Zusammenhang der Interleukin-6-Polymorphismen 174 und 597 bei Empfänger und Spender mit dem Therapieergebnis nach allogener hämatopoetischer Stammzelltransplantation im Kindesalter

The success of allogeneic hematopoietic stem cell transplantation (HSCT) is compromised by complications such as infection, relapse, and graft-versus-host disease (GVHD). The investigation of non-HLA immunogenetics could identify predictors of an unfavorable outcome after allogeneic HSCT. We examined the impact of single nucleotide polymorphisms (SNPs) within the promoter region of interleukin 6 (IL6) on the development of GVHD after pediatric allogeneic HSCT. In this retrospective analysis, we included 320 pediatric patients with a median age of 10 years who underwent an allogeneic HSCT and their respective donors. The IL6-174 polymorphism was examined in 300 recipients and 295 donors. We investigated the infuence of the IL6-174 and IL6-597 polymorphisms on overall survival, event-free survival, relapse incidence, transplant-related mortality, and the occurrence of GVHD. G polymorphism at position 174 of the recipient IL6 gene was associated with a higher incidence of acute GVHD. Patients with IL6-597 GG genotype developed acute GVHD more frequently than individuals with an A allele. IL6-174 GG homozygous recipients had a more frequent occurrence of chronic GVHD. We observed a signifcant increased risk of chronic GVHD in recipients with IL6-597 GG genotype. Polymorphisms of donors did not affect the incidence of acute GVHD and chronic GVHD. In multivariate analysis, the IL6-174 and IL6-597 SNPs were independent signifcant risk factors for acute GVHD as well as for chronic GVHD. In addition, older age at time of transplantation turned out to be a signifcant risk factor for chronic GVHD. Our study identifed the IL6-174 and IL6-597 GG genotypes of pediatric allogeneic HSCT recipients as genetic risk factors for the development of acute GVHD and chronic GVHD. After evaluations in further studies, these fndings could implicate the adjustment of prophylactic measures to reduce the occurrence of acute GVHD and chronic GVHD.

Cite

Citation style:
Could not load citation form.

Rights

Use and reproduction: