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An anti-MUC1-antibody-interleukin-2 fusion protein that activates resting NK cells to lysis of MUC1-positive tumour cells.

Heuser C, Ganser M, Hombach A, Brand H, Denton G, Hanisch FG, Abken H - Br. J. Cancer (2003)

Bottom Line: MUC1 mucin is aberrantly glycosylated and overexpressed in a number of epithelial malignancies and is therefore a promising tumour-associated antigen for target-directed immunotherapy of a panel of malignant diseases.To activate lymphocytes and natural killer (NK) cells, we here generated an anti-MUC1-scFv-IL2 fusion protein (C595scFv-Fc-IL2) that contains the C595 single-chain antibody for MUC1 binding, the human IgG1 CH2CH3 domain for protein dimerisation, and interleukin-2 (IL2) for activation of immunological effector cells.Bound to MUC1, the C595scFv-Fc-IL2 fusion protein stimulates proliferation of human activated lymphocytes in vitro.

View Article: PubMed Central - PubMed

Affiliation: Lab. Tumorgenetik, Klinik I für Innere Medizin, Klinikum der Universität zu Köln, Joseph-Stelzmann-Str. 9, D-50931 Köln, Germany.

ABSTRACT
MUC1 mucin is aberrantly glycosylated and overexpressed in a number of epithelial malignancies and is therefore a promising tumour-associated antigen for target-directed immunotherapy of a panel of malignant diseases. In MUC1-positive tumours, MHC class I expression is frequently downregulated and MUC1-specific cytotoxic T cells (CTLs) are either not available or in a state of anergy allowing tumour growth without limitation by CTL control. To activate lymphocytes and natural killer (NK) cells, we here generated an anti-MUC1-scFv-IL2 fusion protein (C595scFv-Fc-IL2) that contains the C595 single-chain antibody for MUC1 binding, the human IgG1 CH2CH3 domain for protein dimerisation, and interleukin-2 (IL2) for activation of immunological effector cells. The fusion protein binds to MUC1-derived peptides and to MUC1-positive tumour cells with the same specificity as does the C595 monoclonal antibody. Bound to MUC1, the C595scFv-Fc-IL2 fusion protein stimulates proliferation of human activated lymphocytes in vitro. Upon binding to MUC1-positive MCF7 breast carcinoma cells, moreover, the fusion protein activates resting NK cells to tumour cell lysis. These properties make the C595scFv-Fc-IL2 fusion protein a suitable candidate for the immunotherapy of MUC1-positive tumours.

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Related in: MedlinePlus

Activated lymphocytes proliferate in the presence of soluble C595scFv-Fc-IL2 fusion protein. Lymphocytes from the peripheral blood (2.5 × 105 cells per well) were activated by incubation with the anti-CD3 mAb OKT3 plus IL2 and cultured in the presence of cell culture supernatants containing the fusion proteins C595scFv-Fc-IL2 (•), C595scFv-Fc (▪), and as control IL2 (▴) (2 000 U ml−1), respectively. After 72 h, lymphocyte proliferation was quantified by means of the ‘XTT cell proliferation kit’ (Roche Diagnostics). The assays were performed in triplicate; data are presented as mean±s.e.m.
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fig7: Activated lymphocytes proliferate in the presence of soluble C595scFv-Fc-IL2 fusion protein. Lymphocytes from the peripheral blood (2.5 × 105 cells per well) were activated by incubation with the anti-CD3 mAb OKT3 plus IL2 and cultured in the presence of cell culture supernatants containing the fusion proteins C595scFv-Fc-IL2 (•), C595scFv-Fc (▪), and as control IL2 (▴) (2 000 U ml−1), respectively. After 72 h, lymphocyte proliferation was quantified by means of the ‘XTT cell proliferation kit’ (Roche Diagnostics). The assays were performed in triplicate; data are presented as mean±s.e.m.

Mentions: We assessed the IL2 bioactivity of the C595scFv-Fc-IL2 fusion protein by monitoring the induction of proliferation of activated lymphocytes. As shown in Figure 7Figure 7


An anti-MUC1-antibody-interleukin-2 fusion protein that activates resting NK cells to lysis of MUC1-positive tumour cells.

Heuser C, Ganser M, Hombach A, Brand H, Denton G, Hanisch FG, Abken H - Br. J. Cancer (2003)

Activated lymphocytes proliferate in the presence of soluble C595scFv-Fc-IL2 fusion protein. Lymphocytes from the peripheral blood (2.5 × 105 cells per well) were activated by incubation with the anti-CD3 mAb OKT3 plus IL2 and cultured in the presence of cell culture supernatants containing the fusion proteins C595scFv-Fc-IL2 (•), C595scFv-Fc (▪), and as control IL2 (▴) (2 000 U ml−1), respectively. After 72 h, lymphocyte proliferation was quantified by means of the ‘XTT cell proliferation kit’ (Roche Diagnostics). The assays were performed in triplicate; data are presented as mean±s.e.m.
© Copyright Policy
Related In: Results  -  Collection

Show All Figures
getmorefigures.php?uid=PMC2376954&req=5

fig7: Activated lymphocytes proliferate in the presence of soluble C595scFv-Fc-IL2 fusion protein. Lymphocytes from the peripheral blood (2.5 × 105 cells per well) were activated by incubation with the anti-CD3 mAb OKT3 plus IL2 and cultured in the presence of cell culture supernatants containing the fusion proteins C595scFv-Fc-IL2 (•), C595scFv-Fc (▪), and as control IL2 (▴) (2 000 U ml−1), respectively. After 72 h, lymphocyte proliferation was quantified by means of the ‘XTT cell proliferation kit’ (Roche Diagnostics). The assays were performed in triplicate; data are presented as mean±s.e.m.
Mentions: We assessed the IL2 bioactivity of the C595scFv-Fc-IL2 fusion protein by monitoring the induction of proliferation of activated lymphocytes. As shown in Figure 7Figure 7

Bottom Line: MUC1 mucin is aberrantly glycosylated and overexpressed in a number of epithelial malignancies and is therefore a promising tumour-associated antigen for target-directed immunotherapy of a panel of malignant diseases.To activate lymphocytes and natural killer (NK) cells, we here generated an anti-MUC1-scFv-IL2 fusion protein (C595scFv-Fc-IL2) that contains the C595 single-chain antibody for MUC1 binding, the human IgG1 CH2CH3 domain for protein dimerisation, and interleukin-2 (IL2) for activation of immunological effector cells.Bound to MUC1, the C595scFv-Fc-IL2 fusion protein stimulates proliferation of human activated lymphocytes in vitro.

View Article: PubMed Central - PubMed

Affiliation: Lab. Tumorgenetik, Klinik I für Innere Medizin, Klinikum der Universität zu Köln, Joseph-Stelzmann-Str. 9, D-50931 Köln, Germany.

ABSTRACT
MUC1 mucin is aberrantly glycosylated and overexpressed in a number of epithelial malignancies and is therefore a promising tumour-associated antigen for target-directed immunotherapy of a panel of malignant diseases. In MUC1-positive tumours, MHC class I expression is frequently downregulated and MUC1-specific cytotoxic T cells (CTLs) are either not available or in a state of anergy allowing tumour growth without limitation by CTL control. To activate lymphocytes and natural killer (NK) cells, we here generated an anti-MUC1-scFv-IL2 fusion protein (C595scFv-Fc-IL2) that contains the C595 single-chain antibody for MUC1 binding, the human IgG1 CH2CH3 domain for protein dimerisation, and interleukin-2 (IL2) for activation of immunological effector cells. The fusion protein binds to MUC1-derived peptides and to MUC1-positive tumour cells with the same specificity as does the C595 monoclonal antibody. Bound to MUC1, the C595scFv-Fc-IL2 fusion protein stimulates proliferation of human activated lymphocytes in vitro. Upon binding to MUC1-positive MCF7 breast carcinoma cells, moreover, the fusion protein activates resting NK cells to tumour cell lysis. These properties make the C595scFv-Fc-IL2 fusion protein a suitable candidate for the immunotherapy of MUC1-positive tumours.

Show MeSH
Related in: MedlinePlus