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Arenavirus Induced CCL5 Expression Causes NK Cell-Mediated Melanoma Regression.
Bhat, Hilal; Zaun, Gregor; Hamdan, Thamer A; Lang, Judith; Adomati, Tom; Schmitz, Rosa; Friedrich, Sarah-Kim; Bergerhausen, Michael; Cham, Lamin B; Li, Fanghui; Ali, Murtaza; Zhou, Fan; Khairnar, Vishal; Duhan, Vikas; Brandenburg, Tim; Machlah, Yara Maria; Schiller, Maximilian; Berry, Arshia; Xu, Haifeng; Vollmer, Jörg; Häussinger, Dieter; Thier, Beatrice; Pandyra, Aleksandra A; Schadendorf, Dirk; Paschen, Annette; Schuler, Martin; Lang, Philipp A; Lang, Karl S.
Afiliación
  • Bhat H; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Zaun G; Department of Medical Oncology, West German Cancer Center, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
  • Hamdan TA; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Lang J; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Adomati T; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Schmitz R; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Friedrich SK; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Bergerhausen M; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Cham LB; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Li F; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Ali M; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Zhou F; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Khairnar V; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Duhan V; Department of Systems Biology, Beckman Research Institute, City of Hope, Monrovia, CA, United States.
  • Brandenburg T; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Machlah YM; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Schiller M; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Berry A; Medical Faculty, Institute of Immunology, University Duisburg-Essen, Essen, Germany.
  • Xu H; Department of Molecular Medicine II, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
  • Vollmer J; Department of Molecular Medicine II, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
  • Häussinger D; Abalos Therapeutics GmbH, Essen, Germany.
  • Thier B; Department of Gastroenterology, Hepatology and Infectious Diseases, University of Düsseldorf, Düsseldorf, Germany.
  • Pandyra AA; Department of Dermatology, University Hospital Essen, Essen, Germany.
  • Schadendorf D; Department of Molecular Medicine II, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
  • Paschen A; Department of Gastroenterology, Hepatology and Infectious Diseases, University of Düsseldorf, Düsseldorf, Germany.
  • Schuler M; Department of Dermatology, University Hospital Essen, Essen, Germany.
  • Lang PA; German Cancer Consortium (DKTK), Partner Site University Hospital Essen, Essen, Germany.
  • Lang KS; Department of Dermatology, University Hospital Essen, Essen, Germany.
Front Immunol ; 11: 1849, 2020.
Article en En | MEDLINE | ID: mdl-32973762
ABSTRACT
Immune activation within the tumor microenvironment is one promising approach to induce tumor regression. Certain viruses including oncolytic viruses such as the herpes simplex virus (HSV) and non-oncolytic viruses such as the lymphocytic choriomeningitis virus (LCMV) are potent tools to induce tumor-specific immune activation. However, not all tumor types respond to viro- and/or immunotherapy and mechanisms accounting for such differences remain to be defined. In our current investigation, we used the non-cytopathic LCMV in different human melanoma models and found that melanoma cell lines produced high levels of CCL5 in response to immunotherapy. In vivo, robust CCL5 production in LCMV infected Ma-Mel-86a tumor bearing mice led to recruitment of NK cells and fast tumor regression. Lack of NK cells or CCL5 abolished the anti-tumoral effects of immunotherapy. In conclusion, we identified CCL5 and NK cell-mediated cytotoxicity as new factors influencing melanoma regression during virotherapy.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Células Asesinas Naturales / Infecciones por Arenaviridae / Quimiocina CCL5 / Inmunoterapia / Melanoma Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Front Immunol Año: 2020 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Asunto principal: Células Asesinas Naturales / Infecciones por Arenaviridae / Quimiocina CCL5 / Inmunoterapia / Melanoma Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Front Immunol Año: 2020 Tipo del documento: Article País de afiliación: Alemania