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The Journal of Immunology, 1999, 162: 3153-3159.
Copyright © 1999 by The American Association of Immunologists

Reciprocal Expression in CD4 or CD8 Subsets of Different Members of the V{alpha}11 Gene Family Correlates with Sequence Polymorphism1

Bee-Cheng Sim and Nicholas R. J. Gascoigne2

Department of Immunology, The Scripps Research Institute, La Jolla, CA 92037

Previous staining studies with TCR V{alpha}11-specific mAbs showed that V{alpha}11.1/11.2 (AV11S1 and S2) expression was selectively favored in the CD4+ peripheral T cell population. As this phenomenon was essentially independent of the MHC haplotype, it was suggested that AV11S1 and S2 TCRs exert a preference for recognition of class II MHC molecules. The V{alpha} segment of the TCR {alpha}-chain is suggested to have a primary role in shaping the T cell repertoire due to selection for class I or II molecules acting through the complementarity determining regions (CDR) 1{alpha} and CDR2{alpha} residues. We have analyzed the repertoire of V{alpha}11 family members expressed in C57BL/6 mice and have identified a new member of this family; AV11S8. We show that, whereas AV11S1 and S2 are more frequent in CD4+ cells, AV11S3 and S8 are more frequent in CD8+ cells. The sequences in the CDR1{alpha} and CDR2{alpha} correlate with differential expression in CD4+ or CD8+ cells, a phenomenon that is also observed in BALB/c mice. With no apparent restriction in TCR J{alpha} usage or CDR3{alpha} length in C57BL/6, these findings support the idea of V{alpha}-dependent T cell repertoire selection through preferential recognition of MHC class I or class II molecules.




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