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恶性贫血中的分子靶点。

Molecular targets in pernicious anaemia.

作者信息

Gleeson P A, Toh B H

机构信息

Department of Pathology and Immunology, Monash University Medical School, Prahran, Victoria, Australia.

出版信息

Immunol Today. 1991 Jul;12(7):233-8. doi: 10.1016/0167-5699(91)90036-S.

DOI:10.1016/0167-5699(91)90036-S
PMID:1653572
Abstract

Autoimmune gastritis, leading to pernicious anaemia, is an organ-specific autoimmune disease characterized by chronic atrophic gastritis and circulating gastric parietal cell autoantibodies. The parietal cell autoantigens have recently been identified as the alpha and beta subunit of the gastric proton pump (H+, K+ ATPase). Here Paul Gleeson and Ban-Hock Toh discuss how the identification of these gastric parietal cell autoantigens and the development of a mouse model of autoimmune gastritis have paved the way for an understanding of the pathogenesis of the gastric lesion.

摘要

自身免疫性胃炎可导致恶性贫血,是一种器官特异性自身免疫性疾病,其特征为慢性萎缩性胃炎和循环胃壁细胞自身抗体。胃壁细胞自身抗原最近已被鉴定为胃质子泵(H⁺,K⁺ ATP酶)的α和β亚基。在此,保罗·格利森和陈万福讨论了这些胃壁细胞自身抗原的鉴定以及自身免疫性胃炎小鼠模型的建立如何为理解胃部病变的发病机制铺平了道路。

相似文献

1
Molecular targets in pernicious anaemia.恶性贫血中的分子靶点。
Immunol Today. 1991 Jul;12(7):233-8. doi: 10.1016/0167-5699(91)90036-S.
2
Animal models of human disease: experimental autoimmune gastritis--a model for autoimmune gastritis and pernicious anemia.人类疾病的动物模型:实验性自身免疫性胃炎——自身免疫性胃炎和恶性贫血的模型
Clin Immunol. 2002 Jan;102(1):48-58. doi: 10.1006/clim.2001.5134.
3
The parietal cell autoantigens recognized in neonatal thymectomy-induced murine gastritis are the alpha and beta subunits of the gastric proton pump [corrected].在新生期胸腺切除诱导的小鼠胃炎中识别出的壁细胞自身抗原是胃质子泵的α和β亚基[已修正]。
Gastroenterology. 1991 Aug;101(2):287-94. doi: 10.1016/0016-5085(91)90002-3.
4
Monoclonal antibodies specific for the core protein of the beta-subunit of the gastric proton pump (H+/K+ ATPase). An autoantigen targetted in pernicious anaemia.针对胃质子泵(H⁺/K⁺ATP酶)β亚基核心蛋白的单克隆抗体。这是恶性贫血中的一个自身抗原靶点。
Eur J Biochem. 1991 Apr 10;197(1):49-59. doi: 10.1111/j.1432-1033.1991.tb15881.x.
5
HL-A3 and HL-A7 in pernicious anaemia and autoimmune atrophic gastritis.恶性贫血和自身免疫性萎缩性胃炎中的HL - A3和HL - A7。
Clin Exp Immunol. 1975 Oct;22(1):47-53.
6
Characterization of antigenic structures in auto-immune atrophic gastritis with pernicious anaemia. The parietal cell H,K-ATPase and the chief cell pepsinogen are the two major antigens.伴有恶性贫血的自身免疫性萎缩性胃炎中抗原结构的特征。壁细胞H,K-ATP酶和主细胞胃蛋白酶原是两种主要抗原。
Acta Physiol Scand. 1989 Aug;136(4):581-7. doi: 10.1111/j.1748-1716.1989.tb08705.x.
7
Murine experimental autoimmune gastritis models refractive to development of intrinsic factor autoantibodies, cobalamin deficiency and pernicious anemia.对内因子自身抗体产生、钴胺素缺乏和恶性贫血发展具有抗性的小鼠实验性自身免疫性胃炎模型。
Clin Immunol. 2007 Jan;122(1):41-52. doi: 10.1016/j.clim.2006.08.013. Epub 2006 Oct 10.
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Immune aspects of pernicious anaemia and atrophic gastritis.恶性贫血和萎缩性胃炎的免疫方面
Clin Haematol. 1976 Oct;5(3):497-519.
9
Expression of a gastric autoantigen in pancreatic islets results in non-destructive insulitis after neonatal thymectomy.胰腺胰岛中胃自身抗原的表达在新生期胸腺切除术后导致非破坏性胰岛炎。
Eur J Immunol. 1995 Sep;25(9):2686-94. doi: 10.1002/eji.1830250943.
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Experimental autoimmune gastritis: mouse models of human organ-specific autoimmune disease.实验性自身免疫性胃炎:人类器官特异性自身免疫性疾病的小鼠模型
Int Rev Immunol. 2005 Jan-Apr;24(1-2):93-110. doi: 10.1080/08830180590884585.

引用本文的文献

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Intrinsic factor recognition promotes T helper 17/T helper 1 autoimmune gastric inflammation in patients with pernicious anemia.内因子识别会促进恶性贫血患者的辅助性T细胞17/辅助性T细胞1自身免疫性胃炎。
Oncotarget. 2019 Apr 23;10(30):2921-2929. doi: 10.18632/oncotarget.26874.
2
Th1, Th2, and Th17 effector T cell-induced autoimmune gastritis differs in pathological pattern and in susceptibility to suppression by regulatory T cells.Th1、Th2和Th17效应T细胞诱导的自身免疫性胃炎在病理模式以及对调节性T细胞抑制的易感性方面存在差异。
J Immunol. 2008 Aug 1;181(3):1908-16. doi: 10.4049/jimmunol.181.3.1908.
3
Protective role of interleukin-10-producing regulatory dendritic cells against murine autoimmune gastritis.
产生白细胞介素-10的调节性树突状细胞对小鼠自身免疫性胃炎的保护作用。
J Gastroenterol. 2008;43(2):100-7. doi: 10.1007/s00535-007-2133-x. Epub 2008 Feb 29.
4
A novel and effective approach of developing aggressive experimental autoimmune gastritis in neonatal thymectomized BALB/c mouse by polyinosinic:polycytidylic acid.一种通过聚肌苷酸:聚胞苷酸在新生期胸腺切除的BALB/c小鼠中诱导侵袭性实验性自身免疫性胃炎的新颖且有效的方法。
Clin Exp Immunol. 2004 Jun;136(3):423-31. doi: 10.1111/j.1365-2249.2004.02467.x.
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Immunologic self-tolerance maintained by CD25(+)CD4(+) regulatory T cells constitutively expressing cytotoxic T lymphocyte-associated antigen 4.由持续表达细胞毒性T淋巴细胞相关抗原4的CD25(+)CD4(+)调节性T细胞维持的免疫自身耐受性。
J Exp Med. 2000 Jul 17;192(2):303-10. doi: 10.1084/jem.192.2.303.
6
Identification of a gastritogenic epitope of the H/K ATPase beta-subunit.胃/钾ATP酶β亚基致胃炎表位的鉴定
Immunology. 1999 Jan;96(1):145-51. doi: 10.1046/j.1365-2567.1999.00669.x.
7
Spontaneous autoimmune gastritis in C3H/He mice: a new mouse model for gastric autoimmunity.C3H/He小鼠的自发性自身免疫性胃炎:一种新的胃自身免疫小鼠模型。
Am J Pathol. 1998 Oct;153(4):1311-8. doi: 10.1016/S0002-9440(10)65676-3.
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CD4+ T cells, but not CD8+ T cells, are required for the development of experimental autoimmune gastritis.实验性自身免疫性胃炎的发生需要CD4 + T细胞而非CD8 + T细胞。
Immunology. 1998 Mar;93(3):405-8. doi: 10.1046/j.1365-2567.1998.00436.x.
9
Immunization with gastric H+/K(+)-ATPase induces a reversible autoimmune gastritis.用胃H⁺/K⁺-ATP酶进行免疫会引发一种可逆性自身免疫性胃炎。
Immunology. 1997 Sep;92(1):91-8. doi: 10.1046/j.1365-2567.1997.00302.x.
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An autoimmune disease with multiple molecular targets abrogated by the transgenic expression of a single autoantigen in the thymus.一种自身免疫性疾病,其多个分子靶点因胸腺中单一自身抗原的转基因表达而被消除。
J Exp Med. 1993 Aug 1;178(2):419-26. doi: 10.1084/jem.178.2.419.