Original research

A new approach for the large-scale generation of mature dendritic cells from adherent PBMC using roller bottle technology

Ryan E Campbell-Anson¹ , Diane Kentor¹ , Yi J Wang¹ , Kathryn M Bushnell¹ , Yufeng Li¹ , Luis M Vence¹ and Laszlo G Radvanyi^1,2

¹Department of Melanoma Medical Oncology, University of Texas, M.D. Anderson Cancer Center, Houston, TX, 77030, USA

²Department of Breast Medical Oncology, University of Texas, M.D. Anderson Cancer Center, Houston, TX, 77030, USA

author email corresponding author email

Journal of Immune Based Therapies and Vaccines 2008, 6:1doi:10.1186/1476-8518-6-1

Published:	6 March 2008

Abstract

Background

Human monocyte-derived DC (mDC) loaded with peptides, protein, tumor cell lysates, or tumor cell RNA, are being tested as vaccines against multiple human malignancies and viral infection with great promise. One of the factors that has limited more widespread use of these vaccines is the need to generate mDC in large scale. Current methods for the large-scale cultivation of mDC in static culture vessels are labor- and time- intensive, and also require many culture vessels. Here, we describe a new method for the large-scale generation of human mDC from human PBMC from leukopheresis or buffy coat products using roller bottles, never attempted before for mDC generation. We have tested this technology using 850 cm² roller bottles compared to conventional T-175 flat-bottom static culture flasks.

Methods

DC were generated from adherent human PBMC from buffy coats or leukopherisis products using GM-CSF and IL-4 in T-175 static flasks or 850 cm² roller bottles. The cells were matured over two days, harvested and analyzed for cell yield and mature DC phenotype by flow cytometry, and then functionally analyzed for their ability to activate allogeneic T-cell or recall antigen peptide-specific T-cell responses.

Results

Monocytes were found to adhere inside roller bottles to the same extent as in static culture flasks. The phenotype and function of the mDC harvested after maturation from both type of culture systems were similar. The yield of mDC from input PBMC in the roller bottle system was similar as in the static flask system. However, each 850 cm² roller bottle could be seeded with 4–5 times more input PBMC and could yield 4–5 times as many mDC per culture vessel than the static flasks as a result.

Conclusion

Our results indicate that the roller bottle technology can generate similar numbers of mDC from adherent PBMC as traditional static flask methods, but with having to use fewer culture vessels. Thus, this may be a more practical method to generate mDC in large-scale cutting down on the amount of laboratory manipulations, and can save both time and labor costs.