Human T cell hybrids were generated by fusing lectin-activated normal and leukemic human T cells with an aminopterin-sensitive human T cell line. This mutant cell line, designated CEM-T15, was derived from the human T cell line CEM after chemical mutagenesis with ethane methylsulfonate and subsequent culture in medium containing 6-thioguanine. After polyethylene glycol-induced fusion, the cells were cultured in hypoxanthine-aminopterin-thymidine selective medium. More than 5 wk after fusion, evidence for successful hybridization was obtained by three independent criteria: (a) The majority of the cultures contained cells expressing the OKT3 surface antigen: this antigen is expressed on normal T cells but not on CEM-T15 cells. (b) Most of the cultures contained polyploid cells. (c) Some of the cultures provided helper activity in the generation of antibody-forming cells. This functional activity is absent from the CEM-T15 parental cell line. Evidence for functional stability of the hybrids greater than 20 wk after fusion was provided by several clones that not only continue growing exponentially but also maintain expression of OKT3 surface antigen and high levels of helper function. These T cell hybrids constructed using antigen-specific human T cells should be of considerable importance in further studies of the immunobiology of human T cells.
Article| December 01 1981
Generation of functional human T cell hybrids.
P V Rizzolo
Online Issn: 1540-9538
Print Issn: 0022-1007
J Exp Med (1981) 154 (6): 1827–1837.
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O Irigoyen, P V Rizzolo, Y Thomas, L Rogozinski, L Chess; Generation of functional human T cell hybrids.. J Exp Med 1 December 1981; 154 (6): 1827–1837. doi: https://doi.org/10.1084/jem.154.6.1827
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