Mitigation of Anti‐Drug Antibody Production for Augmenting Anticancer Efficacy of Therapeutic Protein via Co‐Injection of Nano‐Rapamycin

Author:

Chang Ya12,Xiong Wei234,Zou Chenming1,Zeng Ping1,Hou Jiazhen25,Muhitdinov Bahtiyor26,Shen Yuanyuan1,Huang Yongzhuo247ORCID,Guo Shengrong1

Affiliation:

1. School of Pharmacy Shanghai Jiao Tong University Shanghai 200240 China

2. State Key Laboratory of Drug Research Shanghai Institute of Materia Medica Chinese Academy of Sciences Shanghai 201203 China

3. Artemisinin Research Center Guangzhou University of Chinese Medicine Guangzhou 510450 China

4. Zhongshan Institute for Drug Discovery Shanghai Institute of Materia Medica Chinese Academy of Sciences Zhongshan 528437 China

5. School of Chinese Materia Medica Nanjing University of Chinese Medicine 138 Xianlin Avenue Nanjing 210023 China

6. Institute of Bioorganic Chemistry Uzbekistan Academy of Sciences Tashkent 100125 Uzbekistan

7. University of Chinese Academy of Sciences Beijing 100049 China

Abstract

AbstractThe induction of anti‐drug antibody (ADA) is a formidable challenge for protein‐based therapy. Trichosanthin (TCS) as a class of ribosome‐inactivating proteins is widely studied in tumor treatment. However, the immunogenicity can induce the formation of ADA, which can cause hypersensitivity reactions and neutralize the efficacy of TCS, thus limiting its clinical application in cancer therapy. Here, a promising solution to this issue is presented by co‐administration of the rapamycin nanoparticles and TCS. PEGylated rapamycin amphiphilic molecule is designed and synthesized as a prodrug and a delivery carrier, which can self‐assemble into a nanoparticle system with encapsulation of free rapamycin, a hydrophobic drug. It is found that co‐injection of the PEGylated rapamycin nanoparticles and TCS could mitigate the formation of anti‐TCS antibody via inducing durable immunological tolerance. Importantly, the combination of TCS and the rapamycin nanoparticles has an enhanced effect on inhibit the growth of breast cancer. This work provides a promising approach for protein toxin‐based anticancer therapy and for promoting the clinical translation.

Funder

National Key Research and Development Program of China

Guangdong Provincial Department of Science and Technology

National Outstanding Youth Science Fund Project of National Natural Science Foundation of China

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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