4.7 Article

HLA-G gene editing in tumor cell lines as a novel alternative in cancer immunotherapy

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SCIENTIFIC REPORTS
卷 11, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41598-021-01572-0

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  1. Scientific and Technical Research Fund (FONCyT) [PICT-2015-1469] Funding Source: Medline
  2. Consejo Nacional de Investigaciones Científicas y Técnicas [PIP 112-20150100723] Funding Source: Medline

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The study successfully achieved downregulation of HLA-G expression in tumor cells using CRISPR/Cas9 gene editing, leading to enhanced in vitro immune cell response. This finding provides an important foundation for the development of novel clinical immunotherapeutic approaches in cancer.
Cancer immunotherapies based mainly on the blockade of immune-checkpoint (IC) molecules by anti-IC antibodies offer new alternatives for treatment in oncological diseases. However, a considerable proportion of patients remain unresponsive to them. Hence, the development of novel clinical immunotherapeutic approaches and/or targets are crucial.W In this context, targeting the immune-checkpoint HLA-G/ILT2/ILT4 has caused great interest since it is abnormally expressed in several malignancies generating a tolerogenic microenvironment. Here, we used CRISPR/Cas9 gene editing to block the HLA-G expression in two tumor cell lines expressing HLA-G, including a renal cell carcinoma (RCC7) and a choriocarcinoma (JEG-3). Different sgRNA/Cas9 plasmids targeting HLA-G exon 1 and 2 were transfected in both cell lines. Downregulation of HLA-G was reached to different degrees, including complete silencing. Most importantly, HLA-G - cells triggered a higher in vitro response of immune cells with respect to HLA-G + wild type cells. Altogether, we demonstrated for the first time the HLA-G downregulation through gene editing. We propose this approach as a first step to develop novel clinical immunotherapeutic approaches in cancer.

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