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

PALMA, MARÍA BELÉN; TRONIK-LE ROUX, DIANA; AMÍN, GUADALUPE; CASTAÑEDA, SHEILA; MÖBBS, ALAN M.; SCARAFIA, MARÍA AGUSTINA; LA GRECA, ALEJANDRO; DAOUYA, MARINA; PORAS, ISABELLE; INDA, ANA MARÍA; MORO, LUCÍA N.; CAROSELLA, EDGARDO D.; GARCÍA, MARCELA N.; MIRIUKA, SANTIAGO G.

Scientific Reports

Nature Research

Año: 2021 vol. 11

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.