Literature DB >> 1828007

Modulation of the immune response to tumors by a novel synthetic compound, (4R)-3-benzoyl-N-[(1R)-1-phenylethyl]-4-thiazolidinecarboxamide (RS-0481).

S Kurakata1, M Tomatsu, M Arai, H Arai, A Hishinuma, H Kohno, K Kitamura, T Kobayashi, K Nomoto.   

Abstract

RS-0481, (4R)-3-benzoyl-N-[(1R)-phenylethyl]-4-thiazolidinecarboxamide, is a compound that can re-establish the function of certain lymphoid cell populations impaired by the presence of a growing tumor in an animal. The compound markedly augmented the tumor-specific cytotoxic T lymphocytes, TDTH (delayed-type hypersensitivity T cells), and the nonspecific lymphokine-activated-killer-cell-like cell responses. It also enhanced the tumor-inhibitory effect of macrophages in tumor-bearing mice, but not in normal mice, indicating that it enhances the antitumor immune responses. Lymphocytes from RS-0481-treated tumor-bearing mice released significantly higher amounts of macrophage-activating factor(s) (MAF) and interleukin-2(IL-2)-like factors in culture compared with lymphocytes from untreated animals. Also, sera from treated tumor bearers showed elevated colony-stimulating factor (CSF) activity. Although the compound did not influence the factor-producing activity in mice without tumor, it enhanced the responsiveness of their bone marrow cells, T cells, and macrophages to CSF, IL-2, and MAF. It seems therefore possible that the compound enhances the responsiveness of immunocompetent cells to cytokines, resulting in a marked augmentation of antitumor T cell responses in tumor-bearing mice. Consistently it inhibited the development of lymph node metastasis of transplanted X5563 plasmacytoma, and we showed that T cells play a decisive role in this inhibition. The compound also counteracted the development of suppressor T cell activity in the spleen of tumor-bearing mice.

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Year:  1991        PMID: 1828007     DOI: 10.1007/bf01742532

Source DB:  PubMed          Journal:  Cancer Immunol Immunother        ISSN: 0340-7004            Impact factor:   6.968


  24 in total

1.  Immunological surveillance in neoplasia.

Authors:  F M Burnet
Journal:  Transplant Rev       Date:  1971

2.  Impaired immunologic reactivity and recurrence following cancer surgery.

Authors:  F R Eilber; D L Morton
Journal:  Cancer       Date:  1970-02       Impact factor: 6.860

3.  Natural cytotoxicity in man: activity of lymph node and tumor-infiltrating lymphocytes.

Authors:  B M Vose; F Vánky; S Argov; E Klein
Journal:  Eur J Immunol       Date:  1977-11       Impact factor: 5.532

4.  The augmentation of in vitro and in vivo tumor-specific T cell-mediated immunity by amplifier T lymphocytes.

Authors:  H Fujiwara; T Hamaoka; G M Shearer; H Yamamoto; W D Terry
Journal:  J Immunol       Date:  1980-02       Impact factor: 5.422

5.  Origin and function of suppressor macrophages in myeloma.

Authors:  J Kennard; S Zolla-Pazner
Journal:  J Immunol       Date:  1980-01       Impact factor: 5.422

6.  Macrophage-dependent, NK-cell-independent "natural" surveillance of tumors in syngeneic mice.

Authors:  D A Chow; M I Greene; A H Greenberg
Journal:  Int J Cancer       Date:  1979-06-15       Impact factor: 7.396

7.  Studies on macrophage-activating factor (MAF) in antitumor immune responses. I. Tumor-specific Lyt-1+2- T cells are required for producing MAF able to generate cytolytic as well as cytostatic macrophages.

Authors:  H Nakajima; H Fujiwara; Y Takai; Y Izumi; S Sano; T Tsuchida; T Hamaoka
Journal:  J Immunol       Date:  1985-09       Impact factor: 5.422

8.  Partial purification and chemical characterization of macrophage cytotoxicity factor (MCF, MAF) and its separation from migration inhibitory factor (MIF).

Authors:  E M Kniep; W Domzig; M L Lohmann-Matthes; B Kickhöfen
Journal:  J Immunol       Date:  1981-08       Impact factor: 5.422

Review 9.  Immune surveillance and natural resistance: an evaluation.

Authors:  W Den Otter
Journal:  Cancer Immunol Immunother       Date:  1986       Impact factor: 6.968

10.  Systemic administration of interleukin-2 in humans.

Authors:  M T Lotze; R J Robb; S O Sharrow; L W Frana; S A Rosenberg
Journal:  J Biol Response Mod       Date:  1984-10
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