[125I](T,G)-A--L-binding T cells have been studied in mice whose ability to mount an immune response to (T,G)-A--L is under control of the H-2-linked Ir-1A gene. Nonimmunized high and low responder mice have approximately the same frequency of T-ABC. Following immunization, T-ABC proliferated only in high responders, but not in low responders, indicating expression of Ir-1A in T cells. When, for comparison, [125I]arsanyl-mouse serum albumin binding B and T cells were investigated in mice whose antibody response to the hapten arsanyl is controlled by an allotype-linked Ir gene, it was found that following immunization the number of B-ABC increased only in high responders. In contrast, T-ABC proliferated to the same extent in both high and low responders, suggesting exclusive expression of the allotype-linked Ir gene in the B-cell line. Preliminary studies indicate that anti-Ia sera inhibit neither B-ABC nor T-ABC.
Article|
November 01 1974
COMPARATIVE ANALYSIS OF ANTIGEN-BINDING T CELLS IN GENETIC HIGH AND LOW RESPONDER MICE
Günter J. Hämmerling,
Günter J. Hämmerling
From the Division of Immunology, Department of Medicine, Stanford University School of Medicine, Stanford, California 94305
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Hugh O. McDevitt
Hugh O. McDevitt
From the Division of Immunology, Department of Medicine, Stanford University School of Medicine, Stanford, California 94305
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Günter J. Hämmerling
From the Division of Immunology, Department of Medicine, Stanford University School of Medicine, Stanford, California 94305
Hugh O. McDevitt
From the Division of Immunology, Department of Medicine, Stanford University School of Medicine, Stanford, California 94305
Received:
July 15 1974
Online Issn: 1540-9538
Print Issn: 0022-1007
Copyright © 1974 by The Rockefeller University Press
1974
J Exp Med (1974) 140 (5): 1180–1188.
Article history
Received:
July 15 1974
Citation
Günter J. Hämmerling, Hugh O. McDevitt; COMPARATIVE ANALYSIS OF ANTIGEN-BINDING T CELLS IN GENETIC HIGH AND LOW RESPONDER MICE . J Exp Med 1 November 1974; 140 (5): 1180–1188. doi: https://doi.org/10.1084/jem.140.5.1180
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