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Adoptive transfer of cell-mediated immunity to specific antigens in humans was first demonstrated by Lawrence (1) in 1949, thus opening a new avenue of research that has led both to increased understanding of basic immune mechanisms and to the development of immunomodulation therapy. Law rence originally showed that transfer of whole viable lymphocytes from a normal tuberculin skin test-positive donor to a normal skin test-negative recipient resulted in a conversion of the recipient to skin-test positivity, but this observation created little interest in the immunologic community for several reasons. In 1955, the lymphocyte was mentioned for the first time as a possible immunologic organ. Traditionally, the lymphocyte had been studied in hematologic rather than in immunologic terms . In the third edition of his classic textbook on the anatomy of the lymphoid system, Professor A. Joffy of the University of Bristol proposed three questions to lymphocytes: Where do you come from, where do you go and what do you do, if anything? In 1962(2) , 1. Miller showed that the immune system in chickens could be divided into two components , namely the B lymphocyte derived from the bursal system (B cell) producing antibodies that protect against infection from microorganisms (pneumococcus , meningococcus, streptococcus, gonococ cus, etc) and thymic-dependent (T cell) systems that protect against fungi, parasites , viruses, mycobacteria, and cancer metastases . Previously, Law rence (3) demonstrated that delayed cutaneous hypersensitivity (DH) respon siveness could also be transferred by soluble extracts of leukocytes
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Fudenberg et al. (1989) studied this question.
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