Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid Stoffw Microb

Atanasov, G; Dino, K; Schierle, K; Dietel, C; Aust, G; Pratschke, J; Seehofer, D; Schmelzle, M; Hau, HM.
Recipient Hepatic Tumor-Associated Immunologic Infiltrates Predict Outcomes After Liver Transplantation for Hepatocellular Carcinoma.
Ann Transplant. 2020; 25: e919414 Doi: 10.12659/AOT.919414 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Co-Autor*innen der Med Uni Graz
Hau Hans-Michael
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
BACKGROUND Transplantation of the liver entails a state of altered recipient immunologic competence. There are only scarce data concerning the impact of host immunologic factors on the outcome of liver transplant recipients in the context of hepatocellular carcinoma (HCC). MATERIAL AND METHODS Our study focused on evaluating the presence of tumor necrosis and frequency levels of angiopoietins and monocytes/macrophages subtypes in the host liver prior to liver transplantation (LTX) and their association with recurrence, graft rejection, survival, and clinical prognosis after LTX. Formation of tumor necrosis and tissue densities of angiopoietins and cellular immunologic infiltrates - CD68⁺ and CD163⁺ macrophages (TAMs) and TIE2-expressing monocytes (TEMs) - were quantified in recipient HCC specimens. The densities were then matched with clinicopathologic variables and patient survival after LTX (n=88). Some patients were treated prior to LTX by neoadjuvant transarterial chemoembolization (TACE, n=55). RESULTS Recipient hepatic infiltration with TEMs and CD68⁺ TAMs was associated with decreased 1-, 3-, and 5-year survival, as well as metastatic and recurrent HCC after LTX (all p<0.05). TEMs and infiltrating monocytes/macrophages were associated with angiopoietin expression, metastatic, and recurrent HCC (all p<0.05). Furthermore, hepatic angiopoietin-2 expression was associated with graft rejection after LTX (p<0.05). After TACE and LTX, formation of tumor necrosis was associated with an increased presence of monocytes/macrophages and a reduced incidence of recurrent HCC in the graft (all p<0.05). CONCLUSIONS Infiltrating monocytes/macrophages subsets and related angiopoietin axis are associated with worse survival, tumor recurrence, and clinical outcome after LTX for HCC.
Find related publications in this database (using NLM MeSH Indexing)
Angiopoietins - metabolism
Carcinoma, Hepatocellular - metabolism, pathology, surgery
Female - administration & dosage
Graft Rejection - metabolism, pathology
Graft Survival - administration & dosage
Humans - administration & dosage
Liver - metabolism, pathology
Liver Neoplasms - metabolism, pathology, surgery
Liver Transplantation - administration & dosage
Macrophages - metabolism, pathology
Male - administration & dosage
Middle Aged - administration & dosage
Monocytes - metabolism, pathology
Prognosis - administration & dosage
Treatment Outcome - administration & dosage
Tumor Microenvironment - physiology

Find related publications in this database (Keywords)
Angiopoietins
Carcinoma, Hepatocellular
Liver Transplantation
Monocytes
© Med Uni Graz Impressum