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Preclinical Toxicity Evaluation of Chimeric Antigen Receptor T Cells U87 Targeting at Pancreatic Cancer in Tumor Bearing Mice
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Hairuo WEN1, Guitao HUO1, Chao QIN1, Jing ZHAO1, Xiaoxuan KOU1, Xiaoyan LOU2, Xiaobing ZHOU1, *, Ying HUANG1, *, Lei YU2
Chinese Pharmaceutical Journal | 2024, 59(20) : 1889 - 1898
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Chinese Pharmaceutical Journal | 2024, 59(20): 1889-1898
Preclinical Toxicity Evaluation of Chimeric Antigen Receptor T Cells U87 Targeting at Pancreatic Cancer in Tumor Bearing Mice
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Hairuo WEN1, Guitao HUO1, Chao QIN1, Jing ZHAO1, Xiaoxuan KOU1, Xiaoyan LOU2, Xiaobing ZHOU1, *, Ying HUANG1, *, Lei YU2
Affiliations
  • 1 Key Laboratory of Beijing for Nonclinical Safety Evaluation Research of Drugs, National Center for Safety Evaluation of Drugs, National Institutes for Food and Drug Control, Beijing 100176, China
  • 2 Shanghai Unicar Therapy Biomedicine Technology Co., Ltd., Shanghai 201203, China
Published: 2024-10-22 doi: 10.11669/cpj.2024.20.002
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OBJECTIVE To evaluate the preclinical safety of chimeric antigen receptor T (CAR-T) cell U87 in tumor-bearing immunodeficient mice. METHODS A transplantation tumor model was constructed using NCG mice subcutaneously inoculated with BxPC-3, on which cells U87 (2×106cells each mouse and 10×106 cells each mouse) were administered in a single dose, and continued to be observed until day 84 after administration. Tumor clearance, survival rate, clinical symptoms, body weight changes, hematological indices, lymphocyte subpopulation classification, cytokine indices, and histopathological changes were examined to characterize the mice. RESULTS Single tail vein administration of U87 to hormonal NCG mice significantly prolonged mouse survival and even completely cleared the tumor load. As its pharmacodynamic action, U87 resulted in elevated levels of human-derived IFN-γ, as well as mixed cell aggregation in multiple tissues/organisms, with no local irritation and no apparent systemic toxicity associated with U87. U87 led excessive immune response at high doses, and has certain effects on the values of GLU, TG, TP, ALB, PLT and RET in animals. Mild GvHD-associated histopathological changes were only observed in 2×106 CAR-T (from week 8 after cell administration) and 10×106 CAR-T (from week 4 after cell administration), and the changes correlated with the level of T-cell proliferation. No tumor formation associated with U87 was seen. CONCLUSION U87 does not show any significant risk associated with immunotoxicity and tumorigenicity in BxPC-3 loaded NCG mice and shows some pharmacodynamic effects. The results of this study provide implications for the toxicological evaluation of targeted solid tumors.

chimeric antigen receptor T cell  /  pancreatic cancer  /  immunodeficient tumor-bearing mice  /  solid tumor  /  toxicity evaluation
Hairuo WEN, Guitao HUO, Chao QIN, Jing ZHAO, Xiaoxuan KOU, Xiaoyan LOU, Xiaobing ZHOU, Ying HUANG, Lei YU. Preclinical Toxicity Evaluation of Chimeric Antigen Receptor T Cells U87 Targeting at Pancreatic Cancer in Tumor Bearing Mice[J]. Chinese Pharmaceutical Journal, 2024 , 59 (20) : 1889 -1898 . DOI: 10.11669/cpj.2024.20.002
Year 2024 volume 59 Issue 20
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doi: 10.11669/cpj.2024.20.002
  • Receive Date:2024-06-26
  • Online Date:2025-12-30
  • Published:2024-10-22
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  • Received:2024-06-26
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    1 Key Laboratory of Beijing for Nonclinical Safety Evaluation Research of Drugs, National Center for Safety Evaluation of Drugs, National Institutes for Food and Drug Control, Beijing 100176, China
    2 Shanghai Unicar Therapy Biomedicine Technology Co., Ltd., Shanghai 201203, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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