Open AccessHuman T cells in hu‐PBL‐SCID mice proliferate in response to Daudi lymphoma and confer anti‐tumour immunity
Author(s) -
MALKOVSKA V.,
CIGEL F.,
STORER B. E.
Publication year - 1994
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/j.1365-2249.1994.tb06246.x
Subject(s) - immunology , severe combined immunodeficiency , cytotoxic t cell , lymphoma , cd3 , antigen , adoptive cell transfer , cytotoxicity , microbiology and biotechnology , medicine , population , t cell , biology , immune system , in vitro , cd8 , in vivo , biochemistry , environmental health
SUMMARY In vitro culture of human peripheral blood lymphocytes (PBL) with Daudi (Burkitt lymphoma) cells results in selective proliferation of Vγ9/Vδ2 T cells with high cytotoxicity against Daudi cells. After adoptive transfer into severe combined immunodeficient (SCID) mice, these cells exert specific anti‐tumour activity against Daudi lymphoma. To test whether cytotoxic Vγ9/Vδ2 T cells are induced in SCID mice, human PBL injected intraperitoneally were stimulated with irradiated Daudi cells (PBL/ Daudi‐SCID). After 7–14 days, PBL/Daudi‐SCID had a significantly higher percentage of human γδ T cells in their peritoneal cavity, lymph nodes and blood than controls (PBL‐SCID). DNA content analysis of T cell subsets from PBL/Daudi‐SCID showed a significantly higher percentage of cells in S + G 2 +M phases of the cell cycle in the TCR‐γδ‐1 + than in CD3 + cell population. Human cells recovered from PBL/Daudi‐SCID showed specific cytotoxicity against Daudi cells. PBL/Daudi‐SCID inoculated with a lethal dose of Daudi lymphoma survived significantly longer than controls. This protection was specific for Daudi cells and was not mediated by murine natural killer (NK) cells. Thus human peripheral blood T cells grafted in SCID mice proliferate in response to antigen and confer specific immunity.