Anti-tumour activity of heat-shock protein 60-recognizing CD4+ T cells against syngeneic murine renal cell carcinoma

Masatoshi Eto, Mamoru Harada, Katsunori Tatsugami, Masahiko Harano, Hirofumi Koga, Goro Matsuzaki, Seiji Naito

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)


OBJECTIVES: To determine whether heat-shock protein (HSP) 60-recognizing CD4+ T cells show antitumour activity against renal carcinoma (RENCA) cells, as HSP is highly expressed by tumour cells and induced in cells by various stresses, including transformation. MATERIALS AND METHODS: RENCA, a renal cortical adenocarcinoma cell line of BALB/c origin, was used. Expression of major histocompatibility complex (MHC) class I, class II and HSP-60 on RENCA tumour cells was analysed by flow cytometry. BASL1.1, an autoreactive T-helper type 1 type CD4+ T cell clone established by us, and that recognises HSP-60, was also used for a tumour-neutralising assay. RESULTS: The RENCA cells were negative for MHC class II, but expressed intracellular HSP-60. In the tumour-neutralising assay, BASL1.1 cells significantly suppressed the in vivo growth of RENCA cells. Three of five mice rejected RENCA cells when co-inoculated with BASL1.1 cells. CONCLUSIONS: These results indicate that HSP-60-recognizing CD4+ T cells have the potential to eliminate renal cell carcinoma in vivo and that the eliciting of an anti-self T cell response at the tumour site can lead to regression of renal cancer.

Original languageEnglish
Pages (from-to)421-424
Number of pages4
JournalBJU international
Issue number3
Publication statusPublished - Feb 2005

All Science Journal Classification (ASJC) codes

  • Urology

Fingerprint Dive into the research topics of 'Anti-tumour activity of heat-shock protein 60-recognizing CD4<sup>+</sup> T cells against syngeneic murine renal cell carcinoma'. Together they form a unique fingerprint.

Cite this