Deletion of autospecific T cells in T cell receptor (TCR) transgenic mice spares cells with normal TCR levels and low levels of CD8 molecules.

Hung‐Sia Teh(Institute of Molecular and Clinical Ophthalmology Basel), Hiroyuki Kishi(Institute of Molecular and Clinical Ophthalmology Basel), B Scott(Institute of Molecular and Clinical Ophthalmology Basel), Harald von Boehmer(Institute of Molecular and Clinical Ophthalmology Basel)
The Journal of Experimental Medicine
March 1, 1989
Cited by 224Open Access
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Abstract

Transgenic mice that carry on a large fraction of their T cells an alpha/beta T cell receptor that recognizes the male antigen in the context of H-2Db molecules were constructed. An mAb specific for the transgenic receptor was developed and used to analyze T cell subsets in male transgenic H-2b mice. The vast majority of immature CD4+8+ T cells that express the transgenic TCR were deleted in the male transgenic mouse. Nevertheless, the majority of T cells spared by this deletion process expressed a high level of the transgenic TCR. These T cells, however, had an abnormal CD4/CD8 phenotype in that they expressed either no CD8 molecules or only low levels.


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