Open AccessAugmentation by Tumor Necrosis Factor α of the Systemic Therapeutic Effect of Lymphokine‐activated Killer Cells in Adoptive Immunotherapy of Murine Tumor
Author(s) -
Kato Kazunori,
Tanabe Toshifumi,
Agatsuma Toshinori,
Suzuki Shinya,
Nitanai Hironobu,
Hashimoto Yoshiyuki
Publication year - 1991
Publication title -
japanese journal of cancer research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.035
H-Index - 141
eISSN - 1349-7006
pISSN - 0910-5050
DOI - 10.1111/j.1349-7006.1991.tb01871.x
Subject(s) - lymphokine activated killer cell , tumor necrosis factor alpha , immunotherapy , cancer research , lymphokine , medicine , interleukin 2 , immunology , adoptive cell transfer , cytokine , t cell , interleukin 21 , immune system
The therapeutic effect of a combined modality of lymphokine‐activated killer (LAK) cells and tumor necrosis factor α (TNFα) on MBL‐2 tumor in C57BL/6 mice was studied. Murine LAK cells induced from splenocytes by interleukin 2 (IL2) could lyse MBL‐2 target cells in vitro , but no enhancement of the LAK activity was found by the treatment of LAK cells with TNFα in vitro. However, the treatment of MBL‐2 with TNFα enhanced the sensitivity to LAK cells. Moreover, administration of TNFα to mice bearing solid MBL‐2 tumor led to increased tumor vascular permeability within 1 h, and resulted in the enhanced accumulation of systemically transferred LAK cells in tumor tissue. Based on these results, we treated MBL‐2‐bearing mice with TNFα and then with LAK cells 1 h later, No therapeutic effect was observed when tumor‐bearing mice were treated with TNFα alone or LAK cells plus IL2. However, adoptive immunotherapy using LAK cells and TNFα had therapeutic effects, i.e. growth inhibition of tumor nodules and prolongation of survival. These results indicated that appropriately timed pretreatment of tumor‐bearing mice with TNFα augmented the anti‐tumor efficacy of LAK cells.