Recently optimized technologies that permit the reversible opening of nanopores
across the red blood cell membrane, give the extraordinary opportunity
for reengineering human erythrocytes to be used in different biomedical applications,
both for therapeutic and diagnostic purposes. Engineered erythrocytes
have been exploited as a system for the controlled release of drugs in circulation
upon encapsulation of prodrugs or small molecules; as bioreactors when
they are endowed of recombinant enzymes able to catalyze the conversion of
toxic metabolite into inert products; as drug targeting system for the delivery of
compounds to the reticuloendothelial system inducing proper senescent signals
on the drug-loaded erythrocyte membrane; as carrier of contrasting agents for
diagnostic procedures. Preclinical development of these different applications
has taken advantage from the use of proper animal models whose erythrocytes
can be reengineered as the human ones or the encapsulation procedures can
be adapted on the basis of their specific erythrocyte biological features. Successful
results, obtained both in vitro and in preclinical studies, have prompted
several clinicians to start pilot clinical investigations in different conditions and
some new companies to start the industrialization of selected loading technologies
and to initiate clinical development programs. This short review summarizes
the key features that, to the best of our knowledge, have been crucial
to advance the products toward regulatory clinical approval making reengineering
of erythrocytes a modality to treat patients with limited or absent therapeutic
options
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