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Cancer Immune Therapy Edited by G. Stuhler and P. Walden ...

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216 10 The <strong>Immune</strong> System in <strong>Cancer</strong>: If It Isn't Broken, Can We Fix It?<br />

Fig. 10.5 How the immune system could be<br />

manipulated for effective antitumor immunotherapy.<br />

(A) What the immune system should<br />

not do: In autoimmune disease, it is believed<br />

that some initiating factor, e. g. viral or bacterial<br />

infection, serves as an adjuvant to initiate cell<br />

death of the target tissue. Antigen release occurs<br />

in the context of full immune activation. Molecular<br />

mimicry of a self antigen <strong>by</strong> a pathogenic<br />

antigen or direct activation of a potentially selfreactive<br />

T cell leads to activation of an autoimmune<br />

response from a small repertoire of such<br />

T cells. (B) What we would like the immune sys-<br />

tem to do. Effective immunotherapy strategies<br />

for cancer will combine elements from Figs<br />

10.4(A) <strong>and</strong> 10.5(A) (e. g. identification of foreign<br />

pathogens or autoimmune initiating agents<br />

along with gene transfer) to stimulate tumor cell<br />

killing <strong>and</strong> promote the creation of a highly immunostimulatory<br />

environment associated with<br />

release of tumor antigens. Although the antigens<br />

released will be predominantly self or near-self,<br />

they will be presented in a stimulatory fashion to<br />

a small pool of potentially reactive T cells that<br />

might have the ability to initiate <strong>and</strong> maintain<br />

antitumor immune responses.

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