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Serum proteomic profiling and haptoglobin polymorphisms in patients with GVHD after allogeneic hematopoietic cell transplantation

  • Joseph Mcguirk
  • , Gang Hao
  • , Weijian Hou
  • , Sunil Abhyankar
  • , Casey Williams
  • , Weisi Yan
  • , Jianda Yuan
  • , Xiuqin Guan
  • , Robert Belt
  • , Shaun Dejarnette
  • , Jeffery Wieman
  • , Ying Yan

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

We studied serum proteomic profiling in patients with graft versus host disease (GVHD) after allogeneic hematopoietic cell transplantation (allo-HCT) by two-dimensional gel electrophoresis (2-DE) and mass spectrometry analysis. The expression of a group of proteins, haptoglobin (Hp), alpha-1-antitrypsin, apolipoprotein A-IV, serum paraoxonase and Zn-alpha-glycoprotein were increased and the proteins, clusterin precursor, alpha-2-macroglobulin, serum amyloid protein precursor, sex hormone-binding globulin, serotransferrin and complement C4 were decreased in patients with extensive chronic GVHD (cGVHD). Serum haptoglobin (Hp) levels in patients with cGVHD were demonstrated to be statistically higher than in patients without cGVHD and normal controls (p<0.01). We used immunoblotting and PCR in combination with 2-DE gel image analysis to determine Hp polymorphisms in 25 allo-HCT patients and 16 normal donors. The results demonstrate that patients with cGVHD had a higher incidence of HP 2-2 phenotype (43.8%), in comparison to the patients without cGVHD (0%) and normal donors (18.7%), suggesting the possibility that specific Hp polymorphism may play a role in the development of cGVHD after allo-HCT. In this study, quantitative serum Hp levels were shown to be related to cGVHD development. Further, the data suggest the possibility that specific Hp polymorphisms may be associated with cGVHD development and warrant further investigation.

Original languageEnglish
Article number17
JournalJournal of Hematology and Oncology
Volume2
DOIs
StatePublished - 2009

Funding

This study is supported by the grants from Saint Luke's Research Foundation and Glass Family Cancer Research Foundation. We thank Dr. Jianfeng Liu for statistics assistance and Sue Latham for the research project coordination.

Funders
Glass Family Cancer Research Foundation
Saint Luke's Research Foundation

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    ASJC Scopus subject areas

    • Hematology
    • Molecular Biology
    • Oncology
    • Cancer Research

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