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. 2016 Dec 14;150(3):248–264. doi: 10.1111/imm.12684

Table 2.

Specificities and reported cross‐reaction of killer‐cell immunoglobulin‐like receptors (KIR) antibodies

Clone Specificity Reported cross‐reaction and (comments) Reference
143211 KIR2DL1 KIR2DS5  192
HP‐3E4 KIR2DL1 KIR2DS1 and KIR2DS4 193
EB6 KIR2DL1, KIR2DS1 KIR2DL3*005  187, 194, 195
11PB6 KIR2DL1, KIR2DS1 KIR2DL3*005  194
HP‐MA4 KIR2DL1, KIR2DS1 KIR2DS3 and KIR2DS5  192, 193
GL183 KIR2DL2, KIR2DL3, KIR2DS2 196, 197, 198
DX27 KIR2DL2, KIR2DL3, KIR2DS2 52
CH‐L KIR2DL2, KIR2DL3, KIR2DS2 199
180701 KIR2DL3 (Does not recognize KIR2DL3*005 and *015) 187
ECM41 KIR2DL3 (Does not recognize KIR2DL3*005 and *015)  194
UP‐R1 KIR2DL5 200
1F12 KIR2DS2, KIR2DL3 201
179315 KIR2DS4 140
JJC11·6 KIR2DS4 KIR2DS3  192
FES172 KIR2DS4 202
DX9 KIR3DL1 203
5·133 KIR3DL1, KIR3DL2 All KIRs except KIR2DS1 and KIR2DS3 192
Z27 KIR3DL1, KIR3DS1 204, 205, 206
DX30 KIR3DL1/KIR3DL2 207
DX31 KIR3DL2 207
NKVFS1 PanKIR2D 208

Sequence homogeneity between KIR genes at the genomic level translates to high similarity between encoded protein products. As such, analysis of KIR expression is not trivial in primary cells because of the cross‐reaction of available antibodies, in particular between activating and inhibitory isoforms. This can lead to misinterpretation of cell‐staining results. These cross‐reactions must be taken into account when analysing KIR expression. Staining experiments can be supported with control stains, references, representative stains on relevant donors and precise descriptions of strategies for differential staining using sets of antibodies.