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体内加工的自身抗原的功能识别

Functional recognition of in vivo processed self antigen.

作者信息

Stockinger B, Hausmann B

机构信息

National Institute for Medical Research, Department of Molecular Immunology, Mill Hill, London, UK.

出版信息

Int Immunol. 1994 Feb;6(2):247-54. doi: 10.1093/intimm/6.2.247.

DOI:10.1093/intimm/6.2.247
PMID:8155601
Abstract

C5, the fifth component of complement, is a circulating self protein which induces complete tolerance in MHC class II restricted, CD4+ T cells due to the presentation of C5 taken up from plasma. Functional recognition of in vivo processed C5 was monitored by activation of C5 specific T cell hybrids cultured with antigen presenting cells (APC) from C5 expressing mice. Dendritic cells isolated from various tissues (spleen, thymus, skin) proved to be the most efficient APC, since 10- to 50-fold more macrophages and at least 100- to 500-fold more B cells were needed to achieve similar T cell activation. Stimulatory C5 peptide--class II complexes generated in vivo were retained on the surface of dendritic cells but not on macrophages and B cells upon prolonged culture. Dendritic cells but not macrophages from thymus presented in vivo processed C5. Taken together these findings emphasize the crucial role dendritic cells play for recognition of soluble self proteins by MHC class II restricted T cells.

摘要

补体的第五成分C5是一种循环自身蛋白,由于从血浆中摄取的C5的呈递,它能诱导MHC II类限制性CD4+ T细胞产生完全耐受性。通过用来自表达C5的小鼠的抗原呈递细胞(APC)培养C5特异性T细胞杂交瘤的激活来监测体内加工的C5的功能识别。从各种组织(脾脏、胸腺、皮肤)分离的树突状细胞被证明是最有效的APC,因为需要多10至50倍的巨噬细胞和至少多100至500倍的B细胞才能实现类似的T细胞激活。体内产生的刺激性C5肽-II类复合物在长期培养后保留在树突状细胞表面,而不在巨噬细胞和B细胞表面。胸腺中的树突状细胞而非巨噬细胞呈递体内加工的C5。这些发现共同强调了树突状细胞在MHC II类限制性T细胞识别可溶性自身蛋白中所起的关键作用。

相似文献

1
Functional recognition of in vivo processed self antigen.体内加工的自身抗原的功能识别
Int Immunol. 1994 Feb;6(2):247-54. doi: 10.1093/intimm/6.2.247.
2
Presentation of a circulating self protein (C5) to MHC class II restricted T cells.将循环自身蛋白(C5)呈递给MHC II类限制性T细胞。
Int Rev Immunol. 1993;10(4):357-64. doi: 10.3109/08830189309061710.
3
Mechanisms of tolerance induction in major histocompatibility complex class II-restricted T cells specific for a blood-borne self-antigen.针对一种血源性自身抗原的主要组织相容性复合体II类限制性T细胞中耐受诱导的机制。
J Exp Med. 1994 Dec 1;180(6):2089-99. doi: 10.1084/jem.180.6.2089.
4
Macrophage presentation of endogenous self-protein: the MHC class II presentation pathway is not accessible to intracellular C5 or alpha 1-antitrypsin.巨噬细胞对内源性自身蛋白的呈递:细胞内的C5或α1-抗胰蛋白酶无法通过MHC II类呈递途径。
Cell Immunol. 1996 Feb 1;167(2):230-40. doi: 10.1006/cimm.1996.0031.
5
Capacity of antigen uptake by B cells, fibroblasts or macrophages determines efficiency of presentation of a soluble self antigen (C5) to T lymphocytes.B细胞、成纤维细胞或巨噬细胞摄取抗原的能力决定了可溶性自身抗原(C5)呈递给T淋巴细胞的效率。
Eur J Immunol. 1992 May;22(5):1271-8. doi: 10.1002/eji.1830220523.
6
T cell immunity or tolerance as a consequence of self antigen presentation.由于自身抗原呈递导致的T细胞免疫或耐受。
Eur J Immunol. 1989 Jan;19(1):105-10. doi: 10.1002/eji.1830190117.
7
Antigen-presenting cells in the thymus that can negatively select MHC class II-restricted T cells recognizing a circulating self antigen.胸腺中的抗原呈递细胞可对识别循环自身抗原的MHC II类限制性T细胞进行阴性选择。
J Immunol. 1997 Jan 15;158(2):693-706.
8
Localization of self antigen: implications for antigen presentation and induction of tolerance.自身抗原的定位:对抗原呈递及耐受性诱导的影响
Eur J Immunol. 1993 Jan;23(1):6-11. doi: 10.1002/eji.1830230103.
9
Excessive degradation of intracellular protein in macrophages prevents presentation in the context of major histocompatibility complex class II molecules.巨噬细胞内蛋白质过度降解会妨碍其在主要组织相容性复合体II类分子环境中的呈递。
Eur J Immunol. 1997 Jun;27(6):1506-14. doi: 10.1002/eji.1830270629.
10
Constitutive presentation of dominant epitopes from endogenous naturally processed self-beta 2-microglobulin to class II-restricted T cells leads to self-tolerance.内源性天然加工的自身β2-微球蛋白的显性表位向II类限制性T细胞的组成性呈递导致自身耐受。
J Immunol. 1995 Jan 15;154(2):545-54.

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