Projects per year
Abstract / Description of output
Adoptive transfer of natural killer (NK) cells has been proposed as a novel immunotherapy for malignant tumours resistant to current therapeutic modalities. Several clinical studies have demonstrated that the NK cell-infusion is well tolerated without severe side effects and shows promising results in haematological malignancies. However, patients with malignant solid tumours do not show significant responses to this therapy. Such disappointing results largely arise from the inefficient delivery of infused NK cells and the impairment of their functions in the tumour microenvironment (TME). Tumour-associated macrophages (TAMs) are the most abundant stromal cells in the TME of most solid tumours, and a high TAM density correlates with poor prognosis of cancer patients. Although our knowledge of the interactions between TAMs and NK cells is limited, many studies have indicated that TAMs suppress NK cell cytotoxicity against cancer cells. Therefore, blockade of TAM functions can be an attractive strategy to improve NK cell-based immunotherapies. On the other hand, macrophages are reported to activate NK cells under certain circumstances. This essay presents our current knowledge about mechanisms by which macrophages regulate NK cell functions and discusses possible therapeutic approaches to block macrophage-mediated NK cell suppression.
Original language | English |
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Pages (from-to) | 1003-1014 |
Journal | Essays in biochemistry |
Volume | 67 |
Issue number | 6 |
Early online date | 14 Jun 2023 |
DOIs | |
Publication status | Published - 28 Sept 2023 |
Keywords / Materials (for Non-textual outputs)
- Humans
- Immunotherapy/methods
- Killer Cells, Natural
- Neoplasms/therapy
- Tumor Microenvironment
- Tumor-Associated Macrophages
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- 2 Finished
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Improvement of NK cell-infusion therapy for metastatic breast cancer by targeting tumour-associated macrophages
1/12/18 → 30/11/23
Project: Research
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MRC Centre for Reproductive Health at the University of Edinburgh
Pollard, J.
12/09/16 → 11/09/22
Project: Research