Cellular immune reactivity in vitro and tumor rejection provided by tumor-associated antigens of friend-virus-induced leukemia

✍ Scribed by J. H. Dean; J. L. McCoy; L. W. Law; B. A. Maurer; E. Appella

• Publisher: John Wiley and Sons
• Year: 1975
• Tongue: French
• Weight: 830 KB
• Volume: 16
• Category: Article
• ISSN: 0020-7136
• DOI: 10.1002/ijc.2910160502

✦ Synopsis

Abstract

Cell‐mediated immunity (CMI) and tumor rejection were studied in the Friend virus leukemia system of C57BI/6 mice. Mice were immunized with Friend leukemia virus (FLV) or X‐irradiated FBL‐3 leukemic cells and studied temporally for the development of CMI reactivity by assays of ^51^Cr release lymphocyte cytotoxicity, lymphocyte transformation, migration inhibition, Winn tumor cell neutralization and transplantation rejection. High levels of specific lymphocyte cytotoxicity were observed by day 7 following FLV infection; this reactivity reached a peak between 17 and 21 days, and returned to background levels by day 36. Further, positive Winn assays were obtained with spleen cells from mice immunized with FLV at times when the mice resisted live FBL‐3 tumor challenge. Positive lymphocyte transformation was obtained with spleen cells from mice immunized with FLV or FBL‐3, but not with cells from normal mice or mice immune to a syngeneic methycholanthrene‐induced tumor, when cultured with papain‐soluble FBL‐3 or RBL‐5 tumor‐cell extracts or mitomycin‐C (MMC)‐treated FBL‐3 or RBL‐5 cells. Positive reactivity in the lymphocyte transformation assay occurred after reactivity had peaked in the lymphocyte cytotoxicity test. Similar positive macrophage migration inhibition patterns were also obtained with peritoneal exudate cells (PEC) from FLV‐immunized mice using papain‐solubilized tumor‐associated antigen (TAA) from FBL‐3 cells. These data suggest that sequential development and modulation of CMI reactivity occurs as observed in different assays following immunization in this system.