The immune privilege of the eye: human retinal pigment epithelial cells selectively modulate T-cell activation in vitro.

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

The immune privilege of the eye: human retinal pigment epithelial cells selectively modulate T-cell activation in vitro. / Kaestel, Charlotte G; Lovato, Paola; Ødum, Niels; Nissen, Mogens H; Röpke, Carsten.

In: Current Eye Research, Vol. 30, No. 5, 2005, p. 375-83.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Kaestel, CG, Lovato, P, Ødum, N, Nissen, MH & Röpke, C 2005, 'The immune privilege of the eye: human retinal pigment epithelial cells selectively modulate T-cell activation in vitro.', Current Eye Research, vol. 30, no. 5, pp. 375-83. https://doi.org/10.1080/02713680590934120

APA

Kaestel, C. G., Lovato, P., Ødum, N., Nissen, M. H., & Röpke, C. (2005). The immune privilege of the eye: human retinal pigment epithelial cells selectively modulate T-cell activation in vitro. Current Eye Research, 30(5), 375-83. https://doi.org/10.1080/02713680590934120

Vancouver

Kaestel CG, Lovato P, Ødum N, Nissen MH, Röpke C. The immune privilege of the eye: human retinal pigment epithelial cells selectively modulate T-cell activation in vitro. Current Eye Research. 2005;30(5):375-83. https://doi.org/10.1080/02713680590934120

Author

Kaestel, Charlotte G ; Lovato, Paola ; Ødum, Niels ; Nissen, Mogens H ; Röpke, Carsten. / The immune privilege of the eye: human retinal pigment epithelial cells selectively modulate T-cell activation in vitro. In: Current Eye Research. 2005 ; Vol. 30, No. 5. pp. 375-83.

Bibtex

@article{d3c7b290b93811ddae57000ea68e967b,
title = "The immune privilege of the eye: human retinal pigment epithelial cells selectively modulate T-cell activation in vitro.",
abstract = "PURPOSE: To examine the effect of human retinal pigment epithelial (RPE) cells on phytohemagglutinin (PHA) activation of T cells. METHODS: Resting peripheral blood lymphocytes (PBLs) were stimulated with PHA with or without the presence of gamma-irradiated RPE cells. Proliferation and the cell cycle profile were thereafter investigated by 3H-thymidine incorporation and flow cytometric analysis. In addition, the PBLs expression of CD69, major histocompatibility complex (MHC) class I and II, CD3, as well as the IL-2 receptor chains were evaluated by flow cytometry, and the content of IL-2 in cell culture supernatant was measured by ELISA. RESULTS: Human RPE cells were found to suppress PHA-induced proliferation, cyclin A, IL-2R-alpha and -gamma, and CD71 expression and decrease the production of IL-2; but RPE cells do not inhibit the PHA-induced expression of early activation markers CD69, MHC class I and II, and of cyclin D of the PBLs. CONCLUSIONS: These results are the first to indicate that RPE cells impede generation of activated T cells by interfering with the induction of high-affinity IL-2R-alphabetagamma, IL-2 production, and the expression of CD71 and cyclin A.",
author = "Kaestel, {Charlotte G} and Paola Lovato and Niels {\O}dum and Nissen, {Mogens H} and Carsten R{\"o}pke",
note = "Keywords: Antigens, CD; Antigens, CD3; Antigens, Differentiation, T-Lymphocyte; Cell Cycle; Cell Line; Cell Proliferation; Coculture Techniques; DNA Replication; Enzyme-Linked Immunosorbent Assay; Eye; Flow Cytometry; Histocompatibility Antigens Class I; Histocompatibility Antigens Class II; Humans; Immune System; Interleukin-2 Receptor alpha Subunit; Lymphocyte Activation; Pigment Epithelium of Eye; Receptors, Interleukin; T-Lymphocytes",
year = "2005",
doi = "10.1080/02713680590934120",
language = "English",
volume = "30",
pages = "375--83",
journal = "Current Eye Research",
issn = "0271-3683",
publisher = "Taylor & Francis",
number = "5",

}

RIS

TY - JOUR

T1 - The immune privilege of the eye: human retinal pigment epithelial cells selectively modulate T-cell activation in vitro.

AU - Kaestel, Charlotte G

AU - Lovato, Paola

AU - Ødum, Niels

AU - Nissen, Mogens H

AU - Röpke, Carsten

N1 - Keywords: Antigens, CD; Antigens, CD3; Antigens, Differentiation, T-Lymphocyte; Cell Cycle; Cell Line; Cell Proliferation; Coculture Techniques; DNA Replication; Enzyme-Linked Immunosorbent Assay; Eye; Flow Cytometry; Histocompatibility Antigens Class I; Histocompatibility Antigens Class II; Humans; Immune System; Interleukin-2 Receptor alpha Subunit; Lymphocyte Activation; Pigment Epithelium of Eye; Receptors, Interleukin; T-Lymphocytes

PY - 2005

Y1 - 2005

N2 - PURPOSE: To examine the effect of human retinal pigment epithelial (RPE) cells on phytohemagglutinin (PHA) activation of T cells. METHODS: Resting peripheral blood lymphocytes (PBLs) were stimulated with PHA with or without the presence of gamma-irradiated RPE cells. Proliferation and the cell cycle profile were thereafter investigated by 3H-thymidine incorporation and flow cytometric analysis. In addition, the PBLs expression of CD69, major histocompatibility complex (MHC) class I and II, CD3, as well as the IL-2 receptor chains were evaluated by flow cytometry, and the content of IL-2 in cell culture supernatant was measured by ELISA. RESULTS: Human RPE cells were found to suppress PHA-induced proliferation, cyclin A, IL-2R-alpha and -gamma, and CD71 expression and decrease the production of IL-2; but RPE cells do not inhibit the PHA-induced expression of early activation markers CD69, MHC class I and II, and of cyclin D of the PBLs. CONCLUSIONS: These results are the first to indicate that RPE cells impede generation of activated T cells by interfering with the induction of high-affinity IL-2R-alphabetagamma, IL-2 production, and the expression of CD71 and cyclin A.

AB - PURPOSE: To examine the effect of human retinal pigment epithelial (RPE) cells on phytohemagglutinin (PHA) activation of T cells. METHODS: Resting peripheral blood lymphocytes (PBLs) were stimulated with PHA with or without the presence of gamma-irradiated RPE cells. Proliferation and the cell cycle profile were thereafter investigated by 3H-thymidine incorporation and flow cytometric analysis. In addition, the PBLs expression of CD69, major histocompatibility complex (MHC) class I and II, CD3, as well as the IL-2 receptor chains were evaluated by flow cytometry, and the content of IL-2 in cell culture supernatant was measured by ELISA. RESULTS: Human RPE cells were found to suppress PHA-induced proliferation, cyclin A, IL-2R-alpha and -gamma, and CD71 expression and decrease the production of IL-2; but RPE cells do not inhibit the PHA-induced expression of early activation markers CD69, MHC class I and II, and of cyclin D of the PBLs. CONCLUSIONS: These results are the first to indicate that RPE cells impede generation of activated T cells by interfering with the induction of high-affinity IL-2R-alphabetagamma, IL-2 production, and the expression of CD71 and cyclin A.

U2 - 10.1080/02713680590934120

DO - 10.1080/02713680590934120

M3 - Journal article

C2 - 16020268

VL - 30

SP - 375

EP - 383

JO - Current Eye Research

JF - Current Eye Research

SN - 0271-3683

IS - 5

ER -

ID: 8724898