Article citationsMore>>
I. Airoldi, E. Di Carlo, C. Cocco, E. Caci, M. Cilli, C. Sorrentino, G. Sozzi, S. Ferrini, S. Rosini, G. Bertolini, M. Truini, F. Grossi, L. J. Galietta, D. Ribatti and V. Pistoia, “IL-12 Can Target Human Lung Adenocarcinoma Cells and Normal Bronchial Epithelial Cells Surrounding Tumor Lesions,” PLoS One, Vol. 4, No. 7, 2009, Article ID: e6119. doi:10.1371/journal.pone.0006119
has been cited by the following article:
-
TITLE:
Low Dose of IL-12 Stimulates T Cell Response in Cultures of PBMCs Derived from Non Small Cell Lung Cancer Patients
AUTHORS:
Lucia D’Amico, Enrico Ruffini, Riccardo Ferracini, Ilaria Roato
KEYWORDS:
Interleukin-12; Immuno-Modulation; T Helper; T Regulatory; Anti-Tumor Immune Response
JOURNAL NAME:
Journal of Cancer Therapy,
Vol.3 No.4A,
September
12,
2012
ABSTRACT: Cancer induces tolerance by suppressing immune function, modulating the T helper activity and causing an imbalance of cytokines produced by T cells. IL-12 is an immune regulatory cytokine with potent anti-tumor activity and its signalling network leads to polarization of na?ve CD4+ T cells into Th1. In pre-clinical studies, administration of recombinant IL-12 by intravenous injection or IL-12 plasmid DNA by intra-tumoral injection showed some anti-tumor effects, measurable immunological responses, but also important dose-dependent side effects. We investigated the ability of low doses of IL-12 to modulate the T cell subpopulations in cultures of PBMCs derived from Non Small Lung Cancer (NSCLC) patients and to induce lysis of lung adenocarcinoma cells by T cells. PBMCs were stimulated with different doses of IL-12 and T cell phenotype was evaluated. IL-12 at 0.01 pg/ml significantly increased the number of CD4 and CD8 T cells, in particular of CD4/IFNγ producing cells. IL-12 did not stimulate T regulatory, but it increased the lysis of lung adenocarcinoma cells induced by T cells. Our results showed that low doses of IL-12 modulates T cell sub-populations in vitro and it increased their lytic activity on adenocarcinoma cells, thus we hypothesize the use of low dose of IL-12 as a therapeutic tool against pathologies characterized by a T cell imbalance, in order to promote an immuno-modulation.