W jaki spos贸b promieniowanie jonizuj膮ce przyczynia si臋 do wzbudzenia odporno艣ci na nowotw贸r?

tytu艂 oryg.: How does ionizing irradiation contribute to the induction of anti-tumor immunity?
Wydawnictwo: Frontiers in Oncology
Autor g艂贸wny:  Rainer Fietkau
Pozostali autorzy: Yvonne Rubner, RolandWunderlich, Paul-Friedrich R眉hle, Lorenz Kulzer, NinaWerthm枚ller, Benjamin Frey, Eva-MariaWeiss, Ludwig Keilholz, Udo S. Gaipl
Data: 2012-07-25

DOI: 10.3389/fonc.2012.00075

J臋zyk publikacji: angielski

Klasa publikacji: Artyku艂 przegl膮dowy

Typy skojarzenia HT omawiane w artykule: HT+RT

Abstract. Radiotherapy (RT) with ionizing irradiation is commonly used to locally attack tumors. It induces a stop of cancer cell proliferation and finally leads to tumor cell death. During the last years it has become more and more evident that besides a timely and locally restricted radiation-induced immune suppression, a specific immune activation against the tumor and its metastases is achievable by rendering the tumor cells visible for immune attack. The immune system is involved in tumor control and we here outline how RT induces antiinflammation when applied in lowdoses and contributes in higher doses to the induction of
anti-tumor immunity.We especially focus on how local irradiation induces abscopal effects. The latter are partly mediated by a systemic activation of the immune system against the individual tumor cells. Dendritic cells are the key players in the initiation and regulation of adaptive anti-tumor immune responses.They have to take up tumor antigens and consecutively present tumor peptides in the presence of appropriate co-stimulation.We review how combinations of RT with further immune stimulators such as AnnexinA5 and hyperthermia foster the dendritic cell-mediated induction of anti-tumor immune responses and present reasonable combination schemes of standard tumor therapies with immune therapies. It can be concluded that RT leads to targeted killing of the tumor cells and additionally induces non-targeted systemic immune effects. Multimodal tumor treatments should therefore tend to induce immunogenic tumor cell death forms within a tumor microenvironment that stimulates immune cells.

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