Radiation therapy and the innate immune response: Clinical implications for immunotherapy approaches
Radiation therapy is an essential component of cancer care, contributing up to 40% of curative cancer treatment regimens. It creates DNA double‐strand breaks causing cell death in highly replicating tumour cells. However, tumours can develop acquired resistance to therapy. The efficiency of radiatio...
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Published in: | British journal of clinical pharmacology Vol. 86; no. 9; pp. 1726 - 1735 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
England
John Wiley and Sons Inc
01-09-2020
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Subjects: | |
Online Access: | Get full text |
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Summary: | Radiation therapy is an essential component of cancer care, contributing up to 40% of curative cancer treatment regimens. It creates DNA double‐strand breaks causing cell death in highly replicating tumour cells. However, tumours can develop acquired resistance to therapy. The efficiency of radiation treatment has been increased by means of combining it with other approaches such as chemotherapy, molecule‐targeted therapies and, in recent years, immunotherapy (IT).
Cancer‐cell apoptosis after radiation treatment causes an immunological reaction that contributes to eradicating the tumour via antigen presentation and subsequent T‐cell activation. By contrast, radiotherapy also contributes to the formation of an immunosuppressive environment that hinders the efficacy of the therapy. Innate immune cells from myeloid and lymphoid origin show a very active role in both acquired resistance and antitumourigenic mechanisms. Therefore, many efforts are being made in order to reach a better understanding of the innate immunity reactions after radiation therapy (RT) and the design of new combinatorial IT strategies focused in these particular populations. |
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Bibliography: | Valentí Gómez, Rami Mustapha and Kenrick Ng contributed equally to this work. ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 Valentí Gómez, Rami Mustapha and Kenrick Ng contributed equally to this work. |
ISSN: | 0306-5251 1365-2125 |
DOI: | 10.1111/bcp.14351 |