Preferential generation of monoclonal IgG-producing hybridomas by use of vesicular stomatitis virus-mediated cell fusion.

Vesicular stomatitis virus (VSV)-mediated cell fusion was recently proposed as an alternative fusion technique to generate monoclonal antibody (MAb)-producing hybridomas. In order to further examine this technique, we made direct comparative experiments among VSV, Sendai virus (SV) and polyethylene glycol (PEG)-mediated cell fusion in generating MAb-producing hybridomas. The distribution of immunoglobulin (Ig) isotypes secreted by the hybridomas obtained, as well as hybridoma yield and specific hybridoma yield, was compared. The results show that VSV-fusion yielded almost the same number of specific hybridomas as SV- and PEG-fusion in spite of its lower fusion frequency. In addition, VSV-fusion preferentially gave Ig-producing, especially IgG-producing, hybridomas. SV-fusion yielded both hybridomas and specific hybridomas with similar frequency to PEG-fusion, but IgM-producers predominated. These results demonstrate that fusion method has a considerable influence on the isotypes of obtained antibodies, and also suggest an advantage of VSV-fusion for production of IgG monoclonal antibodies.

[1]  U. Karsten,et al.  Direct comparison of electric field-mediated and PEG-mediated cell fusion for the generation of antibody producing hybridomas. , 1988, Hybridoma.

[2]  A. Macario,et al.  Hybridoma technology: new developments of practical interest , 1987, Journal of Immunological Methods.

[3]  T. Tokunaga,et al.  Improvement in the basic technology of electrofusion for generation of antibody-producing hybridomas. , 1987, Journal of immunological methods.

[4]  D. Wojchowski,et al.  Hybridoma production by simplified avidin-mediated electrofusion. , 1986, Journal of immunological methods.

[5]  R. Lane,et al.  A short-duration polyethylene glycol fusion technique for increasing production of monoclonal antibody-secreting hybridomas. , 1985, Journal of immunological methods.

[6]  U. Zimmermann,et al.  An improved electrofusion technique for production of mouse hybridoma cells , 1985, FEBS letters.

[7]  A. Naipal,et al.  Improved fusion technique. II. Stability and purity of hybrid clones. , 1984, Journal of immunological methods.

[8]  D. Scheidegger,et al.  Production of monoclonal antibodies: strategy and tactics. , 1980, Journal of immunological methods.

[9]  G. Köhler,et al.  A better cell line for making hybridomas secreting specific antibodies , 1978, Nature.

[10]  K. Rajewsky,et al.  Analysis of the repertoire of anti‐NP antibodies in C57BL/6 mice by cell fusion. I. Characterization of antibody families in the primary and hyperimmune response , 1978, European journal of immunology.

[11]  C. Milstein,et al.  Derivation of specific antibody‐producing tissue culture and tumor lines by cell fusion , 1976, European journal of immunology.

[12]  S. Snyder,et al.  Monoclonal antibody production by receptor-mediated electrically induced cell fusion , 1984, Nature.

[13]  S. Knutton The mechanism of virus-induced cell fusion , 1978 .