Modification of the HIV-specific CD8+ T-cell response in an HIV elite controller after chikungunya virus infection

AIDS ◽  
2016 ◽  
Vol 30 (12) ◽  
pp. 1905-1911 ◽  
Author(s):  
Yanina Ghiglione ◽  
María Julia Ruiz ◽  
Jimena Salido ◽  
César Trifone ◽  
Omar Sued ◽  
...  
2017 ◽  
Vol 21 (1) ◽  
pp. 35-46 ◽  
Author(s):  
Annie Elong Ngono ◽  
Edward A. Vizcarra ◽  
William W. Tang ◽  
Nicholas Sheets ◽  
Yunichel Joo ◽  
...  

2001 ◽  
Vol 166 (4) ◽  
pp. 2348-2356 ◽  
Author(s):  
David Masopust ◽  
Jiu Jiang ◽  
Hao Shen ◽  
Leo Lefrançois

Author(s):  
Yang Wang ◽  
Alexandra Tsitsiklis ◽  
Wei Gao ◽  
H. Hamlet Chu ◽  
Yan Zhang ◽  
...  

AbstractCertain CD8 T cell responses are particularly effective at controlling infection, as exemplified by elite control of HIV in individuals harboring HLA-B57. To understand the structural features that contribute to CD8 T cell elite control, we focused on a strongly protective CD8 T cell response directed against a parasite-derived peptide (HF10) presented by an atypical MHC-I molecule, H-2Ld. This response exhibits a focused TCR repertoire dominated by Vβ2, and a representative TCR (TG6) in complex with Ld-HF10 reveals an unusual structure in which both MHC and TCR contribute extensively to peptide specificity, along with a parallel footprint of TCR on its pMHC ligand. The parallel footprint is a common feature of Vβ2-containing TCRs and correlates with an unusual Vα-Vβ interface, CDR loop conformations, and Vβ2-specific germline contacts with peptide. Vβ2 and Ld may represent “specialist” components for antigen recognition that allow for particularly strong and focused T cell responses.


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