Oncotarget

Research Papers:

Associations between HVEM/LIGHT/BTLA/CD160 polymorphisms and the occurrence of antibody-mediate rejection in renal transplant recipients

Zijie Wang, Ke Wang, Haiwei Yang, Zhijian Han, Jun Tao, Hao Chen, Yuqiu Ge, Miao Guo, Chuanjian Suo, Ji-Fu Wei, Ruoyun Tan and Min Gu _

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Oncotarget. 2017; 8:100079-100094. https://doi.org/10.18632/oncotarget.21941

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Abstract

Zijie Wang1,*, Ke Wang1,*, Haiwei Yang1,*, Zhijian Han1, Jun Tao1, Hao Chen1, Yuqiu Ge2, Miao Guo3, Chuanjian Suo1, Ji-Fu Wei3, Ruoyun Tan1 and Min Gu1

1Department of Urology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China

2School of Public Health, Nanjing Medical University, Nanjing, China

3Research Division of Clinical Pharmacology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China

*These authors have contributed equally to this work

Correspondence to:

Min Gu, email: [email protected]

Ruoyun Tan, email: [email protected]

Keywords: kidney transplantation, antibody-mediated rejection, costimulatory signals, single-nucleotide polymorphisms next generation sequencing

Received: June 08, 2017     Accepted: August 19, 2017     Published: October 19, 2017

ABSTRACT

Antibody-mediated rejection (ABMR) is a serious complications that can occur following renal transplantation. The production of donor-specific antibodies by the humoral immune response can trigger costimulatory signals, which are crucial in activating immune cells, and therefore, playing a potential role in ABMR. To investigate the role of HVEM/LIGHT/BTLA/CD160 polymorphisms in ABMR, we retrospectively analyzed 200 renal transplant recipients. We adopted next-generation sequencing (NGS) to identify HVEM/LIGHT/BTLA/CD160 single-nucleotide polymorphisms (SNPs) in the genotypes of these patients. We divided the patients into two groups: those with ABMR and those who were stable. We adopted multiple models and performed regression analysis after adjusting for multiple confounding variables, to determine the correlation between the SNPs and ABMR. We obtained 41 high-quality SNPs readouts. However, we did not observe any significant association between these polymorphisms and the pathogenesis of ABMR in any of the models.Nevertheless, since there is evidence suggesting the involvement of costimulatory signals in graft rejection, further research should be conducted to better understand how genetic polymorphisms may be involved in ABMR.


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