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“包膜化”经表皮转移后皮肤朗格汉斯细胞(LC)在HIV-1肽胞质加工及HLA I类分子向CD8+ 细胞毒性T淋巴细胞呈递中的作用分析——一种人类免疫方法

An analysis of the role of skin Langerhans cells (LC) in the cytoplasmic processing of HIV-1 peptides after "peplotion" transepidermal transfer and HLA class I presentation to CD8+ CTLs--an approach to immunization of humans.

作者信息

Becker Y

机构信息

Department of Molecular Virology, Faculty of Medicine, Hebrew University of Jerusalem, Israel.

出版信息

Virus Genes. 1995 Jan;9(2):133-47. doi: 10.1007/BF01702656.

Abstract

Skin Langerhans cells (LC) are antigen-presenting cells capable of expressing MHC class I and class II molecules on the plasma membrane. This molecular activity was reviewed to combine the knowledge of peptide presentation by MHC and HLA class I and class II molecules to prime CD8+ cytotoxic T cells (CTLs) and CD4+ T helper cells, respectively. The possible utilization of the skin dendritic cells for the development of antiviral CTLs and antibodies by synthetic peptides modeled according to the motifs of peptides that naturally interact with the peptide binding grooves of the various HLA haplotypes is discussed and evaluated. It may be possible that the introduction of synthetic viral peptides with motifs to fit the HLA class I haplotypes of a human population to the skin dendritic cells will prime selectively the cellular or the humoral immune responses. This approach may provide a new vaccination technique that applies synthetic virus peptides as vaccines for the immunization of humans. The neuropeptide CGRP interacts with LC and modulates antigen presentation.

摘要

皮肤朗格汉斯细胞(LC)是能够在质膜上表达MHC I类和II类分子的抗原呈递细胞。对这种分子活性进行了综述,以结合MHC以及HLA I类和II类分子呈递肽的知识,分别启动CD8 +细胞毒性T细胞(CTL)和CD4 +辅助性T细胞。讨论并评估了根据与各种HLA单倍型的肽结合槽自然相互作用的肽基序建模的合成肽,利用皮肤树突状细胞开发抗病毒CTL和抗体的可能性。将具有适合人群HLA I类单倍型基序的合成病毒肽引入皮肤树突状细胞可能会选择性地启动细胞免疫或体液免疫反应。这种方法可能提供一种新的疫苗接种技术,将合成病毒肽用作人类免疫的疫苗。神经肽降钙素基因相关肽(CGRP)与LC相互作用并调节抗原呈递。

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