Human CD4+ T cells displaying viral epitopes elicit a functional virus-specific memory CD8+ T cell response.

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Human CD4+ T cells displaying viral epitopes elicit a functional virus-specific memory CD8+ T cell response. / Adamopoulou, Eleni; Diekmann, Jan; Tolosa, Eva; Kuntz, Gaby; Einsele, Hermann; Rammensee, Hans-Georg; Topp, Max S.

in: J IMMUNOL, Jahrgang 178, Nr. 9, 9, 2007, S. 5465-5472.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Adamopoulou, E, Diekmann, J, Tolosa, E, Kuntz, G, Einsele, H, Rammensee, H-G & Topp, MS 2007, 'Human CD4+ T cells displaying viral epitopes elicit a functional virus-specific memory CD8+ T cell response.', J IMMUNOL, Jg. 178, Nr. 9, 9, S. 5465-5472. <http://www.ncbi.nlm.nih.gov/pubmed/17442927?dopt=Citation>

APA

Vancouver

Adamopoulou E, Diekmann J, Tolosa E, Kuntz G, Einsele H, Rammensee H-G et al. Human CD4+ T cells displaying viral epitopes elicit a functional virus-specific memory CD8+ T cell response. J IMMUNOL. 2007;178(9):5465-5472. 9.

Bibtex

@article{6160b86007974d759ddc777500d0bd21,
title = "Human CD4+ T cells displaying viral epitopes elicit a functional virus-specific memory CD8+ T cell response.",
abstract = "The Ag-specific cellular recall response to herpes virus infections is characterized by a swift recruitment of virus-specific memory T cells. Rapid activation is achieved through formation of the immunological synapse and supramolecular clustering of signal molecules at the site of contact. During the formation of the immunological synapse, epitope-loaded MHC molecules are transferred via trogocytosis from APCs to T cells, enabling the latter to function as Ag-presenting T cells (T-APCs). The contribution of viral epitope expressing T-APCs in the regulation of the herpes virus-specific CD8+ T cell memory response remains unclear. Comparison of CD4+ T-APCs with professional APCs such as Ag-presenting CD40L-activated B cells (CD40B-APCs) demonstrated reduced levels of costimulatory ligands. Despite the observed differences, CD4+ T-APCs are as potent as CD40B-APCs in stimulating herpes virus-specific CD8+ T cells resulting in a greater than 35-fold expansion of CD8+ T cells specific for dominant and subdominant viral epitopes. Virus-specific CD8+ T cells generated by CD4+ T-APCs or CD40B-APCs showed both comparable effector function such as specific lysis of targets and cytokine production and also did not differ in their phenotype after expansion. These results indicate that viral epitope presentation by Ag-specific CD4+ T cells may contribute to the rapid recruitment of virus-specific memory CD8+ T cells during a viral recall response.",
keywords = "Humans, T-Lymphocytes, Cytotoxic/*immunology, B-Lymphocytes/immunology, Epitopes/genetics/*immunology, CD4-Positive T-Lymphocytes/*immunology, Antigen Presentation, Antigen-Presenting Cells/immunology, Antigens, CD8/analysis, Antigens, Viral/genetics/*immunology, Herpes Simplex/immunology, Immunologic Memory/*immunology, Simplexvirus/*immunology, Humans, T-Lymphocytes, Cytotoxic/*immunology, B-Lymphocytes/immunology, Epitopes/genetics/*immunology, CD4-Positive T-Lymphocytes/*immunology, Antigen Presentation, Antigen-Presenting Cells/immunology, Antigens, CD8/analysis, Antigens, Viral/genetics/*immunology, Herpes Simplex/immunology, Immunologic Memory/*immunology, Simplexvirus/*immunology",
author = "Eleni Adamopoulou and Jan Diekmann and Eva Tolosa and Gaby Kuntz and Hermann Einsele and Hans-Georg Rammensee and Topp, {Max S}",
year = "2007",
language = "English",
volume = "178",
pages = "5465--5472",
journal = "J IMMUNOL",
issn = "0022-1767",
publisher = "American Association of Immunologists",
number = "9",

}

RIS

TY - JOUR

T1 - Human CD4+ T cells displaying viral epitopes elicit a functional virus-specific memory CD8+ T cell response.

AU - Adamopoulou, Eleni

AU - Diekmann, Jan

AU - Tolosa, Eva

AU - Kuntz, Gaby

AU - Einsele, Hermann

AU - Rammensee, Hans-Georg

AU - Topp, Max S

PY - 2007

Y1 - 2007

N2 - The Ag-specific cellular recall response to herpes virus infections is characterized by a swift recruitment of virus-specific memory T cells. Rapid activation is achieved through formation of the immunological synapse and supramolecular clustering of signal molecules at the site of contact. During the formation of the immunological synapse, epitope-loaded MHC molecules are transferred via trogocytosis from APCs to T cells, enabling the latter to function as Ag-presenting T cells (T-APCs). The contribution of viral epitope expressing T-APCs in the regulation of the herpes virus-specific CD8+ T cell memory response remains unclear. Comparison of CD4+ T-APCs with professional APCs such as Ag-presenting CD40L-activated B cells (CD40B-APCs) demonstrated reduced levels of costimulatory ligands. Despite the observed differences, CD4+ T-APCs are as potent as CD40B-APCs in stimulating herpes virus-specific CD8+ T cells resulting in a greater than 35-fold expansion of CD8+ T cells specific for dominant and subdominant viral epitopes. Virus-specific CD8+ T cells generated by CD4+ T-APCs or CD40B-APCs showed both comparable effector function such as specific lysis of targets and cytokine production and also did not differ in their phenotype after expansion. These results indicate that viral epitope presentation by Ag-specific CD4+ T cells may contribute to the rapid recruitment of virus-specific memory CD8+ T cells during a viral recall response.

AB - The Ag-specific cellular recall response to herpes virus infections is characterized by a swift recruitment of virus-specific memory T cells. Rapid activation is achieved through formation of the immunological synapse and supramolecular clustering of signal molecules at the site of contact. During the formation of the immunological synapse, epitope-loaded MHC molecules are transferred via trogocytosis from APCs to T cells, enabling the latter to function as Ag-presenting T cells (T-APCs). The contribution of viral epitope expressing T-APCs in the regulation of the herpes virus-specific CD8+ T cell memory response remains unclear. Comparison of CD4+ T-APCs with professional APCs such as Ag-presenting CD40L-activated B cells (CD40B-APCs) demonstrated reduced levels of costimulatory ligands. Despite the observed differences, CD4+ T-APCs are as potent as CD40B-APCs in stimulating herpes virus-specific CD8+ T cells resulting in a greater than 35-fold expansion of CD8+ T cells specific for dominant and subdominant viral epitopes. Virus-specific CD8+ T cells generated by CD4+ T-APCs or CD40B-APCs showed both comparable effector function such as specific lysis of targets and cytokine production and also did not differ in their phenotype after expansion. These results indicate that viral epitope presentation by Ag-specific CD4+ T cells may contribute to the rapid recruitment of virus-specific memory CD8+ T cells during a viral recall response.

KW - Humans

KW - T-Lymphocytes, Cytotoxic/immunology

KW - B-Lymphocytes/immunology

KW - Epitopes/genetics/immunology

KW - CD4-Positive T-Lymphocytes/immunology

KW - Antigen Presentation

KW - Antigen-Presenting Cells/immunology

KW - Antigens, CD8/analysis

KW - Antigens, Viral/genetics/immunology

KW - Herpes Simplex/immunology

KW - Immunologic Memory/immunology

KW - Simplexvirus/immunology

KW - Humans

KW - T-Lymphocytes, Cytotoxic/immunology

KW - B-Lymphocytes/immunology

KW - Epitopes/genetics/immunology

KW - CD4-Positive T-Lymphocytes/immunology

KW - Antigen Presentation

KW - Antigen-Presenting Cells/immunology

KW - Antigens, CD8/analysis

KW - Antigens, Viral/genetics/immunology

KW - Herpes Simplex/immunology

KW - Immunologic Memory/immunology

KW - Simplexvirus/immunology

M3 - SCORING: Journal article

VL - 178

SP - 5465

EP - 5472

JO - J IMMUNOL

JF - J IMMUNOL

SN - 0022-1767

IS - 9

M1 - 9

ER -