Skip to main content

Table 3 Representative nanomaterials in treating HMs that stimulate the immune system

From: Development and application of nanomaterials, nanotechnology and nanomedicine for treating hematological malignancies

Nanomaterials

Payload

Ind.

Outcome

References

PLA microspheres

PD-1 antibody and leukemia antigen polypeptide pE

Leu

Enhance the APC response, recruit more APC cells, enhance the proliferation of T cells in lymph nodes

[167]

Hydrogel

Antigen polypeptide WT1126-134 and immune adjuvants (GM-CSF)

Leu

Induce local immune-cell infiltration and activate dendritic cells

[166]

LNT cells

DOX

Leu

Promote antitumor immune responses

[171]

HSCs

aPD-1

Leu

Increase the number of active T cells, produce cytokines and chemokines

[172]

Lipid-PEG

mRNA, palmitic acid-modified TLR7/8 agonist R848 (C16-R848)

Lyn

Improve the expansion of OVA specific CD8 + T cells

[168]

PLGA NPs

BCMA72 − 80[YLMFLLRKI] peptide

MM

Increase peptide delivery to human dendritic cells, which enhance induction of BCMA-specific CTL

[169]

  1. APC Antigen-presenting cell, WT1 Wilms tumor protein 1, GM-CSF Granulocyte–macrophage colony-stimulating factor, LNT cells Liquid nitrogen-treated cells, DOX Doxorubicin, TLR Toll-like receptors, PLGA Poly(lactic-co-glycolic acid), BCMA B cell maturation antigen