Imaging and therapeutic targeting of the tumor immune microenvironment with biologics

被引:12
作者
Arnouk, Sana [1 ,2 ]
De Groof, Timo W. M. [3 ]
Van Ginderachter, Jo A. [1 ,2 ,4 ]
机构
[1] Vrije Univ Brussel, Cellular & Mol Immunol Lab, Brussels, Belgium
[2] VIB Ctr Inflammat Res, Myeloid Cell Immunol Lab, Brussels, Belgium
[3] Vrije Univ Brussel, Dept Med Imaging, In Vivo Cellular & Mol Imaging Lab, Brussels, Belgium
[4] Vrije Univ Brussel, Jo A Van Ginderachter Lab Cellular & Mol Immunol, Pl Laan 2, B-1050 Brussels, Belgium
关键词
Molecular imaging; Immunotherapy; Myeloid cells; T cells; Antibodies; Nanobodies; Tumor-associated macrophages; T-cell adoptive therapy; CAR T cells; POSITRON-EMISSION-TOMOGRAPHY; T-CELL THERAPY; MACROPHAGE MANNOSE RECEPTOR; PD-1 CHECKPOINT EXPRESSION; ANTIBODY FRAGMENTS; MEMBRANE ANTIGEN; PET; INHIBITION; RESPONSES; CANCER;
D O I
10.1016/j.addr.2022.114239
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The important role of tumor microenvironmental elements in determining tumor progression and metastasis has been firmly established. In particular, the presence and activity profile of tumor-infiltrating immune cells may be associated with the outcome of the disease and may predict responsiveness to (immuno)therapy. Indeed, while some immune cell types, such as macrophages, support cancer cell outgrowth and mediate therapy resistance, the presence of activated CD8+ T cells is usually indicative of a better prognosis. It is therefore of the utmost interest to obtain a full picture of the immune infiltrate in tumors, either as a prognostic test, as a way to stratify patients to maximize therapeutic success, or as therapy follow-up. Hence, the non-invasive imaging of these cells is highly warranted, with biologics being prime candidates to achieve this goal.(C) 2022 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http:// creativecommons.org/licenses/by/4.0/).
引用
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页数:13
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