Open AccessINDUCTION OF NATURAL SUPPRESSOR-LIKE CELLS FROM HUMAN ADULT PERIPHERAL BLOOD LYMPHOCYTES BY A K562-DERIVED FACTOR
Author(s) -
Keisuke Hayamizu,
Hiroshi Yahata,
Yoshihiro Fukuda,
Kiyohiko Dohi
Publication year - 1993
Publication title -
transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.45
H-Index - 204
eISSN - 1534-6080
pISSN - 0041-1337
DOI - 10.1097/00007890-199306000-00036
Subject(s) - myeloid derived suppressor cell , k562 cells , biology , peripheral blood mononuclear cell , suppressor , microbiology and biotechnology , immunology , cd8 , cd19 , in vitro , antigen , leukemia , biochemistry , gene
K562-AC1, a subclone of the human myeloid leukemia cell line K562, secreted an inhibitor of PHA-stimulated human T cell growth into the culture supernatant (K562sup). Kinetics and absorption assays in vitro revealed that the factor acts on PBMC during the very early growth phase. PBMC gained potent suppressor activity against autologous T cell growth after preculture with K562sup for 3 days in a dose-related manner. HLA class II negative and nylon wool-nonadherent subsets possessed higher suppressor potential than unfractionated PBMC. Treatment of K562sup-precultured PBMC with mAb followed by complement-lysing showed that the responsible suppressors belong to null cells expressing CD3-, CD4-, CD19-, CD14-, CD11b-, but partially CD2+. Exogenous IL-2 exhibited a synergistic effect on the activity of the suppressors committed by K562sup. However, K562sup inhibited IL-2-activated lymphocytes from generating anti-K562 cytolytic activity. Macrophages inhibited the induction of the suppressors, which was restored by adding indomethacin and/or IL-2. In conclusion, K562sup has the ability to induce efficient suppressor cells from human adult PBL, which belong to null cells without NK/lymphocyte-activated killer activity and are similar to natural suppressor cells.