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Generation and testing of clinical-grade exosomes for pancreatic cancer
Mayela Mendt, … , Valerie S. LeBleu, Raghu Kalluri
Mayela Mendt, … , Valerie S. LeBleu, Raghu Kalluri
Published April 19, 2018
Citation Information: JCI Insight. 2018;3(8):e99263. https://doi.org/10.1172/jci.insight.99263.
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Research Article Oncology

Generation and testing of clinical-grade exosomes for pancreatic cancer

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Abstract

Exosomes are extracellular vesicles produced by all cells with a remarkable ability to efficiently transfer genetic material, including exogenously loaded siRNA, to cancer cells. Here, we report on a bioreactor-based, large-scale production of clinical-grade exosomes employing good manufacturing practice (GMP) standards. A standard operating procedure was established to generate engineered exosomes with the ability to target oncogenic Kras (iExosomes). The clinical-grade GMP iExosomes were tested in multiple in vitro and in vivo studies to confirm suppression of oncogenic Kras and an increase in the survival of several mouse models with pancreatic cancer. We perform studies to determine the shelf life, biodistribution, toxicology profile, and efficacy in combination with chemotherapy to inform future clinical testing of GMP iExosomes. Collectively, this report illustrates the process and feasibility of generating clinical-grade exosomes for various therapies of human diseases.

Authors

Mayela Mendt, Sushrut Kamerkar, Hikaru Sugimoto, Kathleen M. McAndrews, Chia-Chin Wu, Mihai Gagea, Sujuan Yang, Elena V. Rodriges Blanko, Qian Peng, Xiaoyan Ma, Joseph R. Marszalek, Anirban Maitra, Cassian Yee, Katayoun Rezvani, Elizabeth Shpall, Valerie S. LeBleu, Raghu Kalluri

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Figure 2

Exosome production by MSCs.

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Exosome production by MSCs.
(A) Representative bright-field images of BJ...
(A) Representative bright-field images of BJ fibroblasts and MSCs. Scale bar: 100 μm. (B) Comparison of the number of exosomes quantified by NanoSight, produced by the same number of BJ fibroblasts and MSCs, and collected from the conditioned media over a period of 48 hours (n = 3 independent collections). (C) Particle size distribution analysis of BJ fibroblast exosomes and MSC exosomes by NanoSight. (D and E) Representative histogram of flow cytometry analysis of exosomal markers (CD9, CD63, CD81), CD47, and mesenchymal markers (CD29, CD90) on BJ fibroblasts (red, D) exosomes and MSC exosomes (blue, E). Numbers represent the percentage of positive beads (gray, isotype control). The data are presented as the mean ± SEM. Unpaired 2-tailed t test was used to determine statistical significance. **P < 0.01. See Supplemental Source Data 1 and 2.

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