Research Highlights | Nature Immunology

Research Highlights | Nature Immunology

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Access through your institution Buy or subscribe The efficacy of vaccination can be impaired considerably by even a mild coinfection; many and often conflicting reasons have been proposed for this phenomenon. Welsh and colleagues, in the _Journal of Virology_, use mice transgenic for a T cell antigen receptor specific for the male HY antigen or for virus peptide to determine how viral coinfection perturbs responses. Simultaneous triggering of HY- and virus-specific T cells results in robust responses by both populations; however, if the stimulation of HY-specific T cells is delayed by a few days, the responses to this antigen are lower. The possibility of activation-induced cell death or active killing by death receptors is ruled out; instead, the impairment coincides with the peak of virus-induced type I interferon (IFN-α or IFN-β). Indeed, interferon stimulators such as poly(I:C) also impair the response of bystander HY-specific T cells much like viral infection, but not if the cells lack the receptor for type I interferon. These findings have important implications for the effective generation of vaccine and memory responses. _ZF_ _J. Virol._ (6 April 2011) doi:10.1128/JVI.02516-10 This is a preview of subscription content, access via your institution ACCESS OPTIONS Access through your institution Subscribe to this journal Receive 12 print issues and online access $209.00 per year only $17.42 per issue Learn more Buy this article * Purchase on SpringerLink * Instant access to full article PDF Buy now Prices may be subject to local taxes which are calculated during checkout ADDITIONAL ACCESS OPTIONS: * Log in * Learn about institutional subscriptions * Read our FAQs * Contact customer support RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Research Highlights. _Nat Immunol_ 12, 518 (2011). https://doi.org/10.1038/ni0611-518 Download citation * Published: 18 May 2011 * Issue Date: June 2011 * DOI: https://doi.org/10.1038/ni0611-518 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative

Access through your institution Buy or subscribe The efficacy of vaccination can be impaired considerably by even a mild coinfection; many and often conflicting reasons have been proposed


for this phenomenon. Welsh and colleagues, in the _Journal of Virology_, use mice transgenic for a T cell antigen receptor specific for the male HY antigen or for virus peptide to determine


how viral coinfection perturbs responses. Simultaneous triggering of HY- and virus-specific T cells results in robust responses by both populations; however, if the stimulation of


HY-specific T cells is delayed by a few days, the responses to this antigen are lower. The possibility of activation-induced cell death or active killing by death receptors is ruled out;


instead, the impairment coincides with the peak of virus-induced type I interferon (IFN-α or IFN-β). Indeed, interferon stimulators such as poly(I:C) also impair the response of bystander


HY-specific T cells much like viral infection, but not if the cells lack the receptor for type I interferon. These findings have important implications for the effective generation of


vaccine and memory responses. _ZF_ _J. Virol._ (6 April 2011) doi:10.1128/JVI.02516-10 This is a preview of subscription content, access via your institution ACCESS OPTIONS Access through


your institution Subscribe to this journal Receive 12 print issues and online access $209.00 per year only $17.42 per issue Learn more Buy this article * Purchase on SpringerLink * Instant


access to full article PDF Buy now Prices may be subject to local taxes which are calculated during checkout ADDITIONAL ACCESS OPTIONS: * Log in * Learn about institutional subscriptions *


Read our FAQs * Contact customer support RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Research Highlights. _Nat Immunol_ 12, 518 (2011).


https://doi.org/10.1038/ni0611-518 Download citation * Published: 18 May 2011 * Issue Date: June 2011 * DOI: https://doi.org/10.1038/ni0611-518 SHARE THIS ARTICLE Anyone you share the


following link with will be able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer


Nature SharedIt content-sharing initiative