A DTT- AMELIORATED POSITIVE
CROSSMATCH DOES NOT INFLUENCE RENAL GRAFT OUTCOME. C.F. Bryan, J. Martinez, N. Muruve, P.W.
Nelson, G.E. Pierce, G. Ross, C.F. Shield, B.A. Warady, M.I. Aeder, T.S.
Helling, A.M. Luger. Midwest Organ Bank, Inc., Westwood, KS.
A positive crossmatch that is rendered negative
by treating the serum with the IgM-reducing agent dithiotreitol (DTT) is
generally reported not to influence short-term renal graft outcome. Its
effect on long-term (³ 3 years) function,
however, is less clear. We evaluated the effect of a DTT-ameliorated positive
crossmatch (DTT-APXM) on long-term renal graft outcome in 1,025 consecutive
cadaveric renal transplants and 294 living-donor renal transplants from
patients transplanted between 1990 and 1997. Graft survival data for the
cadaveric transplants are in the following table.
DTT-AmelioratedPositive Crossmatch
Graft Survival (Years)
0.25
1
3
5
NO
94%
91%
85%
78%
(n=974)
(n=857)
(n=720)
(n=443)
(n=228)
YES
91%
87%
79%
70%
(n=51)
(n=44)
(n=39)
(n=24)
(n=10)
The data show that short-term and long-term
graft survival of cadaveric kidney transplants in patients with a DTT-APXM
is not significantly different from patients who had a negative untreated
crossmatch (Wilcoxon=0.2; log-rank=0.3). Similarly, no significant effect
was seen with living-donor renal transplants with the DTT-APXM group (n=4)
having 1-, 3- and 5-year survival of 100%, 100% and 75%, compared with
the negative crossmatch group (n=290) having 94%, 87% and 83% 1-, 3- and
5-year survival (Wilcoxon=0.7; log-rank=0.8).
Conclusion: The data show that long-term graft survival
in renal transplantation is not influenced by the presence of donor-reactive
lymphocytotoxic antibodies in the crossmatch if no reactivity is present
after the serum is treated with DTT.