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人类白细胞抗原系统、抗原加工与呈递

The HLA system, antigen processing and presentation.

作者信息

Krensky A M

机构信息

Department of Pediatrics, Stanford University, California, USA.

出版信息

Kidney Int Suppl. 1997 Mar;58:S2-7.

PMID:9067934
Abstract

Human leukocyte antigens (HLA) restrict immune responses by binding antigenic peptides and presenting them in the context of self to T lymphocytes. In transplantation, a vigorous T cell response, termed alloreactivity, is caused by recognition of non-self HLA. The major histocompatibility complex (MHC) encodes two major classes of HLA molecules, designated I and II. In general, HLA class I molecules present peptides derived by proteolysis of intracellular proteins (the endogenous pathway), while HLA class II molecules present peptides sampled from the extracellular body fluids (the exogenous pathway). The dichotomy between class I and class II antigens is reflected in the T cells in that the CD8 cell surface glycoprotein is expressed by cytotoxic T lymphocytes and recognizes HLA class I, while CD4 is expressed on helper T cells and recognizes HLA class II. Although the two classes of HLA molecules are thought to have originated from a common ancestral gene, they have evolved specific structures and intracellular trafficking compartments that account for their functions. The class I proteins bind short peptides of eight to nine amino acids that are tightly anchored at their ends. The class II proteins bind longer peptides that are more heterogeneous in size (12 to 28 amino acids) and have ragged ends. The class I peptides are generated by proteasomes and other mechanisms in the cytosol and translocated from the cytosol into the endoplasmic reticulum (ER). In the ER, functional HLA class I complexes are formed and then transported to the cell surface for presentation. HLA class II molecules are assembled without antigenic peptide. An "invariant chain" promotes the assembly of the class II molecule and protects its groove from binding peptides in the ER. In an endosomal compartment, antigens that have entered the cell via pinocytosis or via receptor-mediated internalization are processed, the invariant chain is degraded, and antigenic peptides bind to the HLA class II molecule. This mature complex is transported to the cell surface for presentation. Alloreactivity is the special case of antigen presentation responsible for transplant rejection.

摘要

人类白细胞抗原(HLA)通过结合抗原肽并将其在自身背景下呈递给T淋巴细胞来限制免疫反应。在移植过程中,对非自身HLA的识别会引发强烈的T细胞反应,即同种异体反应性。主要组织相容性复合体(MHC)编码两类主要的HLA分子,分别称为I类和II类。一般来说,HLA I类分子呈递通过细胞内蛋白质蛋白水解产生的肽(内源性途径),而HLA II类分子呈递从细胞外体液中获取的肽(外源性途径)。I类和II类抗原之间的二分法在T细胞中有所体现,即细胞毒性T淋巴细胞表达CD8细胞表面糖蛋白并识别HLA I类,而CD4在辅助性T细胞上表达并识别HLA II类。尽管这两类HLA分子被认为起源于一个共同的祖先基因,但它们已经进化出了特定的结构和细胞内运输区室,以实现其功能。I类蛋白结合八到九个氨基酸的短肽,这些短肽在其末端紧密锚定。II类蛋白结合更长的肽,其大小更具异质性(12至28个氨基酸)且末端参差不齐。I类肽由蛋白酶体和胞质溶胶中的其他机制产生,并从胞质溶胶转运到内质网(ER)。在内质网中,功能性HLA I类复合物形成,然后运输到细胞表面进行呈递。HLA II类分子在没有抗原肽的情况下组装。一条“恒定链”促进II类分子的组装,并保护其凹槽在内质网中不与肽结合。在内体区室中,通过胞饮作用或通过受体介导的内化进入细胞的抗原被加工,恒定链被降解,抗原肽与HLA II类分子结合。这种成熟的复合物被运输到细胞表面进行呈递。同种异体反应性是负责移植排斥的抗原呈递的特殊情况。

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