Major Histocompatibility Complex Class I Allele-specific Cooperative and Competitive Interactions between Immune Evasion Proteins of Cytomegalovirus
Open Access
- 16 September 2002
- journal article
- Published by Rockefeller University Press in The Journal of Experimental Medicine
- Vol. 196 (6) , 805-816
- https://doi.org/10.1084/jem.20020811
Abstract
Cytomegaloviruses (CMVs) deploy a set of genes for interference with antigen presentation in the major histocompatibility complex (MHC) class I pathway. In murine CMV (MCMV), three genes were identified so far: m04/gp34, m06/gp48, and m152/gp40. While their function as immunoevasins was originally defined after their selective expression, this may not necessarily reflect their biological role during infection. The three immunoevasins might act synergistically, but they might also compete for their common substrate, the MHC class I complexes. To approach this question in a systematic manner, we have generated a complete set of mutant viruses with deletions of the three genes in all seven possible combinations. Surface expression of a set of MHC class I molecules specified by haplotypes H-2d (Kd, Dd, and Ld) and H-2b (Kb and Db) was the parameter for evaluation of the interference with class I trafficking. The data show the following: first, there exists no additional MCMV gene of major influence on MHC class I surface expression; second, the strength of the inhibitory effect of immunoevasins shows an allele-specific hierarchy; and third, the immunoevasins act not only synergistically but can, in certain combinations, interact antagonistically. In essence, this work highlights the importance of studying the immunosubversive mechanisms of cytomegaloviruses in the context of gene expression during the viral replicative cycle in infected cells.Keywords
This publication has 80 references indexed in Scilit:
- The Glycoprotein gp48 of Murine CytomegalovirusPublished by Elsevier ,2002
- Techniques: Recombinogenic engineering–new options for cloning and manipulating DNATrends in Biochemical Sciences, 2001
- Molecular Cloning of the Guinea Pig Cytomegalovirus (GPCMV) Genome as an Infectious Bacterial Artificial Chromosome (BAC) in Escherichia coliMolecular Genetics and Metabolism, 2001
- Viral Subversion of the Immune SystemAnnual Review of Immunology, 2000
- The Human Cytomegalovirus US11 Gene Product Dislocates MHC Class I Heavy Chains from the Endoplasmic Reticulum to the CytosolCell, 1996
- Gene disruption in Escherichia coli: TcR and KmR cassettes with the option of Flp-catalyzed excision of the antibiotic-resistance determinantGene, 1995
- Efficient processing of an antigenic sequence for presentation by MHC class I molecules depends on its neighboring residues in the proteinCell, 1991
- Cooperative interaction of B lymphocytes with antigen-specific helper T lymphocytes is MHC restrictedNature, 1981
- Fine Specificity Analysis with Monoclonal Antibodies of Antigens Controlled by the Major Histocompatibility Complex and by the Qa/TL Region in MiceImmunological Reviews, 1979
- Cell-mediated cytotoxicity to SV40-specific tumour-associated antigensNature, 1976