Figure 1.
A CRISPR library screen identifies ATLL cell-intrinsic molecules for immune escape from YT1–NK cell line-mediated cytotoxicity. (A) Schematic design of CRISPR library screening in this study. Two Cas9-expressing ATLL cell lines, ST1 and KK1, were analyzed. (B) Selection criteria for ATLL cell-intrinsic genes whose knockout lead to escape from NK cytotoxicity. (C) Log2 fold changes (treated/not treated) of single guide RNAs (sgRNAs) targeting selected resistance genes. (D) Log2 fold changes (treated/not treated) of known NK-cell receptor ligands in our screening. (E) Selection criteria for ATLL-cell–intrinsic genes whose knockout lead to sensitization of NK cytotoxicity. (F) Log2 fold changes (treated/not treated) of sgRNAs targeting selected sensitizing genes.

A CRISPR library screen identifies ATLL cell-intrinsic molecules for immune escape from YT1–NK cell line-mediated cytotoxicity. (A) Schematic design of CRISPR library screening in this study. Two Cas9-expressing ATLL cell lines, ST1 and KK1, were analyzed. (B) Selection criteria for ATLL cell-intrinsic genes whose knockout lead to escape from NK cytotoxicity. (C) Log2 fold changes (treated/not treated) of single guide RNAs (sgRNAs) targeting selected resistance genes. (D) Log2 fold changes (treated/not treated) of known NK-cell receptor ligands in our screening. (E) Selection criteria for ATLL-cell–intrinsic genes whose knockout lead to sensitization of NK cytotoxicity. (F) Log2 fold changes (treated/not treated) of sgRNAs targeting selected sensitizing genes.

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