Table 1a.
Example of how a patient typing is evaluated.
| Patient typing: A*02:05, 68:04; B*35:DNXN, 53:01; DRB1*03:01, 13:03; C*04:01; DQB1*02:01, 02:02 | ||
|---|---|---|
| Issue noted | Web site providing information | Action/Resolution |
| Is information included on all the loci required for matching? | If the transplant center would like to search for a 10/10 match, assignments must be included for 5 loci; for a 8/8 match, 4 loci. The typing includes all the required loci for either level of match. | |
| Evaluate resolution of testing: Allele B*35:DNXN has an allele code |
http://Bioinformatics.nmdp.org DNA Type Lookup Tool | Expand to full allele string. Depending on the assignments, request additional typing to increase the resolution. In this case, the assignment includes only alleles that share the sequence of exons 2 and 3: B*35:01, B35:40N, B35:42, B35:57, B35:94. |
| Evaluate resolution of testing: C*04:01 allele is at high resolution but this level of resolution required special testing by the HLA laboratory |
http://hla.alleles.org/alleles/index.html G groups | Ask the laboratory if it specifically excluded the other alleles that carry the same nucleotide sequence as C*04:01 in the HLA-C exons specifying the peptide binding site. For example, did the laboratory specifically exclude the non- expressed allele C*04:09N? (see Note 46) |
| Evaluate frequency of alleles: Allele A*68:04 is uncommon |
http://Bioinformatics.nmdp.org Rare Allele List | In family? If yes, acceptable. If no, repeat HLA typing of HLA-A preferably with different reagents/method. |
| Investigate B/C and DR/DQ haplotypes: B *35:DNXN with C *04:01 B*53:01 with C*04:01 DRB1*03:01 with DQB1*02:01 or *02:02 DRB1*13:03 with DQB1*02:01 or *02:02 |
http://www.haplostats.org/home.do | Concordant with family typing? Common or uncommon? In this case, the B-C associations are common. Both DRB1 alleles are frequently observed with DQB1*02:01 but not with DQB1*02:02 so this is unusual. The laboratory should be asked to confirm the DQB1*02:02 assignment if it is not observed in the family. |
| Investigate multi-locus haplotypes (A/B/C/DRB1/DQB1) | http://www.haplostats.org/home.do | Concordant with family typing? Common or uncommon? |