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Gene transfer of human TCR in primary murine T cells is improved by pseudo‐typing with amphotropic and ecotropic envelopes
Author(s) -
Pouw Nadine M. C.,
Westerlaken Elike J.,
Willemsen Ralph A.,
Debets Reno
Publication year - 2007
Publication title -
the journal of gene medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.689
H-Index - 91
eISSN - 1521-2254
pISSN - 1099-498X
DOI - 10.1002/jgm.1047
Subject(s) - transduction (biophysics) , t cell receptor , biology , microbiology and biotechnology , t cell , antigen , virology , transfection , streptamer , cytotoxic t cell , transgene , murine leukemia virus , cell culture , gene , virus , in vitro , immune system , immunology , genetics , biochemistry
Background T cell receptor (TCR) gene therapy represents an attractive anti‐cancer treatment but requires further optimization of its efficacy and safety in clinically relevant models, such as those using a tumor antigen and TCR of human origin. Currently, however, there is no consensus as to what protocol is most optimal for retroviral human TCR gene transfer into primary murine T cells, most notably with respect to virus pseudo‐type. Methods Primary murine T cells were transduced, expanded and subsequently tested for transgene expression, proliferation and antigen‐specific function. To this end, murine leukemia virus (MLV) retroviruses were produced upon transfection of various packaging cells with genes encoding either green fluorescent protein (GFP) or TCRαβ specific for human melanoma antigen gp100 280–288 and the helper elements GAG/POL and ENV. Next to viral pseudotyping, the following parameters were studied: T cell densities; T cell activation; the amounts of IL‐2 and the source of serum used to supplement medium. Results The pseudo‐type of virus produced by packaging cells critically determines T cell transduction efficiencies. In fact, MLV‐A and MLV‐E pseudo‐typed viruses derived from a co‐culture of Phoenix‐A and 293T cells resulted in T cell transduction efficiencies that were two‐fold higher than those based on retroviruses expressing either VSV‐G, GALV, MLV‐A or MLV‐E envelopes. In addition, T cell densities during transduction were inversely related to transduction efficiencies. Further optimization resulted in transduction efficiencies of over 90% for GFP, and 68% for both a murine and a human (i.e. murinized) TCR. Importantly, TCR‐transduced T cells proliferate (i.e. showing a log increase in cell number in a few days) and show antigen‐specific function. Conclusions We set up a quick and versatile method to genetically modify primary murine T cells based on transient production of TCR‐positive retroviruses, and show that retroviral gene transfer of a human TCR into primary murine T cells is critically improved by viral pseudo‐typing with both MLV‐A and MLV‐E envelopes. Copyright © 2007 John Wiley & Sons, Ltd.