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

被引:384
|
作者
Duluc, Dorothee [1 ,10 ]
Delneste, Yves [1 ,10 ]
Tan, Fang [1 ,10 ]
Moles, Marie-Pierre [1 ,2 ,3 ,10 ]
Grimaud, Linda
Lenoir, Julien [1 ,2 ]
Preisser, Laurence
Anegon, Ignacio [4 ,5 ]
Catala, Laurent [6 ]
Ifrah, Norbert [2 ,3 ]
Descamps, Philippe [6 ]
Gamelin, Erick [1 ,7 ]
Gascan, Hugues [1 ]
Hebbar, Mohamed [8 ]
Jeannin, Pascale [1 ,9 ,10 ]
机构
[1] Univ Angers, Unite Rech Sante 564, Angers, France
[2] UPRES EA3863, Angers, France
[3] CHU Angers, Dept Malad Sang, Angers, France
[4] INSERM, UMR 643, Nantes, France
[5] Univ Nantes, Inst Transplantat & Rech Transplantat, FOCIS, Nantes, France
[6] CHU Angers, Dept Gynecol, Angers, France
[7] Ctr Lutte Contre Canc Paul Papin, Angers, France
[8] CHU Lille, Dept Oncol, F-59037 Lille, France
[9] CHU Angers, Lab Immunol & Allergol, Angers, France
[10] Ctr Hosp Univ, INSERM, Unit Equipe Avenir 564, F-49933 Angers, France
关键词
D O I
10.1182/blood-2007-02-072587
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Tumor-associated macrophages (TAMs), the most abundant immunosuppressive cells in the tumor microenvironment, originate from blood monocytes and exhibit an IL-10(high)IL-12(low) 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.
引用
收藏
页码:4319 / 4330
页数:12
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