Evidence has been accumulating that shows that insulin-dependent diabetes is subject to immunoregulation. To determine whether cytotoxic T lymphocyte–associated antigen 4 (CTLA-4) is involved, we injected anti–CTLA-4 mAb into a TCR transgenic model of diabetes at different stages of disease. When injected into young mice, months before they would normally become diabetic, anti–CTLA-4 induced diabetes rapidly and essentially universally; this was not the result of a global activation of T lymphocytes, but did reflect a much more aggressive T cell infiltrate in the pancreatic islets. These effects were only observed if anti–CTLA-4 was injected during a narrow time window, before the initiation of insulitis. Thus, engagement of CTLA-4 at the time when potentially diabetogenic T cells are first activated is a pivotal event; if engagement is permitted, invasion of the islets occurs, but remains quite innocuous for months, if not, insulitis is much more aggressive, and diabetes quickly ensues.
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2 February 1998
Brief Definitive Report|
February 02 1998
Cytotoxic T Lymphocyte–associated Antigen 4 (CTLA-4) Regulates the Unfolding of Autoimmune Diabetes
Fred Lühder,
Fred Lühder
From the *Institut de Génétique et de Biologie Moléculaire et Cellulaire (CNRS/INSERM/ULP), 1 rue Laurent Fries, 67404 Illkirch, Communanté Urbain de Strasbourg, France; and the ‡Howard Hughes Medical Institute, Cancer Research Laboratory, University of California, Berkeley, California 94720-0001
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Petter Höglund,
Petter Höglund
From the *Institut de Génétique et de Biologie Moléculaire et Cellulaire (CNRS/INSERM/ULP), 1 rue Laurent Fries, 67404 Illkirch, Communanté Urbain de Strasbourg, France; and the ‡Howard Hughes Medical Institute, Cancer Research Laboratory, University of California, Berkeley, California 94720-0001
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James P. Allison,
James P. Allison
From the *Institut de Génétique et de Biologie Moléculaire et Cellulaire (CNRS/INSERM/ULP), 1 rue Laurent Fries, 67404 Illkirch, Communanté Urbain de Strasbourg, France; and the ‡Howard Hughes Medical Institute, Cancer Research Laboratory, University of California, Berkeley, California 94720-0001
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Christophe Benoist,
Christophe Benoist
From the *Institut de Génétique et de Biologie Moléculaire et Cellulaire (CNRS/INSERM/ULP), 1 rue Laurent Fries, 67404 Illkirch, Communanté Urbain de Strasbourg, France; and the ‡Howard Hughes Medical Institute, Cancer Research Laboratory, University of California, Berkeley, California 94720-0001
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Diane Mathis
Diane Mathis
From the *Institut de Génétique et de Biologie Moléculaire et Cellulaire (CNRS/INSERM/ULP), 1 rue Laurent Fries, 67404 Illkirch, Communanté Urbain de Strasbourg, France; and the ‡Howard Hughes Medical Institute, Cancer Research Laboratory, University of California, Berkeley, California 94720-0001
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Fred Lühder
From the *Institut de Génétique et de Biologie Moléculaire et Cellulaire (CNRS/INSERM/ULP), 1 rue Laurent Fries, 67404 Illkirch, Communanté Urbain de Strasbourg, France; and the ‡Howard Hughes Medical Institute, Cancer Research Laboratory, University of California, Berkeley, California 94720-0001
Petter Höglund
From the *Institut de Génétique et de Biologie Moléculaire et Cellulaire (CNRS/INSERM/ULP), 1 rue Laurent Fries, 67404 Illkirch, Communanté Urbain de Strasbourg, France; and the ‡Howard Hughes Medical Institute, Cancer Research Laboratory, University of California, Berkeley, California 94720-0001
James P. Allison
From the *Institut de Génétique et de Biologie Moléculaire et Cellulaire (CNRS/INSERM/ULP), 1 rue Laurent Fries, 67404 Illkirch, Communanté Urbain de Strasbourg, France; and the ‡Howard Hughes Medical Institute, Cancer Research Laboratory, University of California, Berkeley, California 94720-0001
Christophe Benoist
From the *Institut de Génétique et de Biologie Moléculaire et Cellulaire (CNRS/INSERM/ULP), 1 rue Laurent Fries, 67404 Illkirch, Communanté Urbain de Strasbourg, France; and the ‡Howard Hughes Medical Institute, Cancer Research Laboratory, University of California, Berkeley, California 94720-0001
Diane Mathis
From the *Institut de Génétique et de Biologie Moléculaire et Cellulaire (CNRS/INSERM/ULP), 1 rue Laurent Fries, 67404 Illkirch, Communanté Urbain de Strasbourg, France; and the ‡Howard Hughes Medical Institute, Cancer Research Laboratory, University of California, Berkeley, California 94720-0001
Address correspondence to Drs. Diane Mathis and Christophe Benoist, IGBMC, 1 rue Laurent Fries, BP 163, 67404 Illkirch Cedex France. Phone: 33-3-88-65-32-00; Fax: 33-3-88-65-32-46; E-mail: [email protected]
Received:
September 08 1997
Revision Received:
November 03 1997
Online ISSN: 1540-9538
Print ISSN: 0022-1007
1998
J Exp Med (1998) 187 (3): 427–432.
Article history
Received:
September 08 1997
Revision Received:
November 03 1997
Citation
Fred Lühder, Petter Höglund, James P. Allison, Christophe Benoist, Diane Mathis; Cytotoxic T Lymphocyte–associated Antigen 4 (CTLA-4) Regulates the Unfolding of Autoimmune Diabetes . J Exp Med 2 February 1998; 187 (3): 427–432. doi: https://doi.org/10.1084/jem.187.3.427
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