Title of article :
The recipient CXCL10 + 1642C>G variation predicts survival outcomes after HLA fully matched unrelated bone marrow transplantation
Author/Authors :
Nakata، نويسنده , , Katsuya and Takami، نويسنده , , Akiyoshi and Espinoza، نويسنده , , J. Luis and Matsuo، نويسنده , , Keitaro and Morishima، نويسنده , , Yasuo and Onizuka، نويسنده , , Makoto and Fukuda، نويسنده , , Takahiro and Kodera، نويسنده , , Yoshihisa and Akiyama، نويسنده , , Hideki and Miyamura، نويسنده , , Koichi and Mori، نويسنده , , Takehiko and Nakao، نويسنده , , Shinji، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2013
Pages :
8
From page :
104
To page :
111
Abstract :
CXCL10 is a chemoattractant for immune cells that is involved in several immune-inflammatory disorders. This study retrospectively examined the impact of a single nucleotide variation (rs3921, + 1642C>G) in the CXCL10 gene on transplant outcomes in a cohort of 652 patients who underwent unrelated HLA-matched bone marrow transplantation (BMT) for hematologic malignancies. The recipient C/G or G/G genotype was found to be associated with a significantly better 5-year overall survival (OS) rate and a lower transplant-related mortality (TRM) rate than the recipient C/C genotype. The recipient C/G or G/G genotype also predicted a reduced incidence of death due to organ failure. The multivariate analysis showed the recipient C/G or G/G genotype to exhibit statistical trends toward beneficial effects on OS but not on TRM. CXCL10 genotyping could therefore be useful in predicting prognoses and creating therapeutic strategies for improving the final outcomes of patients who undergo allogeneic BMT.
Keywords :
Chemokine , Bone marrow transplantation , CXCL10 , Single nucleotide variation , Organ failure , unrelated donor
Journal title :
Clinical Immunology
Serial Year :
2013
Journal title :
Clinical Immunology
Record number :
1856094
Link To Document :
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