Protective effects of interferon-γ on squamous-cell carcinoma of head and neck targets in antibody-dependent cellular cytotoxicity mediated by human natural killer cells

Myung Whun Sung, Jonas T. Johnson, Guus Van Dongen, Theresa L. Whiteside

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

An in vitro model of antibody-dependent cellular cytotoxicity (ADCC) was established, using squamous-cell carcinoma of the head and neck (SCCHN) targets, human/mouse chimeric monoclonal antibodies (cMAbs) SF-25 and 323/A3 and human peripheral blood mononuclear cells (PBMC). We previously showed that natural killer (NK) cells are the main effector population mediating ADCC in the presence of the cMAbs. ADCC was significantly inhibited by the overnight pretreatment of SCCHN targets with exogenous interferon-γ (IFN-γ). This inhibition was dose-dependent, reproducible and consistently observed with various SCCHN cell lines. SCCHN cells pre-treated with IFN-γ had a significantly higher expression of intercellular adhesion molecule-1 (ICAM-1) and major histocompatibility complex (MHC) class 1 antigens compared with untreated target cells. No differences in expression of the SCCHN-associated antigens on these targets or in the formation of NK-SCCHN conjugates were found, using flow cytometry. IFN-γ-pre-treated SCCHN cells were less effective in competing with untreated targets in cold target inhibition assays and in inducing cytokine production from NK cells in co-incubation experiments. Protective effects of IFN-γ on target cell sensitivity to lysis were blocked by pre-treatment of target cells with actinomycin-D or cycloheximide. The susceptibility of the target cells was restored by removal of MHC class I antigens from their surface by acid stripping before ADCC. Our results suggest that the decreased ADCC seen with SCCHN targets pre-treated with IFN-γ is related to post-binding events, possibly altered signaling from targets to effector cells, and requires protein synthesis in the target cells.

Original languageEnglish
Pages (from-to)393-399
Number of pages7
JournalInternational Journal of Cancer
Volume66
Issue number3
DOIs
Publication statusPublished - 3 May 1996

Cite this

@article{1bf976c0bd624e0aa0b23dcce1cebb7a,
title = "Protective effects of interferon-γ on squamous-cell carcinoma of head and neck targets in antibody-dependent cellular cytotoxicity mediated by human natural killer cells",
abstract = "An in vitro model of antibody-dependent cellular cytotoxicity (ADCC) was established, using squamous-cell carcinoma of the head and neck (SCCHN) targets, human/mouse chimeric monoclonal antibodies (cMAbs) SF-25 and 323/A3 and human peripheral blood mononuclear cells (PBMC). We previously showed that natural killer (NK) cells are the main effector population mediating ADCC in the presence of the cMAbs. ADCC was significantly inhibited by the overnight pretreatment of SCCHN targets with exogenous interferon-γ (IFN-γ). This inhibition was dose-dependent, reproducible and consistently observed with various SCCHN cell lines. SCCHN cells pre-treated with IFN-γ had a significantly higher expression of intercellular adhesion molecule-1 (ICAM-1) and major histocompatibility complex (MHC) class 1 antigens compared with untreated target cells. No differences in expression of the SCCHN-associated antigens on these targets or in the formation of NK-SCCHN conjugates were found, using flow cytometry. IFN-γ-pre-treated SCCHN cells were less effective in competing with untreated targets in cold target inhibition assays and in inducing cytokine production from NK cells in co-incubation experiments. Protective effects of IFN-γ on target cell sensitivity to lysis were blocked by pre-treatment of target cells with actinomycin-D or cycloheximide. The susceptibility of the target cells was restored by removal of MHC class I antigens from their surface by acid stripping before ADCC. Our results suggest that the decreased ADCC seen with SCCHN targets pre-treated with IFN-γ is related to post-binding events, possibly altered signaling from targets to effector cells, and requires protein synthesis in the target cells.",
author = "Sung, {Myung Whun} and Johnson, {Jonas T.} and {Van Dongen}, Guus and Whiteside, {Theresa L.}",
year = "1996",
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language = "English",
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journal = "International Journal of Cancer",
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Protective effects of interferon-γ on squamous-cell carcinoma of head and neck targets in antibody-dependent cellular cytotoxicity mediated by human natural killer cells. / Sung, Myung Whun; Johnson, Jonas T.; Van Dongen, Guus; Whiteside, Theresa L.

In: International Journal of Cancer, Vol. 66, No. 3, 03.05.1996, p. 393-399.

Research output: Contribution to journalArticleAcademicpeer-review

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T1 - Protective effects of interferon-γ on squamous-cell carcinoma of head and neck targets in antibody-dependent cellular cytotoxicity mediated by human natural killer cells

AU - Sung, Myung Whun

AU - Johnson, Jonas T.

AU - Van Dongen, Guus

AU - Whiteside, Theresa L.

PY - 1996/5/3

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N2 - An in vitro model of antibody-dependent cellular cytotoxicity (ADCC) was established, using squamous-cell carcinoma of the head and neck (SCCHN) targets, human/mouse chimeric monoclonal antibodies (cMAbs) SF-25 and 323/A3 and human peripheral blood mononuclear cells (PBMC). We previously showed that natural killer (NK) cells are the main effector population mediating ADCC in the presence of the cMAbs. ADCC was significantly inhibited by the overnight pretreatment of SCCHN targets with exogenous interferon-γ (IFN-γ). This inhibition was dose-dependent, reproducible and consistently observed with various SCCHN cell lines. SCCHN cells pre-treated with IFN-γ had a significantly higher expression of intercellular adhesion molecule-1 (ICAM-1) and major histocompatibility complex (MHC) class 1 antigens compared with untreated target cells. No differences in expression of the SCCHN-associated antigens on these targets or in the formation of NK-SCCHN conjugates were found, using flow cytometry. IFN-γ-pre-treated SCCHN cells were less effective in competing with untreated targets in cold target inhibition assays and in inducing cytokine production from NK cells in co-incubation experiments. Protective effects of IFN-γ on target cell sensitivity to lysis were blocked by pre-treatment of target cells with actinomycin-D or cycloheximide. The susceptibility of the target cells was restored by removal of MHC class I antigens from their surface by acid stripping before ADCC. Our results suggest that the decreased ADCC seen with SCCHN targets pre-treated with IFN-γ is related to post-binding events, possibly altered signaling from targets to effector cells, and requires protein synthesis in the target cells.

AB - An in vitro model of antibody-dependent cellular cytotoxicity (ADCC) was established, using squamous-cell carcinoma of the head and neck (SCCHN) targets, human/mouse chimeric monoclonal antibodies (cMAbs) SF-25 and 323/A3 and human peripheral blood mononuclear cells (PBMC). We previously showed that natural killer (NK) cells are the main effector population mediating ADCC in the presence of the cMAbs. ADCC was significantly inhibited by the overnight pretreatment of SCCHN targets with exogenous interferon-γ (IFN-γ). This inhibition was dose-dependent, reproducible and consistently observed with various SCCHN cell lines. SCCHN cells pre-treated with IFN-γ had a significantly higher expression of intercellular adhesion molecule-1 (ICAM-1) and major histocompatibility complex (MHC) class 1 antigens compared with untreated target cells. No differences in expression of the SCCHN-associated antigens on these targets or in the formation of NK-SCCHN conjugates were found, using flow cytometry. IFN-γ-pre-treated SCCHN cells were less effective in competing with untreated targets in cold target inhibition assays and in inducing cytokine production from NK cells in co-incubation experiments. Protective effects of IFN-γ on target cell sensitivity to lysis were blocked by pre-treatment of target cells with actinomycin-D or cycloheximide. The susceptibility of the target cells was restored by removal of MHC class I antigens from their surface by acid stripping before ADCC. Our results suggest that the decreased ADCC seen with SCCHN targets pre-treated with IFN-γ is related to post-binding events, possibly altered signaling from targets to effector cells, and requires protein synthesis in the target cells.

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JF - International Journal of Cancer

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