## Abstract A solubilization technique employing 0.5% Triton X‐100 was developed to obtain both SV40 virus (SV40)‐induced tumor‐specific surface antigen(s) (TSSA) from SV40‐transformed mouse cells, as determined by a serum‐mediated microcytolytic assay, and tumor‐specific transplantation antigen(s)
Distinction between tumor-specific transplantation antigen and virion antigens in solubilized products from membranes of virus-induced leukemic cells
✍ Scribed by Kenneth S. S. Chang; Lloyd W. Law; Ettore Appella
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- French
- Weight
- 726 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0020-7136
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✦ Synopsis
Abstract
A membrane antigen from RBL‐5 leukemic cells that was solubilized and partially purified is further characterized in this study. This soluble antigen is capable of immunizing syngeneic hosts to reject neoplastic cells and thus resembles TSTA. It also induces cytotoxic antibody in syngeneic hosts capable of specifically lysing RBL‐5 cells in vitro. RBL‐5, however, releases infectious virus (RLV); it was necessary therefore to rule out virus or structural virion antigens as the effective immunogen. Infectious virus was not detectable in our initial crude membrane (CM) material, nor in the papain‐solubilized CS or the G‐150 Sephadex‐chromatographed fraction. Virus‐neutralizing antibody was not detected, under stringent assay conditions, in the syngeneic anti‐CM sera. Antigen preparations CM, CS and the chromatographed fractions F1, F2 and F3 were assayed in a complement‐fixation test against broad‐reacting antisera capable of detecting virus envelope antigen and gs antigen and against syngeneic antisera. Although our antigen preparations were positive for virion antigens. CS and F2 contained an antigen that reacted only with syngeneic antiserum. These same fractions were those reactive as immunogens. On the basis of these data, it is postulated that a cellular membrane component, other than viral, functions as TSTA.
📜 SIMILAR VOLUMES
## Abstract The immunogenicity of the SV40 tumor‐specific transplantation antigen (TSTA) on cells, cell particulates and solubilized membranes was studied in mice and in Syrian hamsters. Immunizations were done with various concentrations of tissue‐culture‐passaged, non‐virus‐releasing transformed