PMID- 8402448 OWN - NLM STAT- MEDLINE DCOM- 19931112 LR - 20190620 IS - 0008-543X (Print) IS - 0008-543X (Linking) VI - 72 IP - 8 DP - 1993 Oct 15 TI - Characterization of lung squamous cell carcinoma-derived T-cell suppressive factor. PG - 2347-57 AB - BACKGROUND: The immunosuppressive state of a tumor-bearing patient is possibly mediated by tumor-derived factor. In this study, the authors characterized lung squamous cell carcinoma-derived immunosuppressive factor (LSCF). METHODS: The immunosuppressive activity of QG56 (a lung squamous carcinoma cell line)-derived LSCF was evaluated by the effect of culture supernatant of QG56 on anti-CD3 monoclonal antibody-induced T-cell, response such as proliferation (3H-thymidine uptake), cytotoxicity (51Cr-releasing assay), and expression of cytokine mRNA (polymerase chain reaction). The LSCF was partially purified with an ion-exchange high-performance liquid chromatography (HPLC) and a gel-filtration HPLC. RESULTS: The LSCF inhibited proliferation, cytotoxicity, and expression of cytokine mRNA of T-cells in a dose-dependent manner. It has a molecular weight of approximately 22 kd, and was sensitive to proteinase K, heating at 60 degrees C, and resistant to treatment with trypsin and pH 3 and 9. These properties appear to be similar to those of transforming growth factor-beta (TGF-beta). However, the activity of the LSCF was not abrogated by anti-TGF-beta sera, and the LSCF did not suppress the proliferation of TGF-beta-sensitive mink lung cells (Mv1Lu). CONCLUSIONS: These data suggest that LSCF may be a novel tumor-derived immunosuppressive protein factor. FAU - Yoshino, I AU - Yoshino I AD - Department of Virology, Kyushu University, Fukuoka, Japan. FAU - Yano, T AU - Yano T FAU - Miyamoto, M AU - Miyamoto M FAU - Yamada, K AU - Yamada K FAU - Kajii, Y AU - Kajii Y FAU - Onodera, K AU - Onodera K FAU - Ishida, T AU - Ishida T FAU - Sugimachi, K AU - Sugimachi K FAU - Kimura, G AU - Kimura G FAU - Nomoto, K AU - Nomoto K LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Cancer JT - Cancer JID - 0374236 RN - 0 (CD3 Complex) RN - 0 (Cytokines) RN - 0 (DNA Primers) RN - 0 (Interleukin-2) RN - 0 (RNA, Messenger) RN - 0 (Receptors, Interleukin-2) RN - 0 (Suppressor Factors, Immunologic) RN - 0 (Transforming Growth Factor beta) SB - IM MH - Base Sequence MH - CD3 Complex/immunology MH - Carcinoma, Squamous Cell/*immunology/metabolism MH - Cytokines/genetics MH - Cytotoxicity, Immunologic MH - DNA Primers MH - Humans MH - Interleukin-2/metabolism MH - Lung Neoplasms/*immunology/metabolism MH - Lymphocyte Activation MH - Molecular Sequence Data MH - Molecular Weight MH - RNA, Messenger/metabolism MH - Receptors, Interleukin-2/metabolism MH - Suppressor Factors, Immunologic/metabolism/*physiology MH - T-Lymphocytes/*immunology/metabolism MH - Transforming Growth Factor beta/physiology MH - Tumor Cells, Cultured EDAT- 1993/10/15 00:00 MHDA- 1993/10/15 00:01 CRDT- 1993/10/15 00:00 PHST- 1993/10/15 00:00 [pubmed] PHST- 1993/10/15 00:01 [medline] PHST- 1993/10/15 00:00 [entrez] AID - 10.1002/1097-0142(19931015)72:8<2347::aid-cncr2820720810>3.0.co;2-i [doi] PST - ppublish SO - Cancer. 1993 Oct 15;72(8):2347-57. doi: 10.1002/1097-0142(19931015)72:8<2347::aid-cncr2820720810>3.0.co;2-i.