Effects of interleukin-12 on in vitro culture with interleukin-2 of regional lymph node lymphocytes from lung cancer patients

Springer Science and Business Media LLC - Tập 43 - Trang 87-93 - 1996
T. Hanagiri1, Mitsuhiro Takenoyama2, Takashi Yoshimatsu1, Chikashi Hirashima2, Ichiro Yoshino1, Kozo Nakanishi1, Akira Nagashima3, Kikuo Nomoto2, Kosei Yasumoto1
1The Department of Surgery II, School of Medicine, University of Occupational and Environmental Health, Yahatanishi, Kitakyushu 807, Japan Fax: (93)-692-4004, , JP
2The Department of Immunology, Medical Institute of Bioregulation, Kyushu University,
3The Department of Chest Surgery, Kitakyushu Municipal Medical Center,

Tóm tắt

 In the present study, we carried out a functional analysis of regional lymph node lymphocytes (RLNL) from patients with lung cancer after in vitro activation by interleukin-2 (IL-2) and interleukin-12 (IL-12). IL-12 (100 U/ml) enhanced both the proliferation and cytotoxic activity of RLNL in a culture with low doses of IL-2 (5 – 10 JRU/ml). After comparing an RLNL culture with a low dose of IL-2 alone, a higher proportion of CD8+ cells and CD56+ cells and a lower proportion of CD4+ cells were found in the culture with both IL-12 and a low dose of IL-2. Such a combination of the cytokines effectively activated RLNL in terms of the expression of IL-2 receptors. In the culture condition of IL-12 and a low dose of IL-2, a synergistic effect was observed in the production of such cytokines as interferon γ, tumor necrosis factor α (TNFα), and TNFβ, as well as in tumor cytotoxicity. However, the addition of IL-12 inhibited the cytotoxicity of RLNL in the culture with a high dose of IL-2 (100 JRU/ml). This inhibition is considered to be partially due to the endogenous production of TNFα by lymphocytes, because the neutralization of TNFα bioactivity partially restored the cytotoxic activities of RLNL. Furthermore, in the presence of hydrocortisone, IL-12 synergistically enhanced the cytotoxic activity of RLNL cultured with a high dose of IL-2. These results provide useful information about the improvement of adoptive immunotherapy against cancer using RLNL.