{"title":"Hla和癌症","authors":"Aleksandr S. Golota","doi":"10.36425/rehab79387","DOIUrl":null,"url":null,"abstract":"This review provides updated information on HLA class I and II antigens in cancer. The expression of HLA antigens in normal and tumor tissues, the physiological organization of the components of HLA antigen-processing machinery, the expression patterns of HLA antigens associated with the molecular and regulatory defects identified to date, as well as their functional and clinical significance, are described. This review summarizes clinical and experimental data on the complexity of immune escape mechanisms used by tumour cells to avoid T and natural killer cell responses. The variety of class I HLA phenotypes that can be produced by tumor cells during this process is presented. We also discuss here the potential capacity of metastatic lesions to recover MHC/HLA class I expression after immunotherapy, which depends on the reversible/ soft or irreversible/hard nature of the molecular mechanism responsible for the altered HLA class I phenotypes, and which determines the progression or regression of metastatic lesions in response to treatment. HLA сlass II genes play key roles in connecting innate and adaptive immunity in tumor rejection and when the escape route via HLA-I is already established. Antigens сlass II HLA expression in tumor cells and gives tumor cells the ability to present antigens, becoming less aggressive, and improves prognosis. Malignant tumors, as a genetic disease, are caused by structural alterations of the genome which can give rise to the expression of tumor-associated antigens in the form of either structurally altered molecules or of overexpressed normal molecules. Tumor associated antigens recognized by the immune system and induce a T-cell-mediated immune response. Outgrowing cancers use different strategies to evade destruction by the immune system. Immune evasion mechanisms affecting the expression and/or function of HLA-antigens are of special interest to tumor immunologists, since these molecules play a crucial role in the interaction of malignant cells with immune cells. This review describes the potential role of immunity control points in immunosuppression and therapeutic strategies for restoring the cytotoxicity of immune cells.","PeriodicalId":142894,"journal":{"name":"Physical and rehabilitation medicine, medical rehabilitation","volume":"28 4 Pt 2 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"HLA AND CANCER\",\"authors\":\"Aleksandr S. 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We also discuss here the potential capacity of metastatic lesions to recover MHC/HLA class I expression after immunotherapy, which depends on the reversible/ soft or irreversible/hard nature of the molecular mechanism responsible for the altered HLA class I phenotypes, and which determines the progression or regression of metastatic lesions in response to treatment. HLA сlass II genes play key roles in connecting innate and adaptive immunity in tumor rejection and when the escape route via HLA-I is already established. Antigens сlass II HLA expression in tumor cells and gives tumor cells the ability to present antigens, becoming less aggressive, and improves prognosis. Malignant tumors, as a genetic disease, are caused by structural alterations of the genome which can give rise to the expression of tumor-associated antigens in the form of either structurally altered molecules or of overexpressed normal molecules. 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引用次数: 0
摘要
本文综述了HLA I类和II类抗原在癌症中的最新信息。本文描述了HLA抗原在正常组织和肿瘤组织中的表达,HLA抗原加工机制组成部分的生理组织,HLA抗原的表达模式与迄今为止发现的分子和调节缺陷相关,以及它们的功能和临床意义。本文综述了肿瘤细胞用于避免T细胞和自然杀伤细胞反应的免疫逃逸机制的复杂性的临床和实验数据。在此过程中,肿瘤细胞可产生的I类HLA表型的多样性被提出。我们还讨论了转移性病变在免疫治疗后恢复MHC/HLA I类表达的潜在能力,这取决于导致HLA I类表型改变的分子机制的可逆/软或不可逆/硬性质,并决定了转移性病变在治疗后的进展或消退。当通过HLA- 1的逃避途径已经建立时,HLA- r - II基因在肿瘤排斥反应中连接先天免疫和适应性免疫中发挥关键作用。HLA抗原在肿瘤细胞中的表达,使肿瘤细胞能够呈递抗原,降低侵袭性,改善预后。恶性肿瘤作为一种遗传疾病,是由基因组的结构改变引起的,这种改变会导致肿瘤相关抗原以结构改变的分子或过度表达的正常分子的形式表达。肿瘤相关抗原被免疫系统识别并诱导t细胞介导的免疫反应。生长迟缓的癌症使用不同的策略来逃避免疫系统的破坏。肿瘤免疫学家对影响hla抗原表达和/或功能的免疫逃避机制特别感兴趣,因为这些分子在恶性细胞与免疫细胞的相互作用中起着至关重要的作用。本文综述了免疫控制点在免疫抑制中的潜在作用以及恢复免疫细胞毒性的治疗策略。
This review provides updated information on HLA class I and II antigens in cancer. The expression of HLA antigens in normal and tumor tissues, the physiological organization of the components of HLA antigen-processing machinery, the expression patterns of HLA antigens associated with the molecular and regulatory defects identified to date, as well as their functional and clinical significance, are described. This review summarizes clinical and experimental data on the complexity of immune escape mechanisms used by tumour cells to avoid T and natural killer cell responses. The variety of class I HLA phenotypes that can be produced by tumor cells during this process is presented. We also discuss here the potential capacity of metastatic lesions to recover MHC/HLA class I expression after immunotherapy, which depends on the reversible/ soft or irreversible/hard nature of the molecular mechanism responsible for the altered HLA class I phenotypes, and which determines the progression or regression of metastatic lesions in response to treatment. HLA сlass II genes play key roles in connecting innate and adaptive immunity in tumor rejection and when the escape route via HLA-I is already established. Antigens сlass II HLA expression in tumor cells and gives tumor cells the ability to present antigens, becoming less aggressive, and improves prognosis. Malignant tumors, as a genetic disease, are caused by structural alterations of the genome which can give rise to the expression of tumor-associated antigens in the form of either structurally altered molecules or of overexpressed normal molecules. Tumor associated antigens recognized by the immune system and induce a T-cell-mediated immune response. Outgrowing cancers use different strategies to evade destruction by the immune system. Immune evasion mechanisms affecting the expression and/or function of HLA-antigens are of special interest to tumor immunologists, since these molecules play a crucial role in the interaction of malignant cells with immune cells. This review describes the potential role of immunity control points in immunosuppression and therapeutic strategies for restoring the cytotoxicity of immune cells.