Table 5.
Pros and cons of scoring strategies for NK alloreactivity assessment.
| Models | NK cells of the donor alloreactive toward host cells when: | Pros | Cons |
|---|---|---|---|
| Ligand–ligand model | Recipient is lacking an MHC class I ligand that is present in the donor | No KIR typing requiredEasy to use (online algorithm) | Simple approximation of educational modelApproximate estimation of the mismatches if using the IPD database (does not take into account HLA-Bw4 epitopes related to HLA-A and HLA-C or HLA-A3/11 epitopes) |
| Receptor–ligand model | At least one KIR gene expressed in the donor does not recognize any of the MHC molecules of the recipient | KIR typing only at genic resolution for donors | |
| Educational models | Donor has educated NK cells—i.e., KIR and its cognate MHC ligand—but the recipient lacks the cognate KIR MHC ligand | KIR typing only at genic resolution for donorsMost comprehensive model for NK alloreactivity | Delicate process that can be overridden in certain conditions, e.g., high inflammation surroundings such as in aHSCT |
| Haplotypes | Donor has at least one KIR B haplotype | KIR typing only at genic resolution for donorsEasy to use (online algorithm) | |
| Gene–gene model | KIR gene is present in the donor but absent in the recipient | Easy to use | Far from any biological underlying process |
| Allelic polymorphisms | A specific D/R interaction is present | Directly targets a functional gene difference | Multitude of models with variable relevance |
| Allelic KIR genotyping (time and cost) | |||
| Complex |