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Journal of Clinical Pathology 2004;57:101-103; doi:10.1136/jcp.57.1.101
Copyright © 2004 by the BMJ Publishing Group Ltd & Association of Clinical Pathologists.
Journal of Clinical Pathology 2004;57:101-103
© 2004 BMJ Publishing Group Ltd & Association of Clinical Pathologists

SHORT REPORT

Influence of recipient and donor IL-1{alpha}, IL-4, and TNF{alpha} genotypes on the incidence of acute renal allograft rejection

H Lee1, B Clark1, H C Gooi1, J Stoves2, C G Newstead2

1 Department of Transplantation Immunology, St James’s University Hospital, Leeds, LS9 7TF, UK
2 Renal Transplant Unit, St James’s University Hospital

Correspondence to:
Correspondence to:
Dr H Lee
Transplantation Laboratory, Manchester Royal Infirmary, Oxford Road, Manchester, M13 9WL, UK; helena.lee{at}cmmc.nhs.uk

ABSTRACT

Aims: To determine whether polymorphisms of the genes encoding donor or recipient interleukin 1{alpha} (IL-1{alpha}), tumour necrosis factor {alpha} (TNF{alpha}), or IL-4 have any impact on the incidence of acute rejection after renal transplantation.

Methods: All donors and recipients were genotyped for three polymorphisms in the three cytokine genes: IL1A -889, TNFA -308, and IL4 –590.

Results: Statistical analysis of the data obtained revealed no association between the cytokine gene polymorphisms tested and the incidence of post-transplant acute rejection. After stratification for human leucocyte antigen (HLA) matching, it was found that kidneys from donors positive for the TNFA-A allele had a significantly increased incidence of acute rejection in HLA-DR mismatched transplants.

Conclusions: This finding argues for prospective TNFA genotyping of renal donors, with avoidance of allocation of kidneys from donors positive for the TNFA-A allele to HLA-DR mismatched recipients.

Keywords: acute renal allograft rejection; donor cytokine genotype; recipient cytokine genotype

Abbreviations: IL, interleukin; HLA, human leucocyte antigen; MHC, major histocompatibility complex; PCR, polymerase chain reaction; TNF, tumour necrosis factor


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