的发生和/或发展有关。在本报告中,我们通过使用有限稀释分析测定法检测了MRL-lpr小鼠中产生IL-2和集落刺激因子(CSF)的T细胞的频率。我们的结果表明,自身免疫动物中产生IL-2和CSF的细胞数量与正常对照小鼠中的数量相似。此外,来自自身免疫性MRL-lpr小鼠的产生IL-2和CSF的T细胞产生的淋巴因子活性水平与正常小鼠的产生细胞相似。我们的数据反驳了先前假设的观点,即IL-2产生不足可能参与自身免疫性疾病的病因。

相似文献

1
Limiting dilution analysis of interleukin 2 and colony-stimulating factor producer cells in normal and autoimmune mice.正常及自身免疫小鼠中白细胞介素2和集落刺激因子产生细胞的有限稀释分析
J Immunol. 1984 Apr;132(4):1863-8.
2
Signals required for activation and growth of autoimmune T lymphocytes.自身免疫性T淋巴细胞激活和生长所需的信号。
J Mol Cell Immunol. 1984;1(6):347-56.
3
Spontaneous production of interleukin 3 by T lymphocytes from autoimmune MRL/MP-lpr/lpr mice.来自自身免疫性MRL/MP-lpr/lpr小鼠的T淋巴细胞自发产生白细胞介素3 。
Eur J Immunol. 1984 Jul;14(7):599-605. doi: 10.1002/eji.1830140704.
4
T cells from autoimmune "IL 2-defective" MRL-lpr/lpr mice continue to grow in vitro and produce IL 2 constitutively.来自自身免疫性“白细胞介素2缺陷型”MRL-lpr/lpr小鼠的T细胞在体外持续生长并组成性地产生白细胞介素2。
J Immunol. 1984 Nov;133(5):2545-8.
5
Autoreactivity accelerates the development of autoimmunity and lymphoproliferation in MRL/Mp-lpr/lpr mice.自身反应性加速了MRL/Mp-lpr/lpr小鼠自身免疫和淋巴细胞增殖的发展。
J Immunol. 1987 Aug 1;139(3):734-42.
6
The cellular basis for immune interferon production in autoimmune MRL-Ipr/Ipr mice.自身免疫性MRL-Ipr/Ipr小鼠中免疫干扰素产生的细胞基础。
J Immunol. 1983 Jul;131(1):265-8.
7
Autoimmune MRL/lpr mice sera contain IgG with interleukin 3-like activity.
J Immunol. 1988 Jan 15;140(2):520-5.
8
Dissociation of severe lupus-like disease from polyclonal B cell activation and IL 2 deficiency in C3H-lpr/lpr mice.C3H-lpr/lpr小鼠中严重狼疮样疾病与多克隆B细胞激活及白细胞介素2缺乏的解离
J Immunol. 1984 Aug;133(2):1048-56.
9
Responses of B cells from autoimmune mice to IL-5.自身免疫小鼠的B细胞对白细胞介素-5的反应。
J Immunol. 1989 Mar 1;142(5):1528-35.
10
Interleukin 2 is a proliferative signal for B cells from autoimmune mice.白细胞介素2是来自自身免疫小鼠的B细胞的增殖信号。
Eur J Immunol. 1986 Sep;16(9):1105-10. doi: 10.1002/eji.1830160913.

引用本文的文献

1
Influence of early or late dietary restriction on life span and immunological parameters in MRL/Mp-lpr/lpr mice.早期或晚期饮食限制对MRL/Mp-lpr/lpr小鼠寿命和免疫参数的影响。
Proc Natl Acad Sci U S A. 1984 Sep;81(18):5831-5. doi: 10.1073/pnas.81.18.5831.
2
Differential gene expression in autoimmune mice.自身免疫小鼠中的基因差异表达。
Surv Immunol Res. 1985;4(1):48-64. doi: 10.1007/BF02918586.
3
The effect of iron (Fe3+) on the cloning efficiency of human memory T4+ lymphocytes.铁(Fe3+)对人记忆性T4+淋巴细胞克隆效率的影响。
Clin Exp Immunol. 1986 Nov;66(2):340-7.
4
Systemic mononuclear-cell vasculitis in MRL/Mp-lpr/lpr mice. A histologic and immunocytochemical analysis.MRL/Mp-lpr/lpr小鼠的系统性单核细胞性血管炎。组织学和免疫细胞化学分析。
Am J Pathol. 1987 May;127(2):229-42.
5
Synergistic induction by calcium ionophore and phorbol ester of interleukin-2 (IL-2) receptor expression, IL-2 production, and proliferation in autoimmune MRL/MP-lpr mice.钙离子载体与佛波酯协同诱导自身免疫性MRL/MP-lpr小鼠白细胞介素-2(IL-2)受体表达、IL-2产生及增殖
Immunology. 1986 Sep;59(1):43-9.
6
The effect of experimental iron-overload on splenic T cell function: analysis using cloning techniques.实验性铁过载对脾脏T细胞功能的影响:采用克隆技术进行分析
Clin Exp Immunol. 1987 May;68(2):375-83.
7
A new T cell subset expressing B220 and CD4 in lpr mice: defects in the response to mitogens and in the production of IL-2.lpr小鼠中表达B220和CD4的新型T细胞亚群:对丝裂原反应及白细胞介素-2产生存在缺陷
Clin Exp Immunol. 1988 Oct;74(1):36-40.