Selective retention of virus-specific tissue-resident T cells in healed skin after recovery from herpes zoster
Kerry J. Laing (),
Werner J. D. Ouwendijk,
Victoria L. Campbell,
Christopher L. McClurkan,
Shahin Mortazavi,
Michael Elder Waters,
Maxwell P. Krist,
Richard Tu,
Nhi Nguyen,
Krithi Basu,
Congrong Miao,
D. Scott Schmid,
Christine Johnston,
Georges M. G. M. Verjans and
David M. Koelle
Additional contact information
Kerry J. Laing: University of Washington
Werner J. D. Ouwendijk: Erasmus Medical Center
Victoria L. Campbell: University of Washington
Christopher L. McClurkan: University of Washington
Shahin Mortazavi: University of Washington
Michael Elder Waters: University of Washington
Maxwell P. Krist: University of Washington
Richard Tu: University of Washington
Nhi Nguyen: University of Washington
Krithi Basu: University of Washington
Congrong Miao: Division of Viral Diseases
D. Scott Schmid: Division of Viral Diseases
Christine Johnston: University of Washington
Georges M. G. M. Verjans: Erasmus Medical Center
David M. Koelle: University of Washington
Nature Communications, 2022, vol. 13, issue 1, 1-13
Abstract:
Abstract Herpes zoster is a localized skin infection caused by reactivation of latent varicella-zoster virus. Tissue-resident T cells likely control skin infections. Zoster provides a unique opportunity to determine if focal reinfection of human skin boosts local or disseminated antigen-specific tissue-resident T cells. Here, we show virus-specific T cells are retained over one year in serial samples of rash site and contralateral unaffected skin of individuals recovered from zoster. Consistent with zoster resolution, viral DNA is largely undetectable on skin from day 90 and virus-specific B and T cells decline in blood. In skin, there is selective infiltration and long-term persistence of varicella-zoster virus-specific T cells in the rash site relative to the contralateral site. The skin T cell infiltrates express the canonical tissue-resident T cell markers CD69 and CD103. These findings show that zoster promotes spatially-restricted long-term retention of antigen-specific tissue-resident T cells in previously infected skin.
Date: 2022
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-34698-4
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DOI: 10.1038/s41467-022-34698-4
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