CLINICAL IMPORTANCE OF PRE-MORTEUM BLOOD-LYMPHOCYTES IN CADAVER DONORTISSUE TYPING

Citation
S. Vaidya et al., CLINICAL IMPORTANCE OF PRE-MORTEUM BLOOD-LYMPHOCYTES IN CADAVER DONORTISSUE TYPING, Clinical transplantation, 9(3), 1995, pp. 165-170
Citations number
NO
Categorie Soggetti
Surgery,Transplantation
Journal title
ISSN journal
09020063
Volume
9
Issue
3
Year of publication
1995
Part
1
Pages
165 - 170
Database
ISI
SICI code
0902-0063(1995)9:3<165:CIOPBI>2.0.ZU;2-R
Abstract
We have refined our immunomagnetic bead (IM bead) procedures to isolat e pure and viable lymphocyte subpopulation from premorteum (PM) blood for cadaver donor HLA typing, preliminary and final crossmatches (XMs) . The results of 1220 XMs were compared using T/B lymphocytes isolated either from PM blood or spleen/lymphnode (SPLN) tissue. IM bead techn ique was used to isolate T/B cells from PM blood and nylon wool column (NWC) techique was used to isolate T/B cells from SPLN. When we compa red the outcome of 800 T-cell crossmatches using T cells from PM blood or SPLN of 5 separate cadaver donors, NWC TXMs tended to be more fals enegative for high PRA (>10%, total 500 XMs), as well as low PRA (<10% , total 300 XMs) did not reach statistical significance. In contrast, NW BXM (420 B XM) were found to be far more false negative than IM bea d BXM regardless of the PRA of the patients. In order to ensure that N WC BXMs were indeed false negative, 23 sera with known anti-DR antibod ies were BXMed where antigen-specific B cells were isolated by both th e techniques. Our results showed that IM bead BXM identified the DR sp ecificities greater than 90% of the time, the titers of ab specificiti es were stronger (1:8). In comparison, NWB cell XMs were weak (titers 1:2), and the false negative rate for some ab was as high as 73%. Usin g IM bead and NWC techniques we compared our turnaround time (TAT) for cadaver donor typing, preliminary and final XMs. Using PM blood with IM bead, our TAT was less than 5 hours for the entire cadaver donor wo rk-up. In contrast, TAT from SPLN with NWC technique was as long as 8 hours. We also compared graft survival statistics of 153 patients tran splanted on a basis of negative T/BXM using either PM blood lymphocyte s (98 patients) or SPLN lymphocytes (55 patients). However, lymphocyte s in either case were isolated by IM bead assay We found no adverse ou tcome due to usage of PM blood lymphocytes in terms of long- or short- term graft survival or incidence of hyperacute rejection. In fact, col d ischemia time (CIT) was much shorter (median 12 hours) in the PM gro up versus more than 20 hours in SPLN group. In summary, PM blood is an ideal source of T/B lymphocytes for the solid organ pretransplant wor kup and final XM.