Table 1.
Summary of preclinical ex vivo nanovehicle administration studies in transplantation.
Nano-vehicle | Method of Delivery | Therapeutic | Target Organ and Cell population | Results | Reference |
---|---|---|---|---|---|
ICAM-1-conjugated dextran-lysozyme nanogel adsorbed onto RBCs | Vascular perfusion | None | Human lung ECs | 3.7-fold higher localization to lung ECs than free nanocarriers | 160 |
Anti-CD31-conjugated PLA-PEG NP | NMP; whole organ/tissue immersion | None | Human kidney ECs | 5–10-fold higher localization to kidney ECs than isotype control Ab-conjugated NPs | 153 |
High-lactone poly(amine-co-ester) NP | NMP; whole organ/tissue immersion | siRNA targeting MHC class II transactivator | Human blood vessel ECs | Lowered MHC class II expression by ECs for 4–6 weeks; suppressed allogenic T cell responses | 161 |
Light-crosslinkable gelatin methacryloyl biomaterial | Whole organ/tissue immersion | Anti-IL-6R Ab | Mouse skin macrophages, T cells | Decreased alloreactive T cell and macrophage infiltration; doubled survival length of skin allografts | 164 |
PEG-PLGA NP | NMP; whole organ/tissue immersion | Anti-IL-6 Ab | Mouse heart macrophages, T cells | Decreased T cell and macrophage infiltration; inhibited chronic rejection in comparison to ischemic control | 167 |
PEG-PLGA NP | NMP; whole organ/tissue immersion | MMF | Mouse heart macrophages, T cells | Decreased expression of pro-inflammatory cytokine and chemokines; decreased T cell and macrophage infiltration; inhibited fibrosis and chronic rejection in comparison to free MMF | 35 |
ICAM-1: intercellular adhesion molecule-1; RBC: red blood cell; PLA: poly(lactic acid); NP: nanoparticle; PEG: polyethylene glycol; PLGA poly(lactic-co-glycolic) acid; siRNA: small inhibitory RNA; anti-IL-6R Ab: antibody against IL-6 receptor; anti-IL-6 Ab: antibody against IL-6; MMF: mycophenolate mofetil; EC: endothelial cell; MHC: major histocompatibility complex