A chimeric switch receptor for macrophages and its application

By constructing a chimeric switch receptor and combining it with lipid nanoparticles and a hydrogel-liposome system, the transformation of M2 macrophages to M1 was achieved, solving the problems of high cost and side effects in the treatment of renal cancer and achieving precise drug delivery and anti-tumor effects in local targeted tumor therapy.

CN119409837BActive Publication Date: 2025-09-19LIFE VALLEY (QINGDAO) HEALTH TECHNOLOGY CO LTD
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Patent Information

Application Number
CN202411543869.0
Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
Filing Date
2024-10-31
Publication Date
2025-09-19
Estimated Expiration
2044-10-31

AI Technical Summary

Technical Problem

Existing treatments for kidney cancer have problems such as high cost, severe side effects, and easy development of drug resistance. In addition, immunotherapy is not effective, especially for patients with advanced kidney cancer. There is a lack of effective new treatment strategies and drugs.

Method used

A chimeric switch receptor is constructed, including the extracellular domain of IL-2α, IL-2β or IL-2γ receptor, the transmembrane domain of CD8 or CD28 and the intracellular domain of CD3ζ, TLR4, CD40 or Dectin1. Through lipid nanoparticle delivery system and hydrogel-liposome combined drug delivery system, the conversion of M2 macrophages to M1 type is achieved for local targeted tumor treatment.

Benefits of technology

It achieves the phagocytic killing effect of tumor cells, reduces toxic side effects, realizes precise drug delivery and anti-tumor effects for renal cancer, and avoids adverse reactions caused by systemic medication.

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Abstract

The present invention discloses a chimeric switch receptor for macrophages and its application, which belongs to the field of biomedicine technology. The chimeric switch receptor for macrophages provided by the present invention includes: an extracellular region, the extracellular region includes the extracellular domain of IL-2α, IL-2β or IL-2γ receptor; a transmembrane region, the transmembrane region includes the transmembrane domain of CD8 or CD28 molecule; an intracellular region, the intracellular region includes the intracellular domain of CD3ζ, TLR4, CD40 or Dectin1 molecule. The chimeric switch receptor of the present invention is expressed on the surface of tumor-associated macrophages, which can induce M2 macrophages to transform towards M1 phenotype after binding of exogenous IL-2 to the chimeric switch receptor on the cell surface, thereby fully exerting the phagocytic and killing effect on tumor cells.
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