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. 2021 Aug 4;11:15782. doi: 10.1038/s41598-021-95245-7

Figure 5.

Figure 5

KIR2DL3 inhibits conventional T lymphocyte response against target cells expressing C1 ligands and HLA-C*04 C2 ligand with higher effect on allogeneic than autologous ligands. (A) KIR2DL3+ and KIR2DL3 HLA-A2-pp65 specific T cell degranulation observed after 5 h incubation in the presence of pp65 (0, 0.01, and 0.1 µg/ml) loaded autologous EBV-B cell line, (B) allogeneic C1C1 ChT (HLA-C*03:04) and HiD (HLA-C*03:04; C*08:01) EBV-B cell lines, (C) C2C2 JVM (HLA-C*05:01) and BM9 (HLA-C*04:01) EBV-B cell lines at an effector: target ratio of 10:1 for three representative individuals (C1C1 I6, C1C2 I10 and C2C2 I19). Experiments were performed from 5 C1C1, 3 C1C2 and 2 C2C2 blood donors. (D) Violin plots of KIR2DL3+ and KIR2DL3 HLA-A2-pp65 specific T cell degranulation observed after 5 h incubation in the presence of pp65 (0.1 µg/ml) loaded C1C1 EBV-B cell lines for 5 C1C1, 3 C1C2 and 2 C2C2 blood donors. Paired t test was used to evaluate whether values between KIR2DL3+ and KIR2DL3 T cell degranulation were significantly different. **, *** and ****indicate p < 0.01, p < 0.001 and p < 0.0001 respectively. (E) KIR2DL3+ and KIR2DL3 HLA-A2-pp65 specific T cell degranulation observed after 5 h incubation in the presence of pp65 (0, 0.01, and 0.1 µg/ml) loaded allogeneic C1C1 and C2C2 immature dendritic cells at an effector: target ratio of 10:1 for one representative C1C1 (I6) and (F) C2C2 individuals (I19). (G) KIR2DL2+ HLA-A2-pp65 specific T cell degranulation observed after 5 h incubation in the presence of pp65 (0, 0.01, and 0.1 µg/ml) loaded allogeneic C1C1 (ChT, HiD) and C2C2 (JVM, BM9) EBV-B cell lines for one representative C1C1 individual (I4).