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血吸虫卵肉芽肿巨噬细胞诱导T辅助细胞对抗原无反应性。这是血吸虫病免疫调节的基础吗?

Induction of T helper cell unresponsiveness to antigen by macrophages from schistosomal egg granulomas. A basis for immunomodulation in schistosomiasis?

作者信息

Stadecker M J, Kamisato J K, Chikunguwo S M

机构信息

Department of Pathology, Tufts University School of Medicine, Boston, MA 02111.

出版信息

J Immunol. 1990 Oct 15;145(8):2697-700.

PMID:2145363
Abstract

The present studies were undertaken in an effort to understand the role of mononuclear phagocytes in the regulation of the T cell-mediated granulomatous inflammatory response in experimental murine schistosomiasis mansoni. We report that macrophages from schistosomal egg granulomas did not efficiently stimulate, but rather induced marked proliferative unresponsiveness to Ag in an IL-2-producing, I-Ek-restricted, CD4+ Th cell clone specific for pigeon cytochrome c. The unresponsive state of the T cells was achieved after incubation with granuloma macrophages in the presence of the specific Ag fragment 81-104, but not with either of them independently, and was, similarly, restricted by the I-Ek molecule. Equivalent amounts of peritoneal macrophages from schistosome-infected, but not from normal mice, were also effective in inducing T cell unresponsiveness. We postulate that granuloma macrophages, and potentially other accessory cells in schistosome-infected individuals, are similarly capable of inducing anergy in egg Ag-specific Th cells, and that the resulting inhibited T cell reactivity, which translates into failure of lymphokine secretion and of clonal expansion, represents a major basis of the immunologic down-regulation (immunomodulation) of granulomatous hypersensitivity, characteristically seen in this disease.

摘要

本研究旨在了解单核吞噬细胞在实验性小鼠曼氏血吸虫病中T细胞介导的肉芽肿性炎症反应调节中的作用。我们报告,来自血吸虫卵肉芽肿的巨噬细胞不能有效地刺激,反而在针对鸽细胞色素c的产生白细胞介素-2、受I-Ek限制的CD4 + Th细胞克隆中诱导对Ag的明显增殖无反应性。T细胞的无反应状态是在特异性Ag片段81 - 104存在下与肉芽肿巨噬细胞孵育后实现的,而不是单独与它们中的任何一个孵育,并且同样受I-Ek分子限制。来自感染血吸虫的小鼠而非正常小鼠的等量腹腔巨噬细胞也能有效诱导T细胞无反应性。我们推测,肉芽肿巨噬细胞以及血吸虫感染个体中潜在的其他辅助细胞同样能够诱导卵Ag特异性Th细胞无反应,并且由此产生的T细胞反应性抑制,表现为淋巴因子分泌和克隆扩增失败,是这种疾病中典型的肉芽肿性超敏反应免疫下调(免疫调节)的主要基础。

相似文献

1
Induction of T helper cell unresponsiveness to antigen by macrophages from schistosomal egg granulomas. A basis for immunomodulation in schistosomiasis?血吸虫卵肉芽肿巨噬细胞诱导T辅助细胞对抗原无反应性。这是血吸虫病免疫调节的基础吗?
J Immunol. 1990 Oct 15;145(8):2697-700.
2
Macrophages from schistosomal egg granulomas induce unresponsiveness in specific cloned Th-1 lymphocytes in vitro and down-regulate schistosomal granulomatous disease in vivo.来自血吸虫卵肉芽肿的巨噬细胞在体外可诱导特定克隆的Th-1淋巴细胞产生无反应性,并在体内下调血吸虫性肉芽肿病。
J Immunol. 1994 Feb 15;152(4):1847-55.
3
Role of IL-10 on antigen-presenting cell function for schistosomal egg-specific monoclonal T helper cell responses in vitro and in vivo.白细胞介素-10在体外和体内对血吸虫卵特异性单克隆辅助性T细胞应答的抗原呈递细胞功能中的作用
J Immunol. 1993 Sep 15;151(6):3192-8.
4
The cell-mediated response to schistosomal antigens at the clonal level. In vivo functions of cloned murine egg antigen-specific CD4+ T helper type 1 lymphocytes.克隆水平上对血吸虫抗原的细胞介导反应。克隆的鼠卵抗原特异性CD4+ 1型辅助性T淋巴细胞的体内功能。
J Immunol. 1991 Dec 1;147(11):3921-5.
5
Regulation of T helper cell responses in experimental murine schistosomiasis by IL-10. Effect on expression of B7 and B7-2 costimulatory molecules by macrophages.IL-10 对实验性小鼠血吸虫病中辅助性 T 细胞反应的调节。对巨噬细胞 B7 和 B7-2 共刺激分子表达的影响。
J Immunol. 1994 Dec 1;153(11):5190-9.
6
In infection with Schistosoma mansoni, B cells are required for T helper type 2 cell responses but not for granuloma formation.在曼氏血吸虫感染中,2型辅助性T细胞反应需要B细胞参与,但肉芽肿形成则不需要。
J Immunol. 1997 May 15;158(10):4832-7.
7
Schistosoma mansoni: genetic restriction and cytokine profile of the CD4 + T helper cell response to dominant epitope peptide of major egg antigen Sm-p40.曼氏血吸虫:CD4 + T辅助细胞对主要虫卵抗原Sm-p40优势表位肽反应的遗传限制和细胞因子谱
Exp Parasitol. 1998 Sep;90(1):122-30. doi: 10.1006/expr.1998.4309.
8
Expression of class II, but not class I, major histocompatibility complex molecules is required for granuloma formation in infection with Schistosoma mansoni.曼氏血吸虫感染中肉芽肿形成需要Ⅱ类主要组织相容性复合体分子的表达,而不需要Ⅰ类分子的表达。
Eur J Immunol. 1997 May;27(5):1170-6. doi: 10.1002/eji.1830270518.
9
T cell clones for antigen selection and lymphokine production in murine Schistosomiasis mansoni.用于小鼠曼氏血吸虫病抗原选择和淋巴因子产生的T细胞克隆
J Immunol. 1990 Apr 1;144(7):2757-62.
10
The cell-mediated response to schistosomal antigens at the clonal level. III. Identification of soluble egg antigens recognized by cloned specific granulomagenic murine CD4+ Th1-type lymphocytes.
J Immunol. 1993 Feb 15;150(4):1413-21.

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Induction and regulation of pathogenic Th17 cell responses in schistosomiasis.血吸虫病中致病性 Th17 细胞反应的诱导和调节。
Semin Immunopathol. 2012 Nov;34(6):873-88. doi: 10.1007/s00281-012-0341-9. Epub 2012 Oct 25.
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Th2 cell hyporesponsiveness during chronic murine schistosomiasis is cell intrinsic and linked to GRAIL expression.
慢性小鼠血吸虫病期间Th2细胞低反应性是细胞内在性的,且与GRAIL表达相关。
J Clin Invest. 2009 Apr;119(4):1019-28. doi: 10.1172/JCI36534. Epub 2009 Mar 2.
4
IL-10 and TGF-beta redundantly protect against severe liver injury and mortality during acute schistosomiasis.白细胞介素-10和转化生长因子-β在急性血吸虫病期间对严重肝损伤和死亡具有冗余性保护作用。
J Immunol. 2008 Nov 15;181(10):7214-20. doi: 10.4049/jimmunol.181.10.7214.
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The Schistosoma mansoni hepatic egg granuloma provides a favorable microenvironment for sustained growth of Leishmania donovani.曼氏血吸虫肝虫卵肉芽肿为杜氏利什曼原虫的持续生长提供了有利的微环境。
Am J Pathol. 2006 Sep;169(3):943-53. doi: 10.2353/ajpath.2006.051319.
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Regulation of granulomatous inflammation in experimental models of schistosomiasis.血吸虫病实验模型中肉芽肿性炎症的调节
Infect Immun. 2004 Jan;72(1):1-12. doi: 10.1128/IAI.72.1.1-12.2004.
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Skin-stage schistosomula of Schistosoma mansoni produce an apoptosis-inducing factor that can cause apoptosis of T cells.曼氏血吸虫的皮肤期童虫产生一种可导致T细胞凋亡的凋亡诱导因子。
J Biol Chem. 2002 Sep 13;277(37):34329-35. doi: 10.1074/jbc.M201344200. Epub 2002 Jul 9.
8
Schistosomiasis. Infection versus disease and hypersensitivity versus immunity.血吸虫病:感染与疾病、超敏反应与免疫
Am J Pathol. 1993 Mar;142(3):699-702.
9
Cloning of TH0- and TH2-type helper lymphocytes from liver granulomas of Schistosoma mansoni-infected mice.从曼氏血吸虫感染小鼠肝脏肉芽肿中克隆TH0型和TH2型辅助淋巴细胞。
Infect Immun. 1994 Mar;62(3):994-9. doi: 10.1128/iai.62.3.994-999.1994.
10
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Immunol Res. 1993;12(1):48-64. doi: 10.1007/BF02918368.