Xinmeng Guo, Jinning Zhang, Jin Shang, Yanfei Cheng, Shuang Tian, Yuanqing Yao
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引用次数: 0
摘要
威胁妇女健康的妇科肿瘤,特别是晚期和复发的妇科肿瘤,目前的治疗方法大多难以治愈。因此,迫切需要新的治疗靶点。人白细胞抗原- g (HLA-G)是一种非经典的主要组织相容性复合体I类分子,通常在胎儿中表达,以保护胎儿免受母体免疫系统的破坏。HLA-G也在病理条件下表达,如在实体肿瘤中,并可能参与肿瘤的发展,并作为癌症中新的免疫检查点。此外,它在大多数妇科肿瘤中表达。因此,抑制HLA-G及其受体阻断免疫逃逸途径可能是癌症免疫治疗的新策略。据我们所知,这篇综述首次总结了HLA-G在妇科肿瘤中的最新研究成果。我们强调的事实,HLA-G在妇科肿瘤组织中表达,其中它灭活免疫效应参与肿瘤进展。需要进一步研究HLA-G在妇科肿瘤中的作用,以便将HLA-G纳入恶性妇科疾病免疫治疗的设计和评估中。
Human leukocyte antigen-G in gynaecological tumours
Gynaecological tumours that threaten the health of women, especially when advanced and recurrent, have remained mostly intractable to existing treatments. Therefore, new therapeutic targets are urgently needed. Human leukocyte antigen-G (HLA-G) is a nonclassical major histocompatibility complex class I molecule typically expressed in foetuses for protection against destruction by the maternal immune system. HLA-G is also expressed under pathological conditions, such as in solid tumours, and may participate in tumour development and serve as a novel immune checkpoint in cancer. Furthermore, it is expressed in most gynaecological tumours. Therefore, inhibiting HLA-G and its receptors to block the immune escape pathway could represent a new strategy in cancer immunotherapy. To the best of our knowledge, this review is the first to summarize recent research findings on HLA-G in gynaecological oncology. We highlight the fact that HLA-G is expressed in gynaecological tumour tissues, wherein it inactivates immune effectors involved in tumour progression. Further studies on HLA-G in gynaecological oncology are needed to incorporate HLA-G into the design and evaluation of immunotherapy for malignant gynaecological diseases.
期刊介绍:
The International Journal of Immunogenetics (formerly European Journal of Immunogenetics) publishes original contributions on the genetic control of components of the immune system and their interactions in both humans and experimental animals. The term ''genetic'' is taken in its broadest sense to include studies at the evolutionary, molecular, chromosomal functional and population levels in both health and disease. Examples are:
-studies of blood groups and other surface antigens-
cell interactions and immune response-
receptors, antibodies, complement components and cytokines-
polymorphism-
evolution of the organisation, control and function of immune system components-
anthropology and disease associations-
the genetics of immune-related disease: allergy, autoimmunity, immunodeficiency and other immune pathologies-
All papers are seen by at least two independent referees and only papers of the highest quality are accepted.