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Natural Killer Cell Activity of Human Fetal Liver Cells after Allogeneic Stimulation
Author(s) -
UKSILA J.,
LASSILA O.,
HIRVONEN T.,
TOIVANEN P.
Publication year - 1985
Publication title -
scandinavian journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.934
H-Index - 88
eISSN - 1365-3083
pISSN - 0300-9475
DOI - 10.1111/j.1365-3083.1985.tb01901.x
Subject(s) - cytotoxic t cell , fetus , k562 cells , lymphokine activated killer cell , biology , immunology , cell culture , interleukin 12 , andrology , medicine , in vitro , leukemia , biochemistry , pregnancy , genetics
Cells isolated from the liver of human fetuses were confronted with mitomycin C‐treated adult allogeneic cells. After this mixed leukocyte culture (MLC)‐type reaction, the cytotoxic activity of fetal cells was tested against K562 cell line in a 4‐h 51 Cr release assay. Three of the seven fetuses tested (8 to 11 weeks of gestational age) expressed marginal cytotoxic activity before cultivation. Cells from one 8‐week‐old and one 9‐week‐old fetus were slightly more cytotoxic when cultured in the presence of allogeneic cells than when cultured in the medium only. Production of gamma interferon (IFN‐γ) was not detected in these cultures. Cells of one 18‐week‐old fetus expressed strong cytotoxic activity against K562 cells after MLC. Thymocytes from the same fetus were not cytotoxic, either before or after MLC against K562 cells. The results indicate that the ‘prethymic’ human liver contains cytotoxic cells able to spontaneously kill natural killer (NK)‐sensitive target cells. Generation of strong NK‐like cytotoxicity from noncytotoxic precursor cells was observed only after the thymus becomes lymphoid, suggesting that thymus‐processed cells may regulate the generation of NK‐like cytotoxic activity. The results suggest a different ontogenity of spontaneous and MLC‐induced NK‐like cells in the human fetus.