Ionizing radiation can affect the immune system in many ways. Depending on the
situation, the whole body or parts of the body can be acutely or chronically exposed to
different radiation qualities. In tumor radiotherapy, a fractionated exposure of the tumor
(and surrounding tissues) is applied to kill the tumor cells. Currently, mostly photons, and
also electrons, neutrons, protons, and heavier particles such as carbon ions, are used
in radiotherapy. Tumor elimination can be supported by an effective immune response.
In recent years, much progress has been achieved in the understanding of basic interactions
between the irradiated tumor and the immune system. Here, direct and indirect
effects of radiation on immune cells have to be considered. Lymphocytes for example
are known to be highly radiosensitive. One important factor in indirect interactions is
the radiation-induced bystander effect which can be initiated in unexposed cells by
expression of cytokines of the irradiated cells and by direct exchange of molecules via
gap junctions. In this review, we summarize the current knowledge about the indirect
effects observed after exposure to different radiation qualities. The different immune cell
populations important for the tumor immune response are natural killer cells, dendritic
cells, and CD8+ cytotoxic T-cells. In vitro and in vivo studies have revealed the modulation
of their functions due to ionizing radiation exposure of tumor cells. After radiation
exposure, cytokines are produced by exposed tumor and immune cells and a modulated
expression profile has also been observed in bystander immune cells. Release
of damage-associated molecular patterns by irradiated tumor cells is another factor in
immune activation. In conclusion, both immune-activating and -suppressing effects can
occur. Enhancing or inhibiting these effects, respectively, could contribute to modified
tumor cell killing after radiotherapy
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