T cell hybridomas isolated from nonresponder H-2b mice immunized with pork insulin were stimulated by insulin in the presence of major histocompatibility complex (MHC)-unmatched antigen presenting cells. The restriction element used by these CD4− T cells was mapped to an oligomorphic MHC class Ib protein encoded in the T region and identified as Qa-1b using transfectants. The antigenic determinant was localized to the insulin B chain, and experiments with truncated peptides suggested that it is unexpectedly long, comprising most or all of the 30 amino acid B chain. The antigen processing pathway used to present insulin to the Qa-1b– restricted T cells does not require transporters associated with antigen processing (TAP), and it is inhibited by chloroquine. A wide variety of cell lines from different tissues efficiently present soluble insulin to Qa-1b–restricted T cells, and insulin presentation is not enhanced by phagocytic stimuli. Our results demonstrate that Qa-1b can function to present exogenous protein to T cells in a manner similar to MHC class II molecules. Therefore, this class Ib protein may have access to a novel antigen processing pathway that is not available to class Ia molecules.
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7 September 1998
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September 07 1998
Transporters Associated with Antigen Processing (TAP)-independent Presentation of Soluble Insulin to α/β T Cells by the Class Ib Gene Product, Qa-1b
S. Mark Tompkins,
S. Mark Tompkins
From the *Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia 30322; and the ‡Division of Molecular and Clinical Rheumatology, Department of Medicine, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205
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Jennifer R. Kraft,
Jennifer R. Kraft
From the *Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia 30322; and the ‡Division of Molecular and Clinical Rheumatology, Department of Medicine, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205
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Chinh T. Dao,
Chinh T. Dao
From the *Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia 30322; and the ‡Division of Molecular and Clinical Rheumatology, Department of Medicine, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205
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Mark J. Soloski,
Mark J. Soloski
From the *Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia 30322; and the ‡Division of Molecular and Clinical Rheumatology, Department of Medicine, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205
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Peter E. Jensen
Peter E. Jensen
From the *Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia 30322; and the ‡Division of Molecular and Clinical Rheumatology, Department of Medicine, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205
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S. Mark Tompkins
From the *Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia 30322; and the ‡Division of Molecular and Clinical Rheumatology, Department of Medicine, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205
Jennifer R. Kraft
From the *Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia 30322; and the ‡Division of Molecular and Clinical Rheumatology, Department of Medicine, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205
Chinh T. Dao
From the *Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia 30322; and the ‡Division of Molecular and Clinical Rheumatology, Department of Medicine, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205
Mark J. Soloski
From the *Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia 30322; and the ‡Division of Molecular and Clinical Rheumatology, Department of Medicine, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205
Peter E. Jensen
From the *Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia 30322; and the ‡Division of Molecular and Clinical Rheumatology, Department of Medicine, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205
Address correspondence to P.E. Jensen, Department of Pathology and Laboratory Medicine, Rm. 7309 WMB, Emory University School of Medicine, Atlanta, GA 30322. Phone: 404-727-3658; Fax: 404-727-5764; E-mail: [email protected]
Received:
May 19 1998
Online ISSN: 1540-9538
Print ISSN: 0022-1007
1998
J Exp Med (1998) 188 (5): 961–971.
Article history
Received:
May 19 1998
Citation
S. Mark Tompkins, Jennifer R. Kraft, Chinh T. Dao, Mark J. Soloski, Peter E. Jensen; Transporters Associated with Antigen Processing (TAP)-independent Presentation of Soluble Insulin to α/β T Cells by the Class Ib Gene Product, Qa-1b . J Exp Med 7 September 1998; 188 (5): 961–971. doi: https://doi.org/10.1084/jem.188.5.961
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