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Hemagglutinin Protein Is a Primary Target of the Measles Virus–Specific HLA‐A2–Restricted CD8+T Cell Response during Measles and after Vaccination
Author(s) -
Martin O. C. Ota,
Zaza M. Ndhlovu,
SangKon Oh,
Sucheep Piyasirisilp,
Jay A. Berzofsky,
William J. Moss,
Diane E. Griffin
Publication year - 2007
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/518006
Subject(s) - measles virus , virology , epitope , morbillivirus , paramyxoviridae , biology , measles , cd8 , antibody , hemagglutinin (influenza) , vaccination , antigen , immunology , rubella , t cell , virus , immune system , viral disease
To characterize the measles virus (MV)-specific T cell responses important for evaluation of measles vaccines, human leukocyte antigen (HLA)-A2-positive and -negative adults immunized with measles-mumps-rubella vaccine were studied. Both groups developed increases in antibody and in interferon (IFN)- gamma -producing cells in response to pooled hemagglutinin (H) and fusion peptides. HLA-A2-binding peptides were predicted for all MV-encoded proteins and confirmed by T2 cell stabilization. Twenty-nine peptides were tested, and 19 (6 from H) stimulated increased IFN- gamma secretion in a majority of vaccinees. Peptide-loaded HLA-A2 tetramers or immunoglobulin dimers documented MV-specific CD8+ T cell responses after vaccination and during measles and confirmed new A2 epitopes in H (250-259 and 516-525 aa) and matrix (M; 50-58 aa) protein and previously described epitopes in H (30-38 aa), M (211-219 aa), and nonstructural protein C (84-92 aa). No single peptide dominated the response. We conclude that H is an important stimulus for CD8+ T cell as well as for antibody responses in HLA-A2-positive individuals.

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