## Abstract It has been shown that tumour‐specific antigen from a chemically‐induced rat hepatoma is capable of binding to immunoadsorbent columns made from the Ig fractions of antisera raised in allogeneic animals against a variety of normal tissues. This reactivity is observed with antisera direc
Tumour antigens and alloantigens. II. Lack of association of rat hepatoma-D23-specific antigen with β2 microglobulin
✍ Scribed by J. Gareth Bowen; R. W. Baldwin
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- French
- Weight
- 672 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0020-7136
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✦ Synopsis
Abstract
It has previously been shown that the tumourspecific antigen of the chemically‐induced rat hepatoma D23 has determinants recognised by alloantisera raised against normal syngeneic liver and spleen. However, no reactions were observed with alloantisera raised against syngeneic erythrocytes suggesting that the alloantigenic determinant responsible for this cross‐reactivity is not a major serologically‐defined histocompatibility antigen. This concept has been further examined using a defined turkey anti‐rat β~2~ microglobulin antiserum. This antiserum failed to block the binding of syngeneic antihepatoma D23 sera to hepatoma D23 target cells as assessed using membrane immunofluorescence and complement‐dependant ^51^Cr release tests. Furthermore, immune precipitates formed from soluble tumour extracts containing hepatoma D23 specific antigen with turkey anti‐rat β~2~ microglobulin failed to generate a tumour‐specific antibody response in syngeneic rats although a cross‐reactive antiserum was produced following immunization of allogeneic rats with the immune precipitate.
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## Abstract Cellular and humoral immune reactions against tumour‐specific antigens on aminoazo‐dye‐induced rat hepatomas were demonstrated __in vitro__ by the colony inhibition technique. Lymph‐node cells from syngeneic rats immunized against individual hepatomas inhibited colony formation by cells