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Decrease of CD69 levels on TCR V7.2(+)CD4(+) innate-like lymphocytes is associated with impaired cytotoxic functions in chronic hepatitis B virus-infected patients
University of Malaya, Malaysia.
University of Malaya, Malaysia.
University of Malaya, Malaysia.
University of Malaya, Malaysia.
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2017 (Engelska)Ingår i: Innate Immunity, ISSN 1753-4259, E-ISSN 1753-4267, Vol. 23, nr 5, s. 459-467Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Hepatitis B virus (HBV) infection is a major cause of chronic liver disease that may progress to liver cirrhosis and hepatocellular carcinoma. Host immune responses represent the key determinants of HBV clearance or persistence. Here, we investigated the role of the early activation marker, CD69 and effector cytokines, granzyme B (GrB) and IFN- in the exhaustion of innate-like TCR V7.2(+)CD4(+)T cells, in 15 individuals with chronic HBV (CHB) infection where six were HBV DNA(+) and nine were HBV DNA(-). The percentage of cytokine-producing T cells and MAIT cells were significantly perturbed in HBV patients relative to healthy controls (HCs). The intracellular expression of GrB and IFN- was significantly reduced in MAIT cells derived from HBV-infected patients as compared to HCs, and the levels correlated with the percentage and levels [mean fluorescence intensity (MFI)] of CD69 expression. The total expression of CD69 (iMFI) was lower in CHB patients as compared to HCs. The frequency of CD69(+) cells correlated with the levels of cytokine expression (MFI), particularly in CHB patients as compared to HCs. In summary, the polyfunctionality of peripheral T cells was significantly reduced among CHB patients, especially in the TCR V7.2(+)CD4(+)T cells, and the levels of cytokine expression correlated with functional cytokine levels.

Ort, förlag, år, upplaga, sidor
SAGE PUBLICATIONS LTD , 2017. Vol. 23, nr 5, s. 459-467
Nyckelord [en]
CD69; cytotoxic cells; HBV infection; immune exhaustion; innate-like T cells; MAIT cells
Nationell ämneskategori
Cell- och molekylärbiologi
Identifikatorer
URN: urn:nbn:se:liu:diva-139616DOI: 10.1177/1753425917714854ISI: 000405306000006PubMedID: 28606013OAI: oai:DiVA.org:liu-139616DiVA, id: diva2:1133742
Anmärkning

Funding Agencies|Universiti Malaya Research Grant (UMRG) [RP021A-13HTM, HIR E000063]

Tillgänglig från: 2017-08-16 Skapad: 2017-08-16 Senast uppdaterad: 2018-01-13

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Larsson, Marie
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Avdelningen för mikrobiologi och molekylär medicinMedicinska fakulteten
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Innate Immunity
Cell- och molekylärbiologi

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