Major histocompatibility complex class i expression impacts on patient survival and type and density of immune cells in biliary tract cancer

  • Benjamin Goeppert
  • , Lena Frauenschuh
  • , Manuela Zucknick
  • , Stephanie Roessler
  • , Arianeb Mehrabi
  • , Mohammadreza Hafezi
  • , Albrecht Stenzinger
  • , Arne Warth
  • , Anita Pathil
  • , Marcus Renner
  • , Peter Schirmacher
  • , Wilko Weichert

Research output: Contribution to journalArticlepeer-review

59 Scopus citations

Abstract

Background:Biliary tract cancers (BTC) are rare malignant tumours with a poor prognosis. Previously, we have presented a detailed characterisation of the inflammatory infiltrate in BTC. Here, we analysed the impact of the expression of major histocompatibility complex class I (MHC I) on patient survival and the quantity, as well as the quality of tumour-infiltrating immune cell types in BTC.Methods:MHC I expression was assessed semi-quantitatively in 334 BTC, including extrahepatic (n=129) and intrahepatic cholangiocarcinomas (n=146), as well as adenocarcinomas of the gallbladder (n=59). In addition, 71 high-grade biliary intraepithelial lesions (BilIN 3) were included. Results were correlated with data on antitumour inflammation and investigated with respect to their association with clinicopathological variables and patient survival.Results:BTC showed a wide spectrum of different MHC I expression patterns ranging from complete negativity in some tumours to strong homogenous expression in others. In BilIN 3, significantly higher MHC I expression levels were seen compared to invasive tumours (P=0.004). Patients with strong tumoural MHC I expression had a significantly higher overall survival probability (median survival benefit: 8 months; P=0.006). MHC I expression strongly correlated with the number of tumour-infiltrating T-lymphocytes (CD4 + and CD8 +) and macrophages.Conclusions:Differences of MHC I expression predict patient outcome and show correlations with specific components of the inflammatory infiltrate in BTC. These findings contribute to a better understanding of immune response and immune escape phenomena in cholangiocarcinogenesis.

Original languageEnglish
Pages (from-to)1343-1349
Number of pages7
JournalBritish Journal of Cancer
Volume113
Issue number9
DOIs
StatePublished - 3 Nov 2015

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