scholarly journals HLA-restricted epitope identification and detection of functional T cell responses by using MHC-peptide and costimulatory microarrays

2005 ◽  
Vol 102 (10) ◽  
pp. 3744-3749 ◽  
Author(s):  
J. D. Stone ◽  
W. E. Demkowicz ◽  
L. J. Stern
2011 ◽  
Vol 79 (5) ◽  
pp. 2059-2069 ◽  
Author(s):  
Niall D. MacHugh ◽  
William Weir ◽  
Alison Burrells ◽  
Regina Lizundia ◽  
Simon P. Graham ◽  
...  

ABSTRACTAlthough parasite strain-restricted CD8 T cell responses have been described for several protozoa, the precise role of antigenic variability in immunity is poorly understood. The tick-borne protozoan parasiteTheileria annulatainfects leukocytes and causes an acute, often fatal lymphoproliferative disease in cattle. Building on previous evidence of strain-restricted CD8 T cell responses toT. annulata, this study set out to identify and characterize the variability of the target antigens. Three antigens were identified by screening expressed parasite cDNAs with specific CD8 T cell lines. In cattle expressing the A10 class I major histocompatibility complex haplotype, A10-restricted CD8 T cell responses were shown to be focused entirely on a single dominant epitope in one of these antigens (Ta9). Sequencing of the Ta9 gene from field isolates ofT. annulatademonstrated extensive sequence divergence, resulting in amino acid polymorphism within the A10-restricted epitope and a second A14-restricted epitope. Statistical analysis of the allelic sequences revealed evidence of positive selection for amino acid substitutions within the region encoding the CD8 T cell epitopes. Sequence differences in the A10-restricted epitope were shown to result in differential recognition by individual CD8 T cell clones, while clones also differed in their ability to recognize different alleles. Moreover, the representation of these clonal specificities within the responding CD8 T cell populations differed between animals. As well as providing an explanation for incomplete protection observed after heterologous parasite challenge of vaccinated cattle, these results have important implications for the choice of antigens for the development of novel subunit vaccines.


2002 ◽  
Vol 168 (11) ◽  
pp. 5959-5965 ◽  
Author(s):  
Iva Zivna ◽  
Sharone Green ◽  
David W. Vaughn ◽  
Siripen Kalayanarooj ◽  
Henry A. F. Stephens ◽  
...  

Vaccine ◽  
2011 ◽  
Vol 29 (16) ◽  
pp. 3021-3030 ◽  
Author(s):  
Chantale Bernatchez ◽  
Kuichin Zhu ◽  
Yufeng Li ◽  
Helen Andersson ◽  
Constantin Ionnides ◽  
...  

2003 ◽  
Vol 170 (5) ◽  
pp. 2719-2726 ◽  
Author(s):  
Carmen Gianfrani ◽  
Riccardo Troncone ◽  
Patrizia Mugione ◽  
Elena Cosentini ◽  
Mariateresa De Pascale ◽  
...  

2001 ◽  
Vol 84 (8) ◽  
pp. 1052-1057 ◽  
Author(s):  
Y Umano ◽  
T Tsunoda ◽  
H Tanaka ◽  
K Matsuda ◽  
H Yamaue ◽  
...  

2002 ◽  
Vol 76 (22) ◽  
pp. 11780-11784 ◽  
Author(s):  
Bong-Su Kang ◽  
Michael A. Lyman ◽  
Byung S. Kim

ABSTRACT Theiler's murine encephalomyelitis virus (TMEV) infection induces immune-mediated demyelinating disease in susceptible mouse strains and serves as a relevant infectious model for human multiple sclerosis. To investigate the pathogenic mechanisms, two strains of TMEV (DA and BeAn), capable of inducing chronic demyelination in the central nervous system (CNS), have primarily been used. Here, we have compared the T-cell responses induced after infection with DA and BeAn strains in highly susceptible SJL/J mice. CD4+ T-cell responses to known epitopes induced by these two strains were virtually identical. However, the CD8+ T-cell response induced following DA infection in susceptible SJL/J mice was unable to recognize two of three H-2Ks-restricted epitope regions of BeAn, due to single-amino-acid substitutions. Interestingly, T cells specific for the H-2Ks-restricted epitope (VP111-20) recognized by both strains showed a drastic increase in frequency as well as avidity after infection with DA virus. These results strongly suggest that the level and avidity of virus-specific CD8+ T cells infiltrating the CNS could be drastically different after infection with these two strains of TMEV and may differentially influence the pathogenic and/or protective outcome.


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