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Table 4 Application of immune cells based on DDS in AD

From: Immune cells: potential carriers or agents for drug delivery to the central nervous system

Immune cells

Components

Loaded drugs/nanoparticles

Methods

Model

Functions

References

Monocyte

Cell

Nerve growth factor

Trojan horse

Brain capillary endothelial cell monolayer

Migrate into brain slices

[183]

Macrophage

Exosomes

Curcumin

Incubation and ultracentrifugal separation (pre-loading)

Stereotaxic-induced AD model

Target BBB and hippocampal nerve cells

Inhibit hyperphosphorylation of Tau protein

Ameliorate cognitive function

[184]

 

Exosomes

Silibinin

Incubation and differential ultracentrifugal separation (pre-loading)

Aβ1-42-induced AD model

Inhibition of Aβ aggregation

Activate astrocytes

Alleviate cognitive impairment

[186]

 

RVG/TPP-modified membrane

MASLNs

Hypotonic lysis and centrifugal separation; Co-extrusion

APP/PS1 mice

Target BBB and neuronal mitochondria

[187]

Microglia

Mannose-modified EVs

Gemfibrozil

Incubation and gradient centrifugation separation (pre-loading)

Aβ1-42-induced AD model

Target BBB and microglia

Facilitate Aβ clearance via enhancing activity of microglial lysosome; Promoting cognitive recovery

[185]

DC cell

Lamp2b overexpressing and RVG-fused exosomes

siRNA

Differential centrifugal separation and electroporation (post-loading)

BACE1 knockdown model mice

Target BBB, neurons, microglia, and oligodendrocytes

Decrease amyloid plaques

Induce immune responses

[59]

  1. AD Alzheimer’s disease, Aβ amyloid-β, APP/PS1 APPswe/PSEN1dE9, BACE1 β-secretase 1, BBB blood–brain barrier, EVs extracellular vesicles, MASLNs macrophage membrane-coated solid lipid nanoparticles, RVG rabies virus glycoprotein, TPP triphenylphosphine