Literature DB >> 16040383

Cost-effective manufacture of an allogeneic GM-CSF-secreting breast tumor vaccine in an academic cGMP facility.

J M Davis-Sproul1, M P Harris, N E Davidson, B J Kobrin, E M Jaffee, L A Emens.   

Abstract

BACKGROUND: GM-CSF-secreting, allogeneic cell-based cancer vaccines have shown promise for the treatment of a variety of solid tumors. We have now applied this approach to breast cancer. The aim of these studies was to optimize expansion parameters, qualify the manufacturing process, and establish expected outcomes for cGMP-compliant manufacturing of two GM-CSF-secreting breast tumor cell lines.
METHODS: The variables affecting the efficiency of expanding and formulating two allogeneic GM-CSF-secreting cell lines, 2T47D-V and 3SKBR3-7, were systematically evaluated. Production criteria investigated included alternative cell culture vessels (flasks vs. cell factories), centrifugation time and speed variables for large volume cell concentration, cell seeding density, the minimal concentration of FBS required for maximal cell expansion, and the dose and timing of irradiation in relation to cryopreservation.
RESULTS: These studies demonstrate that, in comparison with standard 150-cm2 tissue culture flasks, Nunc 10-Stack Cell Factories are a more efficient and practical cell culture vessel for vaccine cell line manufacture. Centrifugation optimization studies using the COBE 2991 Cell Processor established that a speed of 2000 r.p.m. (450 g) for 2 min reliably concentrated the cells while maintaining acceptable viability and bioactivity. Radiation studies established that lethal irradiation prior to cryopreservation does not compromise the quality of the product, as measured by post-thaw cell viability and GM-CSF cell line-specific secretion levels. Finally, studies aimed at optimizing the production of one vaccine cell line, 3SKBR3-7, demonstrated that seeding the cells at a higher density and maintaining them in half the initial concentration of FBS maximized the yield of bioactive cells, resulting in significant cost savings. DISCUSSION: A manufacturing process that simultaneously maximizes cell yield, minimizes cell manipulation and maintains vaccine cell potency is critical for producing cell-based cancer vaccines in an academic setting. These studies define a feasible, reproducible and cost-effective methodology for production of a GM-CSF-secreting breast cancer vaccine that is cGMP compliant.

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Year:  2005        PMID: 16040383     DOI: 10.1080/14653240510018082

Source DB:  PubMed          Journal:  Cytotherapy        ISSN: 1465-3249            Impact factor:   5.414


  6 in total

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Authors:  Gang Chen; Richa Gupta; Silvia Petrik; Marina Laiko; James M Leatherman; Justin M Asquith; Maithili M Daphtary; Elizabeth Garrett-Mayer; Nancy E Davidson; Kellie Hirt; Maureen Berg; Jennifer N Uram; Tianna Dauses; John Fetting; Elizabeth M Duus; Saadet Atay-Rosenthal; Xiaobu Ye; Antonio C Wolff; Vered Stearns; Elizabeth M Jaffee; Leisha A Emens
Journal:  Cancer Immunol Res       Date:  2014-08-12       Impact factor: 11.151

Review 2.  Re-purposing cancer therapeutics for breast cancer immunotherapy.

Authors:  Leisha A Emens
Journal:  Cancer Immunol Immunother       Date:  2012-03-28       Impact factor: 6.968

3.  Immunotherapy for Breast Cancer: What Are We Missing?

Authors:  Robert H Vonderheide; Susan M Domchek; Amy S Clark
Journal:  Clin Cancer Res       Date:  2017-06-01       Impact factor: 12.531

4.  Timed sequential treatment with cyclophosphamide, doxorubicin, and an allogeneic granulocyte-macrophage colony-stimulating factor-secreting breast tumor vaccine: a chemotherapy dose-ranging factorial study of safety and immune activation.

Authors:  Leisha A Emens; Justin M Asquith; James M Leatherman; Barry J Kobrin; Silvia Petrik; Marina Laiko; Joy Levi; Maithili M Daphtary; Barbara Biedrzycki; Antonio C Wolff; Vered Stearns; Mary L Disis; Xiaobu Ye; Steven Piantadosi; John H Fetting; Nancy E Davidson; Elizabeth M Jaffee
Journal:  J Clin Oncol       Date:  2009-10-05       Impact factor: 44.544

Review 5.  Potential clinical applications of adult human mesenchymal stem cell (Prochymal®) therapy.

Authors:  Amit N Patel; Jorge Genovese
Journal:  Stem Cells Cloning       Date:  2011-11-17

6.  Regulation gene expression of miR200c and ZEB1 positively enhances effect of tumor vaccine B16F10/GPI-IL-21 on inhibition of melanoma growth and metastasis.

Authors:  Xiaoying Wang; Xiangfeng He; Fengshu Zhao; Jing Wang; Hongyi Zhang; Fangfang Shi; Yunxia Zhang; Kai Cai; Jun Dou
Journal:  J Transl Med       Date:  2014-03-14       Impact factor: 5.531

  6 in total

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