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链球菌致热(红斑)毒素A的主要组织相容性复合体II类结合位点。

Major histocompatibility complex class II binding site for streptococcal pyrogenic (erythrogenic) toxin A.

作者信息

Hartwig U F, Gerlach D, Fleischer B

机构信息

First Department of Medicine, University of Mainz, Germany.

出版信息

Med Microbiol Immunol. 1994 Nov;183(5):257-64. doi: 10.1007/BF00198459.

DOI:10.1007/BF00198459
PMID:7715537
Abstract

Streptococcal pyrogenic exotoxin A (SPEA) is an important pathogenicity factor of group A streptococci. It is a member of the family of "superantigens" produced by Staphylococcus aureus and Streptococcus pyogenes and its T lymphocyte stimulating activity is involved into the pathogenesis of certain diseases caused by pyogenic streptococci. In this study we have produced and characterized recombinant SPEA molecules in Escherichia coli. These molecules are indistinguishable from natural SPEA in both T cell stimulatory and HLA class II binding activities. Human class II molecules are more efficient than mouse class II molecules in presenting SPEA to T cells. In binding tests to major histocompatibility complex class II-positive cells SPEA competes with staphylococcal enterotoxin B and A but not with toxic shock syndrome toxin-1.

摘要

A组链球菌致热外毒素A(SPEA)是A组链球菌的一种重要致病因子。它是由金黄色葡萄球菌和化脓性链球菌产生的“超抗原”家族的成员,其T淋巴细胞刺激活性参与了化脓性链球菌引起的某些疾病的发病机制。在本研究中,我们在大肠杆菌中产生并鉴定了重组SPEA分子。这些分子在T细胞刺激活性和HLA-II类结合活性方面与天然SPEA没有区别。人类II类分子在将SPEA呈递给T细胞方面比小鼠II类分子更有效。在与主要组织相容性复合体II类阳性细胞的结合试验中,SPEA与葡萄球菌肠毒素B和A竞争,但不与中毒性休克综合征毒素-1竞争。

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引用本文的文献

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Structural basis for the recognition of superantigen streptococcal pyrogenic exotoxin A (SpeA1) by MHC class II molecules and T-cell receptors.MHC II类分子和T细胞受体识别超抗原链球菌致热外毒素A(SpeA1)的结构基础。
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2
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3
Analysis of the superantigenic activity of mutant and allelic forms of streptococcal pyrogenic exotoxin A.

本文引用的文献

1
Stimulation of human T cells by streptococcal "superantigen" erythrogenic toxins (scarlet fever toxins).链球菌“超抗原”致热外毒素(猩红热毒素)对人T细胞的刺激作用。
J Immunol. 1993 Mar 15;150(6):2457-66.
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Superantigens.超抗原
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Three-dimensional structure of a human class II histocompatibility molecule complexed with superantigen.与超抗原复合的人类II类组织相容性分子的三维结构。
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Human B cell variants immunoselected against a single Ia antigen subset have lost expression of several Ia antigen subsets.针对单个Ia抗原亚群进行免疫选择的人B细胞变体已失去了几个Ia抗原亚群的表达。
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Nucleotide sequence of the enterotoxin B gene from Staphylococcus aureus.金黄色葡萄球菌肠毒素B基因的核苷酸序列。
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Nucleotide sequence of the type A streptococcal exotoxin (erythrogenic toxin) gene from Streptococcus pyogenes bacteriophage T12.化脓性链球菌噬菌体T12的A型链球菌外毒素(致热外毒素)基因的核苷酸序列。
Infect Immun. 1986 Apr;52(1):144-50. doi: 10.1128/iai.52.1.144-150.1986.
8
T cell stimulation by staphylococcal enterotoxins. Clonally variable response and requirement for major histocompatibility complex class II molecules on accessory or target cells.葡萄球菌肠毒素对T细胞的刺激。克隆可变反应以及辅助细胞或靶细胞上主要组织相容性复合体II类分子的需求。
J Exp Med. 1988 May 1;167(5):1697-707. doi: 10.1084/jem.167.5.1697.
9
Purification and characterization of Streptococcus pyogenes erythrogenic toxin type A produced by a cloned gene in Streptococcus sanguis.由血链球菌中克隆基因产生的化脓性链球菌A 型致热外毒素的纯化与特性分析
Zentralbl Bakteriol Mikrobiol Hyg A. 1987 Oct;266(3-4):347-58. doi: 10.1016/s0176-6724(87)80215-8.
10
Single-step purification of polypeptides expressed in Escherichia coli as fusions with glutathione S-transferase.以谷胱甘肽S-转移酶融合形式在大肠杆菌中表达的多肽的一步纯化。
Gene. 1988 Jul 15;67(1):31-40. doi: 10.1016/0378-1119(88)90005-4.