tetano
Editor, Senior Moderator
Sci Rep. 2016 Sep 15;6:33334. doi: 10.1038/srep33334.
[h=1]Long-term adaptation of the influenza A virus by escaping cytotoxic T-cell recognition.[/h] Woolthuis RG[SUP]1,[/SUP][SUP]2[/SUP], van Dorp CH[SUP]1,[/SUP][SUP]2[/SUP], Keşmir C[SUP]1[/SUP], de Boer RJ[SUP]1[/SUP], van Boven M[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] The evolutionary adaptation of the influenza A virus (IAV) to human antibodies is well characterised. Much less is known about the long-term evolution of cytotoxic T lymphocyte (CTL) epitopes, which are important antigens for clearance of infection. We construct an antigenic map of IAVs of all human subtypes using a compendium of 142 confirmed CTL epitopes, and show that IAV evolved gradually in the period 1932-2015, with infrequent antigenic jumps in the H3N2 subtype. Intriguingly, the number of CTL epitopes per virus decreases with more than one epitope per three years in the H3N2 subtype (from 84 epitopes per virus in 1968 to 64 in 2015), mostly attributed to the loss of HLA-B epitopes. We confirm these observations with epitope predictions. Our findings indicate that selection pressures imposed by CTL immunity shape the long-term evolution of IAV.
PMID: 27629812 DOI: 10.1038/srep33334
[PubMed - in process] Free full text
[h=1]Long-term adaptation of the influenza A virus by escaping cytotoxic T-cell recognition.[/h] Woolthuis RG[SUP]1,[/SUP][SUP]2[/SUP], van Dorp CH[SUP]1,[/SUP][SUP]2[/SUP], Keşmir C[SUP]1[/SUP], de Boer RJ[SUP]1[/SUP], van Boven M[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] The evolutionary adaptation of the influenza A virus (IAV) to human antibodies is well characterised. Much less is known about the long-term evolution of cytotoxic T lymphocyte (CTL) epitopes, which are important antigens for clearance of infection. We construct an antigenic map of IAVs of all human subtypes using a compendium of 142 confirmed CTL epitopes, and show that IAV evolved gradually in the period 1932-2015, with infrequent antigenic jumps in the H3N2 subtype. Intriguingly, the number of CTL epitopes per virus decreases with more than one epitope per three years in the H3N2 subtype (from 84 epitopes per virus in 1968 to 64 in 2015), mostly attributed to the loss of HLA-B epitopes. We confirm these observations with epitope predictions. Our findings indicate that selection pressures imposed by CTL immunity shape the long-term evolution of IAV.
PMID: 27629812 DOI: 10.1038/srep33334
[PubMed - in process] Free full text