liu.seSearch for publications in DiVA
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • oxford
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Peripheral Follicular T Helper Cells and Mucosal-Associated Invariant T Cells Represent Activated Phenotypes During the Febrile Phase of Acute Dengue Virus Infection
Sch Life Sci, India.
Govt Theni Med Coll & Hosp, India.
Govt Theni Med Coll & Hosp, India.
Xiamen Univ Malaysia, Malaysia.
Show others and affiliations
2020 (English)In: Viral immunology, ISSN 0882-8245, E-ISSN 1557-8976, Vol. 33, no 9, p. 610-615Article in journal (Refereed) Published
Abstract [en]

Peripheral follicular helper T (pTfh) cells represent specialized CD4(+)T cells that help B cells to secrete antibodies. Dengue infection appears to cause immune activation in a wide array of immune cells. Herein, we investigated the signatures of immune activation of circulating Tfh cells and mucosal-associated invariant T (MAIT) cells in adult subjects with confirmed acute clinical dengue virus (DENV) infection by multiparametric flow cytometry. The acute DENV infection induced a significant expansion and activation of pTfh cells and circulating MAIT cells during acute febrile infection. We found a higher frequency of activated PD-1(+)Tfh cells and CD38(+)pTfh cells in clinical DENV infection. We also found similar activated and expanding phenotypes of MAIT cells in the patients tested. The numbers of activated pTfh cells and circulating MAIT cells were higher in dengue patients relative to healthy controls. We concluded that pTfh cells and circulating MAIT cells represent activated phenotypes in acute DENV infection.

Place, publisher, year, edition, pages
MARY ANN LIEBERT, INC , 2020. Vol. 33, no 9, p. 610-615
Keywords [en]
CD38; dengue virus; Ki67; MAIT cells; pTfh cells
National Category
Immunology in the medical area
Identifiers
URN: urn:nbn:se:liu:diva-171051DOI: 10.1089/vim.2020.0149ISI: 000575395300001PubMedID: 32996843OAI: oai:DiVA.org:liu-171051DiVA, id: diva2:1485211
Note

Funding Agencies|Department of Science and Technology-Science and Engineering Research Board, Government of India [CRG/2019/006096]; Swedish Research CouncilSwedish Research Council; Swedish Physicians Against AIDS Research Foundation; Swedish International Development Cooperation Agency; SIDA SARC; VINNMER for VinnovaVinnova; Linkoping University Hospital Research Fund; CALF; Swedish Society of Medicine; Xiamen University Malaysia Research Funding (XMUMRF) [XMUMRF/2018-C2/ILAB/0001, XMUMRF/2020-C5/ITCM/0003]; Department of Health Research, Ministry of Health and Family Welfare, Government of India [VIR/66/2013/ECD-I, R.12020/04/2018-HR]; [AI52731]

Available from: 2020-11-01 Created: 2020-11-01 Last updated: 2021-04-12

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMed

Search in DiVA

By author/editor
Larsson, Marie
By organisation
Division of Molecular Medicine and VirologyFaculty of Medicine and Health Sciences
In the same journal
Viral immunology
Immunology in the medical area

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 570 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • oxford
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf