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. 2015 Oct 29;5(4):e1093721. doi: 10.1080/2162402X.2015.1093721

Table 4.

Diversity of iKIR2D/HLA-C licensing interactions in controls and myeloma patients.

  Frequency, n (%)
Multivariate logistic regression
Combinations of conventional iKIR2D/HLA-C licensing interactions1 Controls (n=286 ) SMM+MM (n=78 ) OR Analysis 95%CI p
No iKIR2D/HLA-C interactions2 1 (0.35%) 2 (2.56%) 15.014 1.171–195.55 0.037
Single-KIR2DL3+/C1+ 31 (10.84%) 16 (20.51%) 2.795 1.183–6.603 0.019
Single-KIR2DL2+/C1+ 14 (4.9%) 10 (12.82%) 5.182 1.795–14.960 0.002
Single-KIR2DL1+/C2+ 53 (18.5%) 9 (11.54%) 1.089 0.426–2.728 0.858
Double-KIR2DL2+L3+/C1+ 51 (17.83%) 6 (7.69%) 0.727 0.255–2.068 0.550
Double-KIR2DL1+L3+/C2+C1+ 53 (18.53%) 18 (23.08%) 1.936 0.855–4.382 0.113
Double-KIR2DL1+L2+/C2+C1+ 13 (4.56%) 5 (6.41%) 2.335 0.703–7.758 0.166
Triple-KIR2DL1+L2+L3+/C2+C1+3 70 (24.48%) 12 (15.38%) 1.0 N.A. 0.004

OR, odd ratio; 95%CI, 95% confidence interval.

1

Ordered following previously described (conventional) KIR2D-ligand affinity hierarchy: KIR2DL3/C1 < KIR2DL2/C1 < KIR2DL1/C2.37

2

Patients with no conventional iKIR2D/HLA-C licensing interactions (but with the non-conventional KIR2DL2/C2 interaction).

3

Reference category. N.A.: no applicable.