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  4. Biomimetic and Materials-Potentiated Cell Engineering for Cancer Immunotherapy

Biomimetic and Materials-Potentiated Cell Engineering for Cancer Immunotherapy

Pharmaceutics, 2022 · DOI: 10.3390/pharmaceutics14040734 · Published: March 29, 2022

OncologyRegenerative MedicineBiomedical

Simple Explanation

In cancer immunotherapy, immune cells are the main force for tumor eradication. However, they appear to be dysfunctional due to the taming of the tumor immunosuppressive microenvironment. Recently, many materials-engineered strategies are proposed to enhance the anti-tumor effect of immune cells. These strategies either utilize biomimetic materials, as building blocks to construct inanimate entities whose functions are similar to natural living cells, or engineer immune cells with functional materials, to potentiate their anti-tumor effects. Biomimetic strategies utilize bioactive cell-derived components or biomimetic materials, as building blocks to construct inanimate entities whose functions are similar to natural living cells (Table 1). The abilities of targeting [10,11], chemotaxis [12], invisibility [13], antigen presentation [14], phagocytosis and killing can be achieved via cell-mimicking strategies [15,16].

Study Duration
Not specified
Participants
Not specified
Evidence Level
Review

Key Findings

  • 1
    Materials-potentiated cell engineering strategies are to endow immune cells with different supportive components (also known as backpack strategies), or functional materials to enhance their anti-tumor effects, prevent and rescue their dysfunction, maintain and restore their anti-tumor phenotype
  • 2
    T cell mimics could be fabricated as decoys to ameliorate immunosuppression and prevent excessive immune responses. Taking advantage of biomimetic materials, multiple immunosuppressive signals can be blocked.
  • 3
    The dual aptamer-modified T-P-NK cells showed higher affinity to HepG2 cells and secreted more IFN-γ. The tumor cell apoptosis rate rose with the increase in the effector-to-target (E/T) ratio, and significantly exceeded other groups.

Research Summary

With the deep understanding of the effector mechanisms of immune cells, the biomimetic and materials-potentiated cell engineering is refreshing its meaning. The combination of cell or cell-derived components with materials combines the sensitivity and specificity of naturally occurring interactions and the maneuverability of materials, to achieve specific therapeutic effects. Use or simulate cell-derived components (e.g., intracellular proteins, death ligand, or key signals) to enhance the anti-tumor effect of biomimetic cells. Blockade the signals that are inhibiting the recognition (e.g., PD-1/PD-L1 pathway), phagocytosis (e.g., CD47-SIRPα pathway) or the killing of tumor cells (e.g., adenosine and IDO) of immune cells. Despite the rapid progress, there are still some challenges for biomimetic strategies to simulate immune functions of immune cells. Although the cell analogs obtained by biomimetic materials have rich functions and strong maneuverability, they are nonliving and do not have the ability to proliferate.

Practical Implications

Enhanced Anti-tumor Effects

Biomimetic and materials-potentiated cell engineering can enhance the anti-tumor effects of immune cells by mimicking or improving their natural functions.

Targeted Immunotherapy

These strategies allow for more targeted immunotherapy by delivering drugs and therapeutic molecules directly to immune cells and tumor sites.

Overcoming Immune Suppression

The strategies help overcome the immunosuppressive tumor microenvironment, enabling immune cells to maintain their anti-tumor phenotype and function effectively.

Study Limitations

  • 1
    Nonliving nature of biomimetic cells limits proliferation
  • 2
    Combination rules for different materials and components are not clear
  • 3
    Long-term toxicity and drug release kinetics require further study

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