Literature DB >> 16920502

Generation of dendritic cells for immunotherapy is minimally impaired by granulocytes in the monocyte preparation.

Anja ten Brinke1, Miriam L Karsten, Miranda C Dieker, Jaap Jan Zwaginga, Hans Vrielink, S Marieke van Ham.   

Abstract

The growing number of clinical studies, using monocyte-derived DC therapy, requires protocols where a sufficient number of dendritic cell (DCs) are produced according to current Good Manufacturing Practice guidelines. Therefore, a closed culture system for the generation of DCs is inevitable. One cost-effective way to isolate monocytes directly from leukapheresis material in a closed system is by elutriation with the Elutra cell separation system. In the Elutra, granulocytes co-purify with the monocytes. Therefore, we studied if and to what extent the presence of granulocytes in a monocyte product affects the generation of mature DCs. The presence of up to 16% granulocytes in the monocyte product had no significant effects on the quality of the DCs formed. The presence of higher granulocyte percentages, however, gradually altered DC quality. In this respect, the presence of higher number of granulocytes induced significant lower migratory capacity of the DCs and lower expression levels of CD80, CD40 and CD86. No effects were observed on the DC yield, cytokine production or the stimulatory capacity of the DCs in MLR. In conclusion, the presence of 20-30% granulocytes in a monocyte product has no major influence on the quality of the DCs generated from monocytes. Therefore, the Elutra is a suitable closed system apparatus to separate monocytes from other blood components for the generation of DCs, even from leukapheresis material which contains a high number of granulocytes.

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Year:  2006        PMID: 16920502     DOI: 10.1016/j.imbio.2006.05.012

Source DB:  PubMed          Journal:  Immunobiology        ISSN: 0171-2985            Impact factor:   3.144


  3 in total

1.  Generation of functionally mature dendritic cells from elutriated monocytes using polyinosinic : polycytidylic acid and soluble CD40 ligand for clinical application.

Authors:  S Kim; H O Kim; H J Kim; K Lee; H-S Kim
Journal:  Clin Exp Immunol       Date:  2008-09-08       Impact factor: 4.330

2.  Comparative evaluation of techniques for the manufacturing of dendritic cell-based cancer vaccines.

Authors:  Alexander Michael Dohnal; Sebastian Graffi; Volker Witt; Christina Eichstill; Dagmar Wagner; Sidrah Ul-Haq; Doris Wimmer; Thomas Felzmann
Journal:  J Cell Mol Med       Date:  2008-03-17       Impact factor: 5.310

3.  Counter-flow elutriation of clinical peripheral blood mononuclear cell concentrates for the production of dendritic and T cell therapies.

Authors:  David F Stroncek; Vicki Fellowes; Chauha Pham; Hanh Khuu; Daniel H Fowler; Lauren V Wood; Marianna Sabatino
Journal:  J Transl Med       Date:  2014-09-17       Impact factor: 5.531

  3 in total

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