Norovirus-specific CD8+ T cell responses in human blood and tissues

Abstract: Background & Aims
Noroviruses (NoVs) are the leading cause of acute gastroenteritis worldwide and are associated with significant morbidity and mortality. Moreover, an asymptomatic carrier state can persist following acute infection, promoting NoV spread and evolution. Thus, defining immune correlates of NoV protection and persistence is needed to guide the development of future vaccines and limit viral spread. Whereas antibody responses following NoV infection or vaccination have been studied extensively, cellular immunity has received less attention. Data from the mouse NoV model suggest that T cells are critical for preventing persistence and achieving viral clearance, but little is known about NoV-specific T-cell immunity in humans, particularly at mucosal sites.

Methods
We screened peripheral blood mononuclear cells from 3 volunteers with an overlapping NoV peptide library. We then used HLA-peptide tetramers to track virus-specific CD8+ T cells in peripheral, lymphoid, and intestinal tissues. Tetramer+ cells were further characterized using markers for cellular trafficking, exhaustion, cytotoxicity, and proliferation.

Results
We defined 7 HLA-restricted immunodominant class I epitopes that were highly conserved across pandemic strains from genogroup II.4. NoV-specific CD8+ T cells with central, effector, or tissue-resident memory phenotypes were present at all sites and were especially abundant in the intestinal lamina propria. The properties and differentiation states of tetramer+ cells varied across donors and epitopes.

Conclusions
Our findings are an important step toward defining the breadth, distribution, and properties of human NoV T-cell immunity. Moreover, the molecular tools we have developed can be used to evaluate future vaccines and engineer novel cellular therapeutics

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch
Notes
Cellular and Molecular Gastroenterology and Hepatology. - 11, 5 (2021) , 1267-1289, ISSN: 2352-345X

Event
Veröffentlichung
(where)
Freiburg
(who)
Universität
(when)
2021
Creator
Pattekar, Ajinkya
Mayer, Lena Sophie
Lau, Chi Wai
Liu, Chengyang
Palko, Olesya
Bewtra, Meenakshi
Human Pancreas Analysis Program, [Study Group]
Lindesmith, Lisa C.
Brewer-Jensen, Paul D.
Baric, Ralph S.
Betts, Michael R.
Naji, Ali
Wherry, E. John
Tomov, Vesselin T.

DOI
10.1016/j.jcmgh.2020.12.012
URN
urn:nbn:de:bsz:25-freidok-1940382
Rights
Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
25.03.2025, 1:41 PM CET

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Associated

  • Pattekar, Ajinkya
  • Mayer, Lena Sophie
  • Lau, Chi Wai
  • Liu, Chengyang
  • Palko, Olesya
  • Bewtra, Meenakshi
  • Human Pancreas Analysis Program, [Study Group]
  • Lindesmith, Lisa C.
  • Brewer-Jensen, Paul D.
  • Baric, Ralph S.
  • Betts, Michael R.
  • Naji, Ali
  • Wherry, E. John
  • Tomov, Vesselin T.
  • Universität

Time of origin

  • 2021

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