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- W266670018 abstract "Major histocompatibility complex (MHC)-restricted cytolytic T lymphocytes (CTL) are generated in response to allogeneic tissues (normal and malignant), tumors (autologous and syngeneic), viruses, and certain bacteria and self-antigens. CTL can be derived directly from spleen or lymph nodes after immunization, but these cells often require a secondary in vitro stimulation (Cerottini and Brunner. 1974). Peritoneal exudate CTL (PEL), collected during or shortly after a primary intraperitoneal (i.p.) immunization of rats and mice with allogeneic or irradiated syngeneic tumors, usually yield a highly potent, specific population of CTL (Berke et al., 1972a, 1972b, 1972c; Fishelson and Berke, 1978; Schick and Berke, 1977; Berke and Schick, 1980). Generation of PEL can be augmented by, but does not require, a secondary stimulation in vivo or in vitro." @default.
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- W266670018 date "1993-01-01" @default.
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- W266670018 title "Immunobiology and Molecular Characteristics of Peritoneal Exudate Cytotoxic T Lymphocytes (PEL), Their In Vivo IL-2-Dependent Blasts and IL-2-Independent Cytolytic Hybridomas" @default.
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- W266670018 doi "https://doi.org/10.1007/978-1-4684-6814-4_10" @default.
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