4.6 Article

The paradoxical changes of membrane and soluble herpes virus entry mediator in hepatocellular carcinoma patients

期刊

JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY
卷 32, 期 8, 页码 1520-1524

出版社

WILEY
DOI: 10.1111/jgh.13678

关键词

hepatocellular carcinoma; HVEM; lymphocytes; soluble HVEM

资金

  1. Pearl River S&T Nova Program of Guangzhou [201605122020199]
  2. Natural Science Fund of Guangdong Province [2014A030313089, S2013010016014]
  3. Medical Scientific Research Foundation of Guangdong Province [A2014237]
  4. NSFC [81202319, 81370535, 81570539]
  5. Specialized Research Fund for the Doctoral Program of Higher Education [20120171120107]

向作者/读者索取更多资源

Background and Aim: The herpes virus entry mediator (HVEM) network has become new directions in targeting novel checkpoint inhibitors for cancer therapy. However, the changes of membrane-bound HVEM (mHVEM) and soluble HVEM (sHVEM) in hepatocellular carcinoma (HCC) are not fully understood. This study aims to study the changes of mHVEM and sHVEM in HCC patients. Methods: Serum samples were collected from 65 HCC patients, from which sHVEM levels were examined by enzyme-linked immunosorbent assay. Expressions of mHVEM on peripheral lymphocytes from 20 HCC patients were determined using flow cytometry, and associations between mHVEM on T and B cells were analyzed. Results: The levels of mHVEM were downregulated on peripheral lymphocytes in HCC patients, with a strong positive correlation between mHVEM expression on T and B cells. In contrast, the levels of soluble HVEM were upregulated in the serum of HCC patients. Furthermore, we found that the increase in sHVEM level was correlated with advanced stages HCC. Conclusion: Our data demonstrated paradoxical changes of membrane and soluble HVEM in the peripheral blood of HCC patients for the first time. These data supported the notion that roles of HVEM are likely to be immunosuppressive rather than activating tumor immunity. Future studies are warranted to further explore the translational values of mHVEM and sHVEM in peripheral blood as diagnostic markers and therapeutic targets.

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