Phenotypic and functional characteristics of tumor‐associated lymphocytes in patients with malignant ascites receiving intraperitoneal infusions of recombinant interleukin‐2 (ril‐2)
- 15 February 1989
- journal article
- research article
- Published by Wiley in International Journal of Cancer
- Vol. 43 (2) , 231-234
- https://doi.org/10.1002/ijc.2910430210
Abstract
In the course of a phase I trial, in which recombinant IL‐2 (riL‐2) was infused intraperitoneally (i.p.) in patients with peritoneal carcinomatosis, we evaluated the effect on “tumorassociated lymphocytes” (TAL) isolated from the ascitic fluid. No major changes in the percentages of cells expressing the CD3, CD4, CD8, Leu‐7, OKM1 and WT‐31 antigens were detected either in TAL or in peripheral blood lymphocytes (PBL) after 7 days of rlL‐2 infusion. In contrast the percentages of TAL (but not PBL) expressing surface IL‐2 receptor (Tac), or LAK‐1 antigen were sharply increased. Analysis of cytolytic functions showed a potentiation of the lytic activity against natural‐killer (NK) sensitive K562 target cells and the de novo appearance of lytic activity against fresh melanoma cells. In one patient IFN‐γ was detected in the ascitic fluid following rIL‐2 infusion. T‐cell clones derived from the patient were analyzed for the IFN‐γ production. While only approximately 40% of PB‐derived control clones produced medium to low amounts of IFN‐γ, all of the TAL‐derived clones produced medium to high amounts of the lymphokine.This publication has 15 references indexed in Scilit:
- A monoclonal antibody specific for a common determinant of the human T cell receptor gamma/delta directly activates CD3+WT31- lymphocytes to express their functional program(s).The Journal of Experimental Medicine, 1988
- Phenotypic and functional analysis of human CD3 + and CD3− clones with “lymphokine‐activated killer” (LAK) activity. Frequent occurrence of CD3 + LAK clones which produce interleukin‐2International Journal of Cancer, 1987
- A novel 120-kD surface antigen expressed by a subset of human lymphocytes. Evidence that lymphokine-activated killer cells express this molecule and use it in their effector function.The Journal of Experimental Medicine, 1987
- A Progress Report on the Treatment of 157 Patients with Advanced Cancer Using Lymphokine-Activated Killer Cells and Interleukin-2 or High-Dose Interleukin-2 AloneNew England Journal of Medicine, 1987
- Constant-Infusion Recombinant Interleukin-2 in Adoptive Immunotherapy of Advanced CancerNew England Journal of Medicine, 1987
- Separation, phenotyping and limiting dilution analysis of T‐lymphocytes infiltrating human solid tumorsInternational Journal of Cancer, 1986
- T cell nature of some lymphokine‐activated killer (LAK) cells. Frequency analysis of LAK precursors within human T cell populations and clonal analysis of LAK effector cellsEuropean Journal of Immunology, 1986
- Lymphokine-activated killer cell phenomenon. II. Precursor phenotype is serologically distinct from peripheral T lymphocytes, memory cytotoxic thymus-derived lymphocytes, and natural killer cellsThe Journal of Experimental Medicine, 1983
- Direct demonstration of the clonogenic potential of every human peripheral blood T cell. Clonal analysis of HLA-DR expression and cytolytic activity.The Journal of Experimental Medicine, 1983
- Lymphokine-activated killer cell phenomenon. Lysis of natural killer-resistant fresh solid tumor cells by interleukin 2-activated autologous human peripheral blood lymphocytes.The Journal of Experimental Medicine, 1982