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Priming to Mycobacterial Antigen In Vivo Using Antigen-Pulsed Antigen Presenting Cells Generated In Vitro is Influenced by the Dose and Presence of IL-4 in APC Cultures
Authors:S. M. DILLON,D. N. J. HART,N. ABERNETHY,J. D. WATSON,&   M. A. BAIRD
Affiliation:Department of Pathology, Dunedin School of Medicine, University of Otago, New Zealand,;Department of Pathology, Christchurch School of Medicine, University of Otago, New Zealand,;Genesis Research and Development Corporation Ltd, Auckland, New Zealand
Abstract:
Antigen presenting cells (APC) similar to immature dendritic cells can be generated in vitro from bone marrow precursors. The authors have compared the yield, the phenotype and the function of murine bone marrow cells cultured for 7 or 11 days in either granulocyte macrophage colony stimulating factor alone (GM BMAPC) or in combination with interleukin-4 (GM/IL-4 BMAPC). The results showed that GM/IL-4 BMAPC expressed the highest levels of MHC Class 2 molecules, CD86 /B7-2 and CD80/B7-1 co-stimulatory molecules and the lowest levels of F4/80 macrophage marker. However, when these APC were pulsed with BCG culture filtrate antigen or PPD they were not correspondingly more effective at stimulating activated T lymphocytes in vitro or priming naive T lymphocytes in vivo . Also, in contrast to GM BMAPC, high backgrounds recorded following injections of GM/IL-4 BMAPC without antigen were not consistently reduced by lowering the dose and irradiating the cells prior to administration. The authors conclude that the degree of maturity of BMAPC varies with culture conditions and that this may be an important consideration where BMAPC are to be used in vivo in immunotherapeutic regimens.
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