Thymic function, anti-thymocytes globulins, and cancer after renal transplantation.

Date publication

juillet 2011

Auteurs

Membres identifiés du Cancéropôle Est :
Pr BORG Christophe , Pr CHALOPIN Jean-Marc , Pr DUCLOUX Didier , Dr FERRAND Christophe

Tous les auteurs :
Ducloux D, Bamoulid J, Courivaud C, Gaugler B, Rebibou JM, Ferrand C, Chalopin JM, Borg C, Tiberghien P, Saas P

Lien Pubmed

https://www.ncbi.nlm.nih.gov/pubmed/21620972

Résumé

BACKGROUND: Prolonged CD4 T cell lymphopenia after polyclonal antithymocyte globulins (ATG) is associated with an increased rate of cancers. Here, we examined whether pre-transplant thymic function estimated by TREC levels is predictive of cancer occurrence following ATG treatment. PATIENTS AND METHODS: The impact of TREC on cancer occurrence was analyzed in 115 consecutive incident renal transplant recipients having received ATG. RESULTS: Mean follow-up was 7.5+/-2.6years. After ATG induction, patients with the lowest pre-transplant TREC values had lower post-transplant CD4(+) and CD4(+) CD45RA(+) CD45RO(-) T cell counts, and a higher frequency of T cells with a regulatory phenotype (CD127(+)CD4(+)CD25(+)Foxp3(+)). Log-transformed pre-transplant TREC values were significantly lower in patients who developed cancer after transplantation (p

Référence

Transpl Immunol. 2011 Jul;25(1):56-60