CC chemokine receptor 5 and renal-transplant survival

Background About 1% of white populations are homozygous carriers of an alle le of the gene for the CC chemokine receptor 5 (CCR5) with a 32 bp deletion (CCR5 Delta 32), which leads to an inactive receptor. During acute and chr onic transplant rejection, ligands for CCR5 are upregulated, and the graft is infiltrated by CCR5-positive mononuclear cells. We therefore investigate d the influence of CCR5 Delta 32 on renal-transplant survival Methods Genomic DNA from peripheral-blood leucocytes of 1227 renal-transpla nt recipients was screened by PCR for the presence of CCR5 Delta 32. Demogr aphic and clinical data were extracted from hospital records. Complete foll ow-up data were available for 576 recipients of first renal transplants. Gr aft survival was analysed by Fisher's exact test and Kaplan-Meier plots com pared with a log-rank test. Findings PCR identified 21 patients homozygous for CCR5 Delta 32 (frequency 1.7%). One patient died with a functioning graft. Only one of the remainin g patients lost transplant function during follow-up (median 7.2 years) com pared with 78 of the 555 patients with a homozygous wild-type or heterozygo us CCR5 Delta 32 genotype. Graft survival was significantly longer in the h omozygous CCR5 Delta 32 group than in the control group (log-rank p=0.033; hazard ratio 0.367 [95% CI 0.157-0.859]). Interpretation Patients homozygous for CCR5 Delta 32; show longer survival of renal transplants than those with: other genotypes, suggesting a pathoph ysiological role for CCR5 in transplant Loss. This receptor may be a useful target for the prevention of transplant loss.