Rats of the PVG.RT1u strain develop autoimmune diabetes when thymectomized at 6 wk of age and are rendered relatively lymphopenic by a cumulative dose of 1,000 rads 137Cs γ-irradiation given in four split doses. Previous studies have shown that the disease is prevented by the intravenous injection of 5 × 106 CD4+ CD45RC− TCRαβ+ RT6+ peripheral T cells from normal syngeneic donors. These cells have a memory phenotype and are presumably primed to some extrathymic antigen. However, we now report that the CD4+ CD8− population of mature thymocytes is a very potent source of cells, with the capacity to prevent diabetes in our lymphopenic animals. As few as 6 × 105 of these cells protect ∼50% of recipients and the level of protection increases with cell dose. It appears that one characteristic of the intrathymic selection of the T cell repertoire is the generation of cells that regulate the autoimmune potential of peripheral T cells that have been neither clonally deleted intrathymically nor rendered irreversibly anergic in the periphery.
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1 December 1996
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Brief Definitive Report|
December 01 1996
The Thymus Contains a High Frequency of Cells that Prevent Autoimmune Diabetes on Transfer into Prediabetic Recipients
Abdelhadi Saoudi,
Abdelhadi Saoudi
From the *Medical Research Council Cellular Immunology Unit, Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE United Kingdom; ‡Institute National de la Santé et de la Recherche Médicale U28, Hôpital Purpan, 31059, Toulouse, France; and §Infectious Disease Division, University of California, San Francisco, California 94143-0654
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Benedict Seddon,
Benedict Seddon
From the *Medical Research Council Cellular Immunology Unit, Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE United Kingdom; ‡Institute National de la Santé et de la Recherche Médicale U28, Hôpital Purpan, 31059, Toulouse, France; and §Infectious Disease Division, University of California, San Francisco, California 94143-0654
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Debbie Fowell,
Debbie Fowell
From the *Medical Research Council Cellular Immunology Unit, Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE United Kingdom; ‡Institute National de la Santé et de la Recherche Médicale U28, Hôpital Purpan, 31059, Toulouse, France; and §Infectious Disease Division, University of California, San Francisco, California 94143-0654
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Don Mason
Don Mason
From the *Medical Research Council Cellular Immunology Unit, Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE United Kingdom; ‡Institute National de la Santé et de la Recherche Médicale U28, Hôpital Purpan, 31059, Toulouse, France; and §Infectious Disease Division, University of California, San Francisco, California 94143-0654
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Abdelhadi Saoudi
,
Benedict Seddon
,
Debbie Fowell
,
Don Mason
From the *Medical Research Council Cellular Immunology Unit, Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE United Kingdom; ‡Institute National de la Santé et de la Recherche Médicale U28, Hôpital Purpan, 31059, Toulouse, France; and §Infectious Disease Division, University of California, San Francisco, California 94143-0654
Address correspondence to Ben Seddon, MRC Cellular Immunology Unit, Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, UK.
A. Saoudi is supported by a postdoctoral fellowship from the Wellcome Trust and from the Fondation pour la Recherche Medicale of France. B. Seddon is supported by a Wellcome Trust Prize Studentship.
A. Saoudi and B. Seddon contributed equally to this work.
Received:
July 08 1996
Revision Received:
September 23 1996
Online ISSN: 1540-9538
Print ISSN: 0022-1007
1996
J Exp Med (1996) 184 (6): 2393–2398.
Article history
Received:
July 08 1996
Revision Received:
September 23 1996
Citation
Abdelhadi Saoudi, Benedict Seddon, Debbie Fowell, Don Mason; The Thymus Contains a High Frequency of Cells that Prevent Autoimmune Diabetes on Transfer into Prediabetic Recipients. J Exp Med 1 December 1996; 184 (6): 2393–2398. doi: https://doi.org/10.1084/jem.184.6.2393
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