| Literature DB >> 35219177 |
Thomas S C Ng1, Harris H Allen2, Mohammad Rashidian3, Miles A Miller4.
Abstract
Cancer immunotherapies typically aim to stimulate the accumulation and activity of cytotoxic T-cells or pro-inflammatory antigen-presenting cells, reduce immunosuppressive myeloid cells or regulatory T-cells, or elicit some combination of effects thereof. Notwithstanding the encouraging results, immunotherapies such as PD-1/PD-L1-targeted immune checkpoint blockade act heterogeneously across individual patients. It remains challenging to predict and monitor individual responses, especially across multiple sites of metastasis or sites of potential toxicity. To address this need, in vivo imaging of both adaptive and innate immune cell populations has emerged as a tool to quantify spatial leukocyte accumulation in tumors non-invasively. Here we review recent progress in the translational development of probes for in vivo leukocyte imaging, focusing on complementary perspectives provided by imaging of T-cells, phagocytic macrophages, and their responses to therapy.Entities:
Keywords: Adoptive cell therapy; Intravital microscopy; Magnetic resonance imaging; Positron emission tomography; Tumor associated macrophages; Tumor microenvironment
Mesh:
Year: 2022 PMID: 35219177 PMCID: PMC9118268 DOI: 10.1016/j.cbpa.2022.102117
Source DB: PubMed Journal: Curr Opin Chem Biol ISSN: 1367-5931 Impact factor: 8.972