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

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10.5 Playing to Strengths<br />

cell death of infected cells <strong>and</strong> cytokine-rich environments created <strong>by</strong> reactivity<br />

against the antigens (Fig. 10.4A). There is also likely to be a large number of naive T<br />

cells with TCR specificities that can bind epitopes from the immunogens when presented<br />

<strong>by</strong> APCs (Fig. 10.3). The APCs will also have been activated <strong>by</strong> the inflammatory<br />

milieu. This will provide high levels of co-stimulatory molecules in association<br />

with which the antigenic epitopes will be presented to the T cells ± resulting in a vigorous<br />

<strong>and</strong> potent clearative response (Fig. 10.4A).<br />

In the case of tumor cell recognition (Fig. 10.4B), however, the repertoire of antigenic<br />

targets is far less clearly defined <strong>and</strong> is much more subversive [8]. Until the tumor<br />

develops a necrotic core, which occurs when its growth has outstripped its blood<br />

supply, there is minimal cell death occurring <strong>and</strong> few tumor antigens are released,<br />

213

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