Abstract
THE immune system is now recognised as a network of interacting cells with some interactions augmenting, and others suppressing immune responses. Regulatory interactions are often mediated by T cells, and do not always require cell-to-cell contact between appropriate cells, but may be mediated by soluble transmitters, commonly termed ‘factors’. Both antigen-specific1–7 and nonspecific8–10 factors have been described. Biochemical characterisation of these factors is hampered by the often minute quantities required to mediate biological effects and by the multiplicity of regulatory pathways involved in immune responses. Our knowledge of these factors is derived from functional tests, often combined with serological analysis of the factors. One approach to the analysis of monoclonal cell products is the somatic cell hybridisation technique described by Milstein et al.11,12. Using this method, specific antibody-forming cells have been hybridised with myeloma cells, and have yielded clones producing specific antibody11. This antibody is particularly useful as it is monoclonal and large quantities can be obtained. Although attempts to produce T-cell hybrids have been successful13–15, the products have not been functional. However, only failures in expression of cytotoxic activity have been described13–15. We describe here one antigen-specific suppressor factor (SF)-producing line S1-41 and its products.
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KONTIAINEN, S., SIMPSON, E., BOHRER, E. et al. T-cell lines producing antigen-specific suppressor factor. Nature 274, 477–480 (1978). https://doi.org/10.1038/274477a0
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DOI: https://doi.org/10.1038/274477a0
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