The behavior of antigen-specific CD4+ T lymphocytes during initial exposure to antigen probably influences their decision to become primed or tolerized, but this has not been examined directly in vivo. We have therefore tracked such cells in real time, in situ during the induction of oral priming versus oral tolerance. There were marked contrasts with respect to rate and type of movement and clustering between naive T cells and those exposed to antigen in immunogenic or tolerogenic forms. However, the major difference when comparing tolerized and primed T cells was that the latter formed larger and longer-lived clusters within mucosal and peripheral lymph nodes. This is the first comparison of the behavior of antigen-specific CD4+ T cells in situ in mucosal and systemic lymphoid tissues during the induction of priming versus tolerance in a physiologically relevant model in vivo.
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6 June 2005
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May 31 2005
In situ characterization of CD4+ T cell behavior in mucosal and systemic lymphoid tissues during the induction of oral priming and tolerance
Bernd H. Zinselmeyer,
Bernd H. Zinselmeyer
1Division of Immunology, Infection, and Inflammation, University of Glasgow, Western Infirmary, Glasgow G11 6NT, Scotland, UK
2Centre for Biophotonics, University of Strathclyde, Glasgow G4 0NR, Scotland, UK
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John Dempster,
John Dempster
3Department of Physiology and Pharmacology, University of Strathclyde, Glasgow G4 0NR, Scotland, UK
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Alison M. Gurney,
Alison M. Gurney
2Centre for Biophotonics, University of Strathclyde, Glasgow G4 0NR, Scotland, UK
3Department of Physiology and Pharmacology, University of Strathclyde, Glasgow G4 0NR, Scotland, UK
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David Wokosin,
David Wokosin
2Centre for Biophotonics, University of Strathclyde, Glasgow G4 0NR, Scotland, UK
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Mark Miller,
Mark Miller
4Department of Physiology and Biophysics, University of California, Irvine, CA 92697
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Hsiang Ho,
Hsiang Ho
4Department of Physiology and Biophysics, University of California, Irvine, CA 92697
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Owain R. Millington,
Owain R. Millington
1Division of Immunology, Infection, and Inflammation, University of Glasgow, Western Infirmary, Glasgow G11 6NT, Scotland, UK
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Karen M. Smith,
Karen M. Smith
1Division of Immunology, Infection, and Inflammation, University of Glasgow, Western Infirmary, Glasgow G11 6NT, Scotland, UK
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Catherine M. Rush,
Catherine M. Rush
1Division of Immunology, Infection, and Inflammation, University of Glasgow, Western Infirmary, Glasgow G11 6NT, Scotland, UK
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Ian Parker,
Ian Parker
5Department of Neurobiology and Behavior, University of California, Irvine, CA 92697
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Michael Cahalan,
Michael Cahalan
4Department of Physiology and Biophysics, University of California, Irvine, CA 92697
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James M. Brewer,
James M. Brewer
1Division of Immunology, Infection, and Inflammation, University of Glasgow, Western Infirmary, Glasgow G11 6NT, Scotland, UK
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Paul Garside
Paul Garside
1Division of Immunology, Infection, and Inflammation, University of Glasgow, Western Infirmary, Glasgow G11 6NT, Scotland, UK
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Bernd H. Zinselmeyer
1Division of Immunology, Infection, and Inflammation, University of Glasgow, Western Infirmary, Glasgow G11 6NT, Scotland, UK
2Centre for Biophotonics, University of Strathclyde, Glasgow G4 0NR, Scotland, UK
John Dempster
3Department of Physiology and Pharmacology, University of Strathclyde, Glasgow G4 0NR, Scotland, UK
Alison M. Gurney
2Centre for Biophotonics, University of Strathclyde, Glasgow G4 0NR, Scotland, UK
3Department of Physiology and Pharmacology, University of Strathclyde, Glasgow G4 0NR, Scotland, UK
David Wokosin
2Centre for Biophotonics, University of Strathclyde, Glasgow G4 0NR, Scotland, UK
Mark Miller
4Department of Physiology and Biophysics, University of California, Irvine, CA 92697
Hsiang Ho
4Department of Physiology and Biophysics, University of California, Irvine, CA 92697
Owain R. Millington
1Division of Immunology, Infection, and Inflammation, University of Glasgow, Western Infirmary, Glasgow G11 6NT, Scotland, UK
Karen M. Smith
1Division of Immunology, Infection, and Inflammation, University of Glasgow, Western Infirmary, Glasgow G11 6NT, Scotland, UK
Catherine M. Rush
1Division of Immunology, Infection, and Inflammation, University of Glasgow, Western Infirmary, Glasgow G11 6NT, Scotland, UK
Ian Parker
5Department of Neurobiology and Behavior, University of California, Irvine, CA 92697
Michael Cahalan
4Department of Physiology and Biophysics, University of California, Irvine, CA 92697
James M. Brewer
1Division of Immunology, Infection, and Inflammation, University of Glasgow, Western Infirmary, Glasgow G11 6NT, Scotland, UK
Paul Garside
1Division of Immunology, Infection, and Inflammation, University of Glasgow, Western Infirmary, Glasgow G11 6NT, Scotland, UK
CORRESPONDENCE Paul Garside: [email protected] OR Michael Cahalan: [email protected]
Abbreviations used: CFSE, carboxyl fluorescein succinimidyl ester; CLN, cervical LN; CT, cholera toxin; MLN, mesenteric LN; PLN, peripheral LN; SMAC, supramolecular cluster; Tg, transgenic.
Received:
January 25 2005
Accepted:
April 19 2005
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2005
J Exp Med (2005) 201 (11): 1815–1823.
Article history
Received:
January 25 2005
Accepted:
April 19 2005
Citation
Bernd H. Zinselmeyer, John Dempster, Alison M. Gurney, David Wokosin, Mark Miller, Hsiang Ho, Owain R. Millington, Karen M. Smith, Catherine M. Rush, Ian Parker, Michael Cahalan, James M. Brewer, Paul Garside; In situ characterization of CD4+ T cell behavior in mucosal and systemic lymphoid tissues during the induction of oral priming and tolerance . J Exp Med 6 June 2005; 201 (11): 1815–1823. doi: https://doi.org/10.1084/jem.20050203
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