Opposite Macrophage Polarization in Different Subsets of Ovarian Cancer: Observation from a Pilot Study

The role of the innate immune system in ovarian cancer is gaining importance. The relevance of tumor-associated macrophages (TAM) is insufficiently understood. In this pilot project, comprising the immunofluorescent staining of 30 biopsies taken from 24 patients with ovarian cancer, we evaluated the...

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Main Authors: Ann Vankerckhoven, Roxanne Wouters, Thomas Mathivet, Jolien Ceusters, Thaïs Baert, Anaïs Van Hoylandt, Holger Gerhardt, Ignace Vergote, An Coosemans
Format: Article
Language:English
Published: MDPI AG 2020-01-01
Series:Cells
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Online Access:https://www.mdpi.com/2073-4409/9/2/305
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author Ann Vankerckhoven
Roxanne Wouters
Thomas Mathivet
Jolien Ceusters
Thaïs Baert
Anaïs Van Hoylandt
Holger Gerhardt
Ignace Vergote
An Coosemans
author_facet Ann Vankerckhoven
Roxanne Wouters
Thomas Mathivet
Jolien Ceusters
Thaïs Baert
Anaïs Van Hoylandt
Holger Gerhardt
Ignace Vergote
An Coosemans
author_sort Ann Vankerckhoven
collection DOAJ
description The role of the innate immune system in ovarian cancer is gaining importance. The relevance of tumor-associated macrophages (TAM) is insufficiently understood. In this pilot project, comprising the immunofluorescent staining of 30 biopsies taken from 24 patients with ovarian cancer, we evaluated the presence of total TAM (cluster of differentiation (CD) 68 expression), M1 (major histocompatibility complex (MHC) II expression), and M2 (anti-mannose receptor C type 1 (MRC1) expression), and the blood vessel diameter. We observed a high M1/M2 ratio in low-grade ovarian cancer compared to high-grade tumors, more total TAM and M2 in metastatic biopsies, and a further increase in total TAM and M2 at interval debulking, without beneficial effects of bevacizumab. The blood vessel diameter was indicative for M2 tumor infiltration (Spearman correlation coefficient of 0.65). These data mainly reveal an immune beneficial environment in low-grade ovarian cancer in contrast to high-grade serous ovarian cancer, where immune suppression is not altered by neoadjuvant therapy.
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spelling doaj.art-8e28886361f141a2a9f7334a1fbc62f12023-08-02T04:08:22ZengMDPI AGCells2073-44092020-01-019230510.3390/cells9020305cells9020305Opposite Macrophage Polarization in Different Subsets of Ovarian Cancer: Observation from a Pilot StudyAnn Vankerckhoven0Roxanne Wouters1Thomas Mathivet2Jolien Ceusters3Thaïs Baert4Anaïs Van Hoylandt5Holger Gerhardt6Ignace Vergote7An Coosemans8ImmunOvar Research Group, Laboratory of Tumor Immunology and Immunotherapy, Department of Oncology, KU Leuven, 3000 Leuven, BelgiumImmunOvar Research Group, Laboratory of Tumor Immunology and Immunotherapy, Department of Oncology, KU Leuven, 3000 Leuven, BelgiumPARCC, HEGP Institute (team 9), INSERM U970, Université Paris Descartes, 75006 Paris, FranceImmunOvar Research Group, Laboratory of Tumor Immunology and Immunotherapy, Department of Oncology, KU Leuven, 3000 Leuven, BelgiumImmunOvar Research Group, Laboratory of Tumor Immunology and Immunotherapy, Department of Oncology, KU Leuven, 3000 Leuven, BelgiumImmunOvar Research Group, Laboratory of Tumor Immunology and Immunotherapy, Department of Oncology, KU Leuven, 3000 Leuven, BelgiumVascular Patterning Lab, Center for Cancer Biology, VIB, KU Leuven, 3000 Leuven, BelgiumImmunOvar Research Group, Laboratory of Tumor Immunology and Immunotherapy, Department of Oncology, KU Leuven, 3000 Leuven, BelgiumImmunOvar Research Group, Laboratory of Tumor Immunology and Immunotherapy, Department of Oncology, KU Leuven, 3000 Leuven, BelgiumThe role of the innate immune system in ovarian cancer is gaining importance. The relevance of tumor-associated macrophages (TAM) is insufficiently understood. In this pilot project, comprising the immunofluorescent staining of 30 biopsies taken from 24 patients with ovarian cancer, we evaluated the presence of total TAM (cluster of differentiation (CD) 68 expression), M1 (major histocompatibility complex (MHC) II expression), and M2 (anti-mannose receptor C type 1 (MRC1) expression), and the blood vessel diameter. We observed a high M1/M2 ratio in low-grade ovarian cancer compared to high-grade tumors, more total TAM and M2 in metastatic biopsies, and a further increase in total TAM and M2 at interval debulking, without beneficial effects of bevacizumab. The blood vessel diameter was indicative for M2 tumor infiltration (Spearman correlation coefficient of 0.65). These data mainly reveal an immune beneficial environment in low-grade ovarian cancer in contrast to high-grade serous ovarian cancer, where immune suppression is not altered by neoadjuvant therapy.https://www.mdpi.com/2073-4409/9/2/305ovarian cancermacrophagesm2
spellingShingle Ann Vankerckhoven
Roxanne Wouters
Thomas Mathivet
Jolien Ceusters
Thaïs Baert
Anaïs Van Hoylandt
Holger Gerhardt
Ignace Vergote
An Coosemans
Opposite Macrophage Polarization in Different Subsets of Ovarian Cancer: Observation from a Pilot Study
Cells
ovarian cancer
macrophages
m2
title Opposite Macrophage Polarization in Different Subsets of Ovarian Cancer: Observation from a Pilot Study
title_full Opposite Macrophage Polarization in Different Subsets of Ovarian Cancer: Observation from a Pilot Study
title_fullStr Opposite Macrophage Polarization in Different Subsets of Ovarian Cancer: Observation from a Pilot Study
title_full_unstemmed Opposite Macrophage Polarization in Different Subsets of Ovarian Cancer: Observation from a Pilot Study
title_short Opposite Macrophage Polarization in Different Subsets of Ovarian Cancer: Observation from a Pilot Study
title_sort opposite macrophage polarization in different subsets of ovarian cancer observation from a pilot study
topic ovarian cancer
macrophages
m2
url https://www.mdpi.com/2073-4409/9/2/305
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