Although considerable efforts have been made in the discovery of new agents for cancer treatment, several promising
therapeutics cannot be applied systemically because of their severe side effects. This is the case for various recombinant
pro-inflammatory cytokines that, despite their potent anti-cancer activity, cannot find their way to clinical exploitation
due to their devastating toxicity shown during dose escalation to therapeutically active concentrations. To circumvent
these problems, an elegant and efficient way to accumulate therapeutic agents at the tumor site, thus reducing systemic
side effects, is their conjugation to tumor-specific antibodies. Here, we review preclinical data about immunocytokines
conjugated to a promising single-chain human antibody that selectively targets tumor-associated stroma and blood
vessels by binding with high affinity and specificity to the extradomain-B(EDB) of fibronectin
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