The effects of a new metalloproteinase inhibitor, BE 16627B [L-N-(N-hydroxy-2-isobutylsuccinynamoyl)-se~l-L-valine, M W 375.21 isolated from microbial cultures, on human tumor cell growth in nude mice were investigated. BEl6627B inhibited metalloproteinases in enzyme assays, as well as gelatinolysis
Inhibition of the growth of human melanoma xenografts in nude mice by human tumor-specific cytotoxic T-cells
โ Scribed by Nancy J. Crowley; Craig L. Slingluff Jr.; Carol E. Vervaert; Timothy L. Darrow; Hilliard F. Seigler
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 538 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0022-4790
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โฆ Synopsis
Melanoma-specific T-cells (CTLs) are specifically cytotoxic for autologous tumor, when assayed in vitro. To examine their effectiveness in vivo, we tested the ability of these human T-cells to inhibit growth of human melanoma xenografts by using a Winn assay. Nude mice receiving specific CTLs (n = 10) demonstrated a dramatic inhibition of tumor growth. All treated mice were tumor-free at day SO and nine remained tumor-free at day 6.5, vs. control mice (n= 10) with average tumor volumes of 321 mm3 and 808 mm3, respectively. To control for the possibility that a non-specific response to the human T-cells could inhibit tumor growth, an additional group received allospecific CTLs. There was no inhibition of tumor growth in this group (n = 8), with the average tumor volume of 2,768 mm' at day 40 vs. 1,882 mm3 in the control group (n= 10). We conclude that these tumor-specific CTLs can inhibit tumor growth in vivo and may prove useful in the adoptive immunotherapy of melanoma.
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The study of specific immunity in human cancers has been hampered by the elusive distribution and heterogeneity of effector cells. In this study, we have investigated the distribution of autologous melanoma-specific cytotoxic T lymphocytes (CTLs) in 18 different distant metastases from melanomas (9