HLA-class-I expression loss, tumor microenvironment and breast cancer prognosis

IF 3.7 4区 医学 Q2 CELL BIOLOGY
Alexandra Giatromanolaki , Georgios D. Michos , Erasmia Xanthopoulou , Michael I. Koukourakis
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Abstract

Loss of HLA-class-I molecule expression by cancer cells is a frequent event in human tumors that may lead to immune evasion from cytotoxic T-cells. We examined the expression patterns of HLA-class-I molecules in a series of 175 patients with operable breast cancer (BCa). Extensive loss of BCa cell HLA-class-I expression was noted 76.6 % of patients (27.5 % complete loss). A significant association of HLA-preservation with high TIL-density (p = 0.001) was documented. Preservation of HLA was evident only in BCa carcinomas with low HIF1α expression and high TIL-density. Cell line experiments (MCF7 and T47D) showed that induction of HLAs in cancer cells following incubation with lymphocytes or IFNγ, was abrogated under hypoxic conditions. HLA-preservation was linked with better distant metastasis-free survival (p = 0.01), which was confirmed also in multivariate analysis (p = 0.02, HR 3.17). Studying the expression of HLA-class-I molecules in parallel with TIL-density and HIF1α expression may identify subgroups of BCa patients who would benefit from immunotherapy.

HLA-I 类表达缺失、肿瘤微环境与乳腺癌预后
癌细胞丧失 HLA-I 类分子表达是人类肿瘤中的常见现象,可能会导致细胞毒性细胞的免疫逃避。我们研究了一系列 175 名可手术乳腺癌(BCa)患者的 HLA-I 类分子表达模式。76.6%的患者(27.5%完全丧失)的BCa细胞HLA-class-I表达广泛丧失。HLA的保留与高TIL密度(p = 0.001)有明显关联。只有在低 HIF1α 表达和高 TIL 密度的 BCa 癌中,HLA 的保留才是明显的。细胞系实验(MCF7 和 T47D)表明,与淋巴细胞或 IFNγ 一起孵育后,癌细胞中的 HLAs 诱导在缺氧条件下会减弱。HLA 的保留与较好的无远处转移生存率有关(p = 0.01),这在多变量分析中也得到了证实(p = 0.02,HR 3.17)。将HLA-I类分子的表达与TIL密度和HIF1α的表达同时进行研究,可确定哪些BCa患者亚群可从免疫疗法中获益。
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来源期刊
Cellular immunology
Cellular immunology 生物-免疫学
CiteScore
8.20
自引率
2.30%
发文量
102
审稿时长
30 days
期刊介绍: Cellular Immunology publishes original investigations concerned with the immunological activities of cells in experimental or clinical situations. The scope of the journal encompasses the broad area of in vitro and in vivo studies of cellular immune responses. Purely clinical descriptive studies are not considered. Research Areas include: • Antigen receptor sites • Autoimmunity • Delayed-type hypersensitivity or cellular immunity • Immunologic deficiency states and their reconstitution • Immunologic surveillance and tumor immunity • Immunomodulation • Immunotherapy • Lymphokines and cytokines • Nonantibody immunity • Parasite immunology • Resistance to intracellular microbial and viral infection • Thymus and lymphocyte immunobiology • Transplantation immunology • Tumor immunity.
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