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通过工程化的 I 类抗原呈递分子打破耐受。

Breaking tolerance with engineered class I antigen-presenting molecules.

机构信息

Department of Immunology, Mayo Clinic, Rochester, MN 55905.

Immunology PhD Program, Mayo Clinic Graduate School of Biomedical Sciences, Rochester, MN 55905.

出版信息

Proc Natl Acad Sci U S A. 2019 Feb 19;116(8):3136-3145. doi: 10.1073/pnas.1807465116. Epub 2019 Feb 6.

Abstract

Successful efforts to activate T cells capable of recognizing weak cancer-associated self-antigens have employed altered peptide antigens to activate T cell responses capable of cross-reacting on native tumor-associated self. A limitation of this approach is the requirement for detailed knowledge about the altered self-peptide ligands used in these vaccines. In the current study we considered allorecognition as an approach for activating CTL capable of recognizing weak or self-antigens in the context of self-MHC. Nonself antigen-presenting molecules typically contain polymorphisms that influence interactions with the bound peptide and TCR interface. Recognition of these nonself structures results in peptide-dependent alloimmunity. Alloreactive T cells target their inducing alloantigens as well as third-party alloantigens but generally fail to target self-antigens. Certain residues located on the alpha-1/2 domains of class I antigen-presenting molecules primarily interface with TCR. These residues are more conserved within and across species than are residues that determine peptide antigen binding properties. Class I variants designed with amino acid substitutions at key positions within the conserved helical structures are shown to provide strong activating signals to alloreactive CD8 T cells while avoiding changes in naturally bound peptide ligands. Importantly, CTL activated in this manner can break self-tolerance by reacting to self-peptides presented by native MHC. The ability to activate self-tolerant T cells capable of cross-reacting on self-peptide-MHC in vivo represents an approach for inducing autoimmunity, with possible application in cancer vaccines.

摘要

成功激活能够识别弱肿瘤相关自身抗原的 T 细胞的努力采用了改变的肽抗原来激活能够与天然肿瘤相关自身发生交叉反应的 T 细胞反应。这种方法的一个局限性是需要详细了解这些疫苗中使用的改变的自身肽配体。在当前的研究中,我们将同种异体识别视为一种激活 CTL 的方法,这些 CTL 能够在自身 MHC 的背景下识别弱自身或自身抗原。非自身抗原呈递分子通常含有影响与结合肽和 TCR 界面相互作用的多态性。对这些非自身结构的识别导致肽依赖性同种异体免疫。同种反应性 T 细胞针对其诱导的同种异体抗原以及第三方同种异体抗原,但通常不能针对自身抗原。位于 I 类抗原呈递分子的α-1/2 结构域上的某些残基主要与 TCR 相互作用。这些残基在物种内和跨物种之间比决定肽抗原结合特性的残基更保守。在保守的螺旋结构内的关键位置设计具有氨基酸取代的 I 类变体被证明能够向同种反应性 CD8 T 细胞提供强烈的激活信号,同时避免天然结合的肽配体发生变化。重要的是,以这种方式激活的 CTL 可以通过对天然 MHC 呈递的自身肽反应来打破自身耐受性。激活能够在体内与自身肽-MHC 发生交叉反应的自身耐受 T 细胞的能力代表了一种诱导自身免疫的方法,可能在癌症疫苗中有应用。

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Breaking tolerance with engineered class I antigen-presenting molecules.通过工程化的 I 类抗原呈递分子打破耐受。
Proc Natl Acad Sci U S A. 2019 Feb 19;116(8):3136-3145. doi: 10.1073/pnas.1807465116. Epub 2019 Feb 6.

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