Abstract

Red blood cells (RBC) are actually exploited as innovative drug delivery systems with unconventional and convenient properties. Because of a long in vivo survival and a non-random removal from circulation, RBC can be loaded with drugs and/or contrasting agents without affecting these properties and maintaining the original immune competence. However, native or drug-loaded RBC, can be modified decorating the membrane with peptides, antibodies or small chemical entities so favoring the targeting of the processed RBC to specific cells or organs. Convenient modifications have been exploited to induce immune tolerance or immunogenicity, to deliver antibodies capable of targeting other cells, and to deliver a number of constructs that can recognize circulating pathogens or toxins. The methods used to induce membrane processing useful for biomedical applications include the use of crosslinking agents and bifunctional antibodies, biotinylation and membrane insertion. Another approach includes the expression of engineered membrane proteins upon ex vivo transfection of immature erythroid precursors with lentiviral vectors, followed by in vitro expansion and differentiation into mature erythrocytes before administration to a patient in need. Several applications have now reached the clinic and a couple of companies that take advantage from these properties of RBC are already in Phase 3 with selected applications. The peculiar properties of the RBC and the active research in this field by a number of qualified investigators, have opened new exciting perspectives on the use of RBC as carriers of drugs or as cellular therapeutics.

Highlights

  • For many years, drug-loaded red blood cells (RBC) have been exploited as delivery systems for the release in circulation of active agents, for the increase in the life-span in circulation of therapeutic agents, for the protection by immune inactivation of therapeutic enzymes, and for a prolonged circulation of contrasting agents useful in diagnostic applications

  • These requirements are mandatory to prevent the release of the encapsulated drugs, to preserve the Red blood cells (RBC) immunogenicity avoiding the induction of anti-carrier immune responses and to maintain native phospholipid asymmetry preventing RBC clearance by macrophages

  • Others and we have reported that RBC can perform as antigen delivery systems inducing an immunological response that overcomes the use of adjuvants (Magnani et al, 1992b; Chiarantini et al, 1997)

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Summary

Introduction

Drug-loaded red blood cells (RBC) have been exploited as delivery systems for the release in circulation of active agents, for the increase in the life-span in circulation of therapeutic agents, for the protection by immune inactivation of therapeutic enzymes, and for a prolonged circulation of contrasting agents useful in diagnostic applications (reviewed in Rossi et al, 2016; Villa et al, 2016; Pierigè et al, 2017). RBC can be conveniently modified, covalently or non-covalently, to deliver membrane bound therapeutic agents but target specificity, number of target sites on the RBC membrane, and the resulting effect of coupling the therapeutic agent must be carefully investigated to prevent RBC damage and hemolysis and/or fast removal from circulation.

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