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. 2019 Jan 30;105(3):551–563. doi: 10.1002/JLB.4A0617-242RRR

Table 1.

Study population HLA allotypes and presence of KIR2DL1, KIR2DL2, KIR2DS2, KIR2DL3, and KIR3DL1 genes

Bw4/62 C1/C2 HLA‐A HLA‐B HLA‐C 2DL1 2DL2 2DS2 2DL3 3DL1
2 a Bw4b C1/C2c 02:01 24:02 44:02 51:01 05 08 +d + + + +
3 Bw4/6 C1/C2 02:01 31:01 27:01 40:01 03:02 15:02 + + +
5 e Bw4/6 C1/C2 02:01 02:01 08:01 44:02 01:01 04:01 + + +
6 f Bw4 C1/C2 31:01 68:01 27:08 51:01 02:02 12:03 + * +
12 e Bw4/6 C1/C1 01:01 23:01 14:01 38:05 08:02 12:03 + + +
21 f Bw4/6 C2/C2 02:01 02:01 07:02 57:01 05 06:02 + + +
23 Bw6 C1/C1 02:01 02:01 18:01 40:01 03:04 07:01 + + +
29 Bw6 C1/C1 02:01 02:01 07:02 08:01 07 07 + + + + +
30 f Bw6 C1/C2 02:01 30:02 07:02 35:01 04:01 07:02 + + +
31 Bw6 C1/C1 02:01 03:01 07:02 40:01 03:02 07:10 + + + + +
32 f Bw6 C1/C2 03:01 11:01 07:02 35:01 04:01 07:02 + + +
38 Bw6 C1/C2 02:01 33:03 15:01 35:08 03:03 04:01 + + + + +
34 Bw6 C1/C1 01:01 02:01 08:01 40:01 03:02 07:01 + + + + +
44 Bw4/6 C2/C2 01:01 02:01 15:01 57:01 05 06:02 + + + +
45 Bw4 C1/C2 01:01 02:01 38:01 57:01 06:02 12:03 + + +
48 Bw4/6 C1/C2 01:01 03:01 14:02 57:01 06:02 08:02 + + + + +
49 Bw4 C1/C2 01:01 26:01 38:01 57:01 06:02 12:03 + + +
50 Bw4 C2/C2 02:02 30:02 53:01 57:03 04:01 18 + + + + +
51 Bw4/6 C2/C2 01:01 68:02 18:01 57:01 05:01 06:02 + + + + +
52 e Bw6 C2/C2 02:01 02:01 35 40 04:01 04:01 + +
53 e Bw6 C1/C1 03:01 03:01 18:01 35 03:03 16:01 + +
54 e Bw4/6 C1/C1 02:01 24:02 39:01 51:01 07:02 07:02 + +
a

Subject codes from #2 through #50 are the same as those used in Table S1.

b

Bw4 = Bw4 homozygote, Bw6 = Bw6 homozygote with no Bw4 at the HLA‐A locus, Bw4/6 = carriers of a Bw4 and Bw6 allele.

c

C1/C1 = HLA‐C1 group homozygotes, C2/C2 = HLA‐C2 group homozygotes, C1/C2 = carriers of both a C1 and C2 group allotype.

d

“‐” = absent; “+” = present.

e

Subjects contributing PBMC used to isolate single positive inhibitory NK receptor positive (SPiNKR+) NK cells for use as effector cells for ADCC‐GranToxuLux (ADCC‐GTL) assays only.

f

Subjects contributing PBMC used in both antibody‐dependent NK cell activation assays and to isolate SPiNKR+ for use as effector cells for ADCC‐GTL assays.