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Department of Immunology, Faculty of Medicine, Imperial College of Science, Technology and Medicine, London, United Kingdom
Mammalian cells express up to six different MHC class I alleles, many of which differ in terms of their interaction with components of the Ag presentation pathway and level of cell surface expression. However, it is often assumed in Ag presentation studies that class I alleles function independently of each other. We have compared cell surface expression levels and function of MHC class I molecules in F1 hybrid mice with those in the homozygous parental strains. The level of cell surface expression of certain alleles in F1 mice differed significantly from 50% of that found on the same cell type in the corresponding parental strain, suggesting allele-specific competition for cell surface expression, and not expression solely according to gene dosage. The strongest effect was observed in H-2b x H-2k F1 mice, in which the H-2b class I molecules dominated over the H-2k class I molecules. The magnitude of H-2k-restricted CTL responses to influenza A virus infection was similar in the F1 hybrid and parental H-2k mice. However, in H-2k mice expressing a Kb transgene, cell surface levels of the endogenous class I molecules were down-regulated to a greater degree than in F1 hybrid mice, and H-2k-restricted CTL responses against influenza A virus were greatly reduced, although the CTL repertoire was apparently present. Therefore, certain MHC class I molecules compete with each other for cell surface expression, and the resulting low cell surface expression of specific alleles can lead to a severe reduction in the ability to generate a CTL response.
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