Patients were tested for class I HLA Ab by CDC-AHG (Lambda Cell Tray™), SAB (LABScreen® Single Antigen), and C1q-AHG (C1qScreen™ + wash and AHG); sera were EDTA treated prior to SAB/C1q testing. Sera were also tested by SAB at 1/8 dilution (n = 6) .36 samples were tested from 35 patients.
CDC results were 0% PRA (n = 6), 17–74% (n = 15), and >80% (n = 15). If Ab specificity could be assigned by CDC, these Ab were detected by SAB and C1q but additional specificities were present including in 2 of the patients with CDC 0% PRA. Also, 2 sera had Ab missed by CDC due to difficult tail analysis. There is no clear SAB MFI threshold where Ab is detected by CDC. MFI values of 8000–10,000 consistently result in a CDC positive result although lower values may also do so. Similar Ab were detected by SAB and C1q but there is often a lack of agreement between most reactive beads. The diluted sera suggest better agreement with C1q results; dilution may detect Ab NOT detected by SAB testing as shown in Patient 1. Patient 2 shows no prozone.
It is hard to compare SAB and CDC as cells are phenotypic, readout is subjective, and Ab specificity can’t be assigned if PRA is high. The few diluted samples tested appear to be comparable to C1q but further dilution studies are ongoing. Dilution testing involves less change to current practice of SAB testing and fits easily in work flow, enabling faster TAT. These results represent SAB and C1q-AHG testing in platelet refractory patients, but may be extended to solid organ transplant to investigate the strength of Ab. Platelet transfusion outcomes are available for 10 patients but relevance review is ongoing.