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Katrine Keilsen and colleagues of Copenhagen University Hospital Rigshospitalet in Denmark conducted a study correlating risk of adverse post-transplant outcomes with interleukin-7 (IL-7) polymorphisms. The findings were published in the February 2018 issue of Frontiers in Immunology.
IL-7 is integral for T-cell development in the thymus and peripheral T-cell homeostasis. The IL-7 receptor consists of a CD132 chain and an IL-7 receptor alpha chain (IL-7 Rα). Studies of the single nucleotide polymorphisms (SNPs) of IL-7 Rα have shown association with increased incidence of autoimmune inflammatory diseases and impact on timing of immune recovery in HIV patients. The aim of this study was to analyze transplant outcomes based on donor genotype of the rs6897932 SNP of IL-7 in allogeneic stem cell transplant patients.
This study reviewed the correlation of transplant related outcomes to donor IL-7 genotypes. In general, patients who were homozygous or heterozygous for the T allele, had adverse results in several outcome measures, compared to those homozygous for the C allele. Heterozygosity of the T allele lead to an increase in aGVHD and TRM, in addition to decreased OS. Heterozygous TT donor products lead to an increase in cGVHD and CMV infections. This data is useful for consideration of donor genotype testing pre-transplant, to help improve patient outcomes.
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