TUMOR-SPECIFIC IMMUNE RESPONSE AFTER PHOTODYNAMIC THERAPY

Increased incidence of malignancies requires a search for new therapeutic approaches. E.g., photodynamic therapy (PDT) is an effective anti-cancer treatment that involves administration of a photosensitizing dye followed by visible light irradiation of the tumor. Pre-clinical studies have shown that...

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Autores principales: Yu. N. Anokhin, E. V. Abakushina
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Lenguaje:RU
Publicado: SPb RAACI 2016
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spelling oai:doaj.org-article:3a36ed1f33f4446a99b18f843de71d472021-11-18T08:03:45ZTUMOR-SPECIFIC IMMUNE RESPONSE AFTER PHOTODYNAMIC THERAPY1563-06252313-741X10.15789/1563-0625-2016-5-405-416https://doaj.org/article/3a36ed1f33f4446a99b18f843de71d472016-08-01T00:00:00Zhttps://www.mimmun.ru/mimmun/article/view/1063https://doaj.org/toc/1563-0625https://doaj.org/toc/2313-741XIncreased incidence of malignancies requires a search for new therapeutic approaches. E.g., photodynamic therapy (PDT) is an effective anti-cancer treatment that involves administration of a photosensitizing dye followed by visible light irradiation of the tumor. Pre-clinical studies have shown that local photodynamic therapy enhances systemic antitumor immunity. Moreover, it is well known that the long-term effects of PDT depend on functioning of intact adaptive immune response. In this context, the immune system plays a fundamental role. Interestingly, the PDT action is associated with stimulation of systemic immune response against a locally treated tumor. In fact, PDT has been shown to effectively stimulate both innate and adaptive immune systems of the host, by triggering the release of various pro-inflammatory and acutephase response mediators thus leading to massive infiltration of the treated site with neutrophils, dendritic cells and other inflammatory cells. PDT efficacy depends, in part, on induction of tumor-specific immune response which is dependent on cytotoxic T lymphocytes and natural killer (NK) cells. The set of specific receptors enables NK cells to recognize surface molecules on the target cells. Expression of the latter molecules is indicative of viral infection, tumor formation, or cell stress (e.g., DNA damage). The NK cells are also involved into various biological processes in the organism, playing a critical role in immune surveillance, thus representing a potential tool for cancer therapy. It was shown that the tumor cells have increased sensitivity to NK cell-mediated lytic action following PDT. In this review, we further discuss potential relationships between PDT and antitumor immune response.Yu. N. AnokhinE. V. AbakushinaSPb RAACIarticlephotodynamic therapycancerantitumor immune responsenatural killer cellsmicankg2d moleculeslymphocyte activationImmunologic diseases. AllergyRC581-607RUMedicinskaâ Immunologiâ, Vol 18, Iss 5, Pp 405-416 (2016)
institution DOAJ
collection DOAJ
language RU
topic photodynamic therapy
cancer
antitumor immune response
natural killer cells
mica
nkg2d molecules
lymphocyte activation
Immunologic diseases. Allergy
RC581-607
spellingShingle photodynamic therapy
cancer
antitumor immune response
natural killer cells
mica
nkg2d molecules
lymphocyte activation
Immunologic diseases. Allergy
RC581-607
Yu. N. Anokhin
E. V. Abakushina
TUMOR-SPECIFIC IMMUNE RESPONSE AFTER PHOTODYNAMIC THERAPY
description Increased incidence of malignancies requires a search for new therapeutic approaches. E.g., photodynamic therapy (PDT) is an effective anti-cancer treatment that involves administration of a photosensitizing dye followed by visible light irradiation of the tumor. Pre-clinical studies have shown that local photodynamic therapy enhances systemic antitumor immunity. Moreover, it is well known that the long-term effects of PDT depend on functioning of intact adaptive immune response. In this context, the immune system plays a fundamental role. Interestingly, the PDT action is associated with stimulation of systemic immune response against a locally treated tumor. In fact, PDT has been shown to effectively stimulate both innate and adaptive immune systems of the host, by triggering the release of various pro-inflammatory and acutephase response mediators thus leading to massive infiltration of the treated site with neutrophils, dendritic cells and other inflammatory cells. PDT efficacy depends, in part, on induction of tumor-specific immune response which is dependent on cytotoxic T lymphocytes and natural killer (NK) cells. The set of specific receptors enables NK cells to recognize surface molecules on the target cells. Expression of the latter molecules is indicative of viral infection, tumor formation, or cell stress (e.g., DNA damage). The NK cells are also involved into various biological processes in the organism, playing a critical role in immune surveillance, thus representing a potential tool for cancer therapy. It was shown that the tumor cells have increased sensitivity to NK cell-mediated lytic action following PDT. In this review, we further discuss potential relationships between PDT and antitumor immune response.
format article
author Yu. N. Anokhin
E. V. Abakushina
author_facet Yu. N. Anokhin
E. V. Abakushina
author_sort Yu. N. Anokhin
title TUMOR-SPECIFIC IMMUNE RESPONSE AFTER PHOTODYNAMIC THERAPY
title_short TUMOR-SPECIFIC IMMUNE RESPONSE AFTER PHOTODYNAMIC THERAPY
title_full TUMOR-SPECIFIC IMMUNE RESPONSE AFTER PHOTODYNAMIC THERAPY
title_fullStr TUMOR-SPECIFIC IMMUNE RESPONSE AFTER PHOTODYNAMIC THERAPY
title_full_unstemmed TUMOR-SPECIFIC IMMUNE RESPONSE AFTER PHOTODYNAMIC THERAPY
title_sort tumor-specific immune response after photodynamic therapy
publisher SPb RAACI
publishDate 2016
url https://doaj.org/article/3a36ed1f33f4446a99b18f843de71d47
work_keys_str_mv AT yunanokhin tumorspecificimmuneresponseafterphotodynamictherapy
AT evabakushina tumorspecificimmuneresponseafterphotodynamictherapy
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