Spleen but not tumor infiltration by dendritic and T cells is increased by intravenous adenovirus-Flt3 ligand injection

Dendritic cell (DC) expansion is regulated by the hematopoietic growth factor fms-like tyrosine kinase 3 ligand (Flt3L). DCs are critical to the control of tumor growth and metastasis, and there is a positive correlation between intratumoral DC infiltration and clinical outcome. In this report, we f...

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Veröffentlicht in:Cancer gene therapy 2007-04, Vol.14 (4), p.364-371
Hauptverfasser: Solheim, J C, Reber, A J, Ashour, A E, Robinson, S, Futakuchi, M, Kurz, S G, Hood, K, Fields, R R, Shafer, L R, Cornell, D, Sutjipto, S, Zurawski, S, LaFace, D M, Singh, R K, Talmadge, J E
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Sprache:eng
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Zusammenfassung:Dendritic cell (DC) expansion is regulated by the hematopoietic growth factor fms-like tyrosine kinase 3 ligand (Flt3L). DCs are critical to the control of tumor growth and metastasis, and there is a positive correlation between intratumoral DC infiltration and clinical outcome. In this report, we first demonstrate that single intravenous (i.v.) injections of adenovirus (Adv)-Flt3L significantly increased splenic dendritic, B, T and natural killer (NK) cell numbers in both normal and mammary tumor-bearing mice. In contrast, the numbers of DCs and T cells infiltrating the tumors were not increased. Consistent with the minimal effect on immune cell infiltration, i.v. Adv-Flt3L injections had no therapeutic activity against orthotopic mammary tumors. In addition, we noted tumor and Adv-Flt3L expansion of Gr1 + CD11b + immature myeloid suppressor cells (IMSCs), which may inhibit the therapeutic efficacy of Adv-Flt3L-expanded DCs.
ISSN:0929-1903
1476-5500
DOI:10.1038/sj.cgt.7701018