Adipocytes Encapsulating Telratolimod Recruit and Polarize Tumor-Associated Macrophages for Cancer Immunotherapy

被引:20
|
作者
Wen, Di [1 ,2 ]
Liang, Tingxizi [1 ,4 ]
Chen, Guojun [1 ]
Li, Hongjun [1 ,4 ]
Wang, Zejun [1 ]
Wang, Jinqiang [1 ,4 ]
Fu, Ruxing [1 ]
Han, Xiao [1 ]
Ci, Tianyuan [1 ]
Zhang, Yuqi [1 ,4 ]
Abdou, Peter [1 ]
Li, Ruoxin [1 ]
Bu, Linlin [1 ]
Dotti, Gianpietro [3 ]
Gu, Zhen [1 ,4 ,5 ,6 ]
机构
[1] Univ Calif Los Angeles, Dept Bioengn, Los Angeles, CA 90095 USA
[2] Providence Portland Med Ctr, Earle A Chiles Res Inst, Robert W Franz Canc Ctr, Portland, OR 97213 USA
[3] Univ North Carolina Chapel Hill, Sch Med, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
[4] Zhejiang Univ, Coll Pharmaceut Sci, Key Lab Adv Drug Delivery Syst Zhejiang Prov, Hangzhou 310058, Peoples R China
[5] Zhejiang Univ, Jinhua Inst, Jinhua 321299, Peoples R China
[6] Zhejiang Univ, Sir Run Run Shaw Hosp, Sch Med, Dept Gen Surg, Hangzhou 310016, Peoples R China
关键词
adipocyte; cancer immunotherapy; drug delivery; macrophage; NECROSIS-FACTOR; CELLS; PROGRESSION; PROMOTE; TARGETS; TLR8;
D O I
10.1002/advs.202206001
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tumor-associated adipocytes (TAAs) recruit monocytes and promote their differentiation into tumor-associated macrophages (TAMs) that support tumor development. Here, TAAs are engineered to promote the polarization of TAMs to the tumor suppressive M1 phenotype. Telratolimod, a toll-like receptor 7/8 agonist, is loaded into the lipid droplets of adipocytes to be released at the tumor site upon tumor cell-triggered lipolysis. Locally administered drug-loaded adipocytes increased tumor suppressive M1 macrophages in both primary and distant tumors and suppressed tumor growth in a melanoma model. Furthermore, drug-loaded adipocytes improved CD8(+) T cell-mediated immune responses within the tumor microenvironment and favored dendritic cell maturation in the tumor draining lymph nodes.
引用
收藏
页数:9
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