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Escape from CD8+ T cell response by natural variants of an immunodominant epitope from Theilaria parva is predominantly due to loss of TCR recognition

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)5910-5920
Number of pages11
JournalJournal of Immunology
Volume187
Publication statusPublished - Sep 2011

Abstract

Polymorphism of immunodominant CD8(+) T cell epitopes can facilitate escape from immune recognition of pathogens, leading to strain-specific immunity. In this study, we examined the TCR β-chain (TRB) diversity of the CD8(+) T cell responses of cattle against two immunodominant epitopes from Theileria parva (Tp1(214-224) and Tp2(49-59)) and investigated the role of TCR recognition and MHC binding in determining differential recognition of a series of natural variants of the highly polymorphic Tp2(49-59) epitope by CD8(+) T cell clones of defined TRB genotype. Our results show that both Tp1(214-224) and Tp2(49-59) elicited CD8(+) T cell responses using diverse TRB repertoires that showed a high level of stability following repeated pathogenic challenge over a 3-y period. Analysis of single-alanine substituted versions of the Tp2(49-59) peptide demonstrated that Tp2(49-59)-specific clonotypes had a broad range of fine specificities for the epitope. Despite this diversity, all natural variants exhibited partial or total escape from immune recognition, which was predominantly due to abrogation of TCR recognition, with mutation resulting in loss of the lysine residue at P8, playing a particularly dominant role in escape. The levels of heterozygosity in individual Tp2(49-59) residues correlated closely with loss of immune recognition, suggesting that immune selection has contributed to epitope polymorphism.

    Research areas

  • Animals, CD8-Positive T-Lymphocytes/immunology, Cattle, Epitopes, T-Lymphocyte/genetics, Epitopes, T-Lymphocyte/immunology, Immune Tolerance/genetics, Immune Tolerance/immunology, Immunodominant Epitopes/genetics, Immunodominant Epitopes/immunology, Lymphocyte Activation/immunology, Polymorphism, Genetic, Receptors, Antigen, T-Cell, alpha-beta/genetics, Receptors, Antigen, T-Cell, alpha-beta/immunology, Reverse Transcriptase Polymerase Chain Reaction, Theileria parva/genetics, Theileria parva/immunology, Theileriasis/genetics, Theileriasis/immunology

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