## Abstract A large dose of tumour cells (10^7^) from two different tumours produced a significant increase of Igโbearing spleen cells 6 h after intraperitoneal administration in syngeneic mice, like conventional antigens previously tested. Incubation of normal spleen cells in serum taken 6 h after
Surface membrane changes of T cells induced by syngeneic tumour cells. II. T-cell defects induced by small tumour cell inocula or tumour cell antigens
โ Scribed by D. A. Chow; Dr. F. Paraskevas; U. Dular
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- French
- Weight
- 851 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
Injection of a large number of tumour cells, like other strong immunogenic challenges, is followed within 6 h by the uptake of cytophilic Ig (probably complexes) by a subpopulation of T cells. This phenomenon, known as the โ6โhour Tโcell responseโ is abrogated when small tumour cell inocula (10^2^), or small amounts of a preparation from tumour cells, which contains tumour antigens, are injected prior to the immunogenic challenge Abrogation of the โ6โhour Tโcell responseโ resulted in a decrease in specific antiโtumour cell immunity as tested in vitro by measuring growth inhibition (cytostasis). It has also resulted in loss of the amplifying function on antibody formation against sheep erythrocytes, normally detected in a TโB cell coโoperative system when T cells are used 6 h after priming with sheep erythrocytes. It is postulated that this Tโcell defect may represent a mechanism by which tumour cells, in the early stages of their growth, interfere with inductive stages of the immune response for a sufficient period of time to allow the tumour to grow beyond immune control.
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