Tumor-associated leukemia inhibitory factor and IL-6 skew monocyte differentiation into tumor-associated macrophage-like cells

Author:

Duluc Dorothée12,Delneste Yves12,Tan Fang12,Moles Marie-Pierre1234,Grimaud Linda25,Lenoir Julien3,Preisser Laurence25,Anegon Ignacio67,Catala Laurent8,Ifrah Norbert34,Descamps Philippe8,Gamelin Erick259,Gascan Hugues25,Hebbar Mohamed10,Jeannin Pascale1211

Affiliation:

1. Inserm, U564, Equipe Avenir, Angers;

2. Université d'Angers, Unité Mixte de Recherche–Santé (UMR-S) 564, Angers;

3. Université d'Angers, Unité Propre de Recherche de l'Enseignement Supérieur (UPRES) EA3863, Angers;

4. Centre Hospitalier Universitaire (CHU) d'Angers, Département des maladies du sang, Angers;

5. Inserm, U564, Angers;

6. Inserm UMR 643, Nantes;

7. Université de Nantes, Institut de Transplantation et de Recherche en Transplantation, Federation of Clinical Immunology Societies (FOCIS), Nantes;

8. CHU d'Angers, Département de Gynécologie, Angers;

9. Centre de lutte contre le Cancer Paul Papin, Angers;

10. CHU de Lille, Département d'Oncologie, Lille; and

11. CHU d'Angers, Laboratoire d'Immunologie et d'Allergologie, Angers, France

Abstract

Tumor-associated macrophages (TAMs), the most abundant immunosuppressive cells in the tumor microenvironment, originate from blood monocytes and exhibit an IL-10highIL-12low M2 profile. The factors involved in TAM generation remain unidentified. We identify here leukemia inhibitory factor (LIF) and IL-6 as tumor microenvironmental factors that can promote TAM generation. Ovarian cancer ascites switched monocyte differentiation into TAM-like cells that exhibit most ovarian TAM functional and phenotypic characteristics. Ovarian cancer ascites contained high concentrations of LIF and IL-6. Recombinant LIF and IL-6 skew monocyte differentiation into TAM-like cells by enabling monocytes to consume monocyte–colony-stimulating factor (M-CSF). Depletion of LIF, IL-6, and M-CSF in ovarian cancer ascites suppressed TAM-like cell induction. We extended these observations to different tumor-cell line supernatants. In addition to revealing a new tumor-escape mechanism associated with TAM generation via LIF and IL-6, these findings offer novel therapeutic perspectives to subvert TAM-induced immunosuppression and hence improve T-cell–based antitumor immunotherapy efficacy.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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