Costa da Silva Milene, Breckwoldt Michael O, Vinchi Francesca, Correia Margareta P, Stojanovic Ana, Thielmann Carl Maximilian, Meister Michael, Muley Thomas, Warth Arne, Platten Michael, Hentze Matthias W, Cerwenka Adelheid, Muckenthaler Martina U
Department of Pediatric Oncology, Hematology and Immunology, University of Heidelberg, Heidelberg, Germany.
Molecular Medicine Partnership Unit (MMPU), Heidelberg University, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Front Immunol. 2017 Nov 8;8:1479. doi: 10.3389/fimmu.2017.01479. eCollection 2017.
Tumor-associated macrophages (TAMs) frequently help to sustain tumor growth and mediate immune suppression in the tumor microenvironment (TME). Here, we identified a subset of iron-loaded, pro-inflammatory TAMs localized in hemorrhagic areas of the TME. The occurrence of iron-loaded TAMs (iTAMs) correlated with reduced tumor size in patients with non-small cell lung cancer. experiments established that TAMs exposed to hemolytic red blood cells (RBCs) were converted into pro-inflammatory macrophages capable of directly killing tumor cells. This anti-tumor effect could also be elicited iron oxide nanoparticles. When tested , tumors injected with such iron oxide nanoparticles led to significantly smaller tumor sizes compared to controls. These results identify hemolytic RBCs and iron as novel players in the TME that repolarize TAMs to exert direct anti-tumor effector function. Thus, the delivery of iron to TAMs emerges as a simple adjuvant therapeutic strategy to promote anti-cancer immune responses.
肿瘤相关巨噬细胞(TAM)常常有助于维持肿瘤生长,并在肿瘤微环境(TME)中介导免疫抑制。在此,我们鉴定出了位于TME出血区域的一组富含铁、具有促炎作用的TAM。富含铁的TAM(iTAM)的出现与非小细胞肺癌患者肿瘤体积减小相关。实验证实,暴露于溶血红细胞(RBC)的TAM会转变为能够直接杀伤肿瘤细胞的促炎巨噬细胞。这种抗肿瘤效应也可由氧化铁纳米颗粒引发。在进行测试时,与对照组相比,注射了此类氧化铁纳米颗粒的肿瘤体积显著更小。这些结果表明,溶血RBC和铁是TME中的新参与者,它们可使TAM重新极化以发挥直接的抗肿瘤效应功能。因此,向TAM递送铁成为一种促进抗癌免疫反应的简单辅助治疗策略。