## Abstract Valproic acid (VA) is a well‐tolerated drug used to treat seizure disorders and has recently been shown to inhibit histone deacetylase (HDAC). Because HDAC modulates chromatin structure and gene expression, parameters considered to influence radioresponse, we investigated the effects of
In vitro cytotoxicity and in vivo tumor enhancement induced by mouse spleen cells autosensitized in vitro
✍ Scribed by David Ilfeld; Claude Carnaud; Irun R. Cohen; Nathan Trainin
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- French
- Weight
- 748 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The immuno‐reactivity of C57BL mouse spleen cells previously sensitized in vitro against syngeneic fibroblasts or syngeneic 3LL Lewis tumor cells was investigated. The sensitized spleen cells were assayed in vitro to test their cytotoxicity against the 3LL tumor cells. In addition, spleen cells autosensitized against syngeneic fibroblasts were mixed with 3LL tumor cells and injected into syngeneic recipient mice in order to ascertain their influence on tumor growth. The in vitro assay indicated that lymphoid cells specifically sensitized against either fibroblasts or tumor cells were equally cytotoxic against the 3LL target cells. On the other hand, in the in vivo experiments lymphoid cells sensitized against syngeneic fibroblasts promoted the growth of the 3LL tumor. An attempt to explain the underlying mechanisms involved in the paradoxical behavior of autosensitized lymphocytes is reported herein.
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