Abstract
Peritoneal exudate cells (PEC), obtained after the rejection of EL4 leukemia by BALB/c mice, are much more effective in the specific in vitro destruction of (51)Cr-labeled EL4 cells than are spleen, thymus, lymph node, or peripheral blood lymphocytes. The presence of a large number of effector cells at the site of graft rejection is reflected in the potent cytolytic activity seen in vitro. Effector cells temporarily lose cytolytic reactivity when treated with trypsin but regain reactivity with time. This recovery occurs in normal as well as in immune serum. The destructive reactivity of PEC is increased when macrophages are removed. The remaining population of nonadherent PEC is composed primarily of small- to medium-sized lymphocytes. Complex tissue culture media are not needed, but there is a definite requirement for serum. The required serum component is heat stable, nondialyzable, and is not consumed during the reaction. The use of an ascites allograft system made these observations possible and permitted the isolation of those host cells intimately associated with rejection.
MeSH Terms
Animals
Chromium/metabolism
Chromium Isotopes
Cytotoxicity Tests, Immunologic
Exudates and Transudates/immunology
Female
Freezing
Graft Rejection
In Vitro Techniques
Leukemia, Experimental/immunology
Lymph Nodes/cytology,immunology
Lymphoid Tissue/immunology
Male
Mice
Mice, Inbred Strains
Neoplasm Transplantation
Peritoneal Cavity/cytology
Peyer's Patches/cytology,immunology
Spleen/cytology,immunology
Thymus Gland/cytology,immunology
Transplantation Immunology
Trypsin
Chemicals
Chromium Isotopes
Chromium
Trypsin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Berke G
Sullivan K A
Amos B
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