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. 2022 Feb 22;13:845474. doi: 10.3389/fgene.2022.845474

TABLE 3.

Frequency of KIR and HLA class I ligand combination in the control group and COVID-19 patients.

Hospitalized COVID-19 patients
All patients (A) n = 200 Mild (M) n = 93 Severe (S) n = 107 Controls (C) n = 195 Comparisons: p-value, OR (95% CI)
Inhibitory KIR + HLA class I ligand %F (N+) %F (N+) %F (N+) %F (N+)
 2DL1+C2+ 55.5 (111) 62.4 (58) 49.5 (53) 55.4 (108)
 2DL2+C1+ 42.5 (85) 43.0 (40) 42.1 (45) 37.9 (74)
 2DL3+C1+ 80.0 (160) 79.6 (74) 80.4 (86) 72.3 (141)
 3DL1+Bw4+ 44.5 (89) 45.2 (42) 43.9 (47) 55.4 (108) AxC: 0.03, 0.65 (0.43–0.96)
 3DL1+Bw4 I80+ 32.5 (65) 34.4 (32) 30.8 (33) 32.8 (64)
 3DL1+Bw4 T80+ 18.5 (37) 15.1 (14) 21.5 (23) 27.7 (54) AxC: 0.03, 0.6 (0.37–1.0); MxC: 0.02, 0.46 (0.24–0.9)
 3DL2+A3/A11+ 25.0 (50) 26.9 (25) 23.4 (25) 35.4 (69) AxC: 0.02, 0.6 (0.4–0.94); SxC: 0.03, 0.56 (0.3–0.95)
 3DL2+A3+ 11.5 (23) 15.1 (14) 8.4 (9) 26.1 (51) AxC: 0.0003, 0.37 (0.21–0.63); MxC: 0.037, 0.5 (0.26–0.96); SxC: 0.0004, 0.26 (0.1–0.6)
 3DL2+A11+ 15.0 (30) 12.9 (12) 16.8 (18) 11.3 (22)
 3DL1+Bw4+ and 3DL2+A3/A11+ 9.5 (19) 10.8 (10) 8.4 (9) 15.4 (30)
 3DL1+Bw4+ and/or 3DL2+A3/A11+ 60.0 (120) 61.3 (57) 58.9 (63) 75.4 (147) AxC: 0.001, 0.49 (0.32–0.75); MxC: 0.015, 0.52 (0.3–0.9); SxC: 0.003, 0.5 (0.28–0.77)
 (3DL1+ Bw4+)- or (3DL2+A3/A11+)- 50.5 (101) 50.5 (47) 50.5 (54) 60.0 (117)
 (3DL1+Bw4+)- and (3DL2+A3/A11+)- 40.0 (80) 38.7 (36) 41.1 (44) 24.6 (48) AxC: 0.001, 2.04 (1.33–3.14); MxC: 0.015, 1.93 (1.1–3.3); SxC: 0.003, 2.14 (1.3–3.5)
Activating KIR + HLA class I ligand
 3DS1+Bw4+ 19.5 (39) 18.3 (17) 20.6 (22) 21.5 (42)
 2DS1+C2+ 25.5 (51) 24.7 (23) 26.2 (28) 22.5 (44)
 2DS2+C1+ 45.0 (90) 45.2 (42) 44.9 (48) 37.9 (74)
 2DS2+A11+ 7.5 (15) 5.4 (5) 9.3 (10) 4.6 (9)
 2DS5+C2+ 23.5 (47) 21.5 (20) 25.2 (27) 22.1 (43)
Inhibitory KIR + HLA class I ligand + Activating KIR
 3DL1+Bw4+ and 3DS1- 28.5 (57) 28.0 (26) 29.0 (31) 36.9 (72)
 3DL1+Bw4+ and 3DS1+ 16.0 (32) 17.2 (16) 15.0 (16) 18.5 (36)
 2DL1+C2+ and 2DS1- 32.0 (64) 39.8 (37) 25.2 (27) 34.9 (68) SxM: 0.03, 0.51 (0.23–0.93)
 2DL1+C2+ and 2DS1+ 23.5 (47) 22.6 (21) 24.3 (26) 21.0 (41)
 2DL1+C2+ and 2DS5- 34.0 (68) 41.9 (39) 27.1 (29) 34.9 (68) SxM: 0.03, 0.51 (0.28–0.93)
 2DL1+C2+ and 2DS5+ 21.5 (43) 20.4 (19) 22.4 (24) 20.5 (40)
 2DL1+C2+ and 2DS1-2DS5- 29.5 (59) 36.6 (34) 23.4 (25) 31.3 (61) SxM: 0.04, 0.53 (0.29–0.98)
 2DL1+C2+ and 2DS1+2DS5+ 19.0 (38) 17.2 (16) 20.6 (22) 17.4 (34)

Frequency (%F) of each genotype is expressed as a percentage and defined as the number of individuals having the genotype (N+) divided by the number of individuals studied (n) in the study group;OR, Odds ratio; CI, Confidence interval; Comparisons: AxC, all patients vs. controls, MxC, mild vs. controls, SxC, severe vs. controls, SxM, sever vs. mild.

Values shows significant difference are shown in bold.