Association of NKG2A with treatment for chronic hepatitis C virus infection

Harrison, R.J., Ettorre, A., Little, A-M. and Khakoo, S.I. (2010) Association of NKG2A with treatment for chronic hepatitis C virus infection Clinical and Experimental Immunology, 161, (2), pp. 306-314. (doi:10.1111/j.1365-2249.2010.04169.x). (PMID:20550548).


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Natural killer (NK) cells are critical to the immune response to viral infections. Their functions are controlled by receptors for major histocompatibility complex (MHC) class I, including NKG2A and killer-cell immunoglobulin-like receptors (KIR). In order to evaluate the role of MHC class I receptors in the immune response to hepatitis C virus infection we have studied patients with chronic HCV infection by multi-parameter flow cytometry directly ex vivo. This has permitted evaluation of combinatorial expression of activating and inhibitory receptors on single NK cells. Individuals with chronic HCV infection had fewer CD56(dim) NK cells than healthy controls (4.9 +/- 3.4% versus 9.0 +/- 5.9%, P < 0.05). Expression levels of the inhibitory receptor NKG2A was up-regulated on NK cells from individuals with chronic hepatitis C virus (HCV) (NKG2A mean fluorescence intensity 5692 +/- 2032 versus 4525 +/- 1646, P < 0.05). Twelve individuals were treated with pegylated interferon and ribavirin. This resulted in a down-regulation of NKG2A expression on CD56(dim) NK cells. Individuals with a sustained virological response (SVR) had greater numbers of NKG2A-positive, KIR-negative NK cells than those without SVR (27.6 +/- 9.6% NK cells versus 17.6 +/- 5.7, P < 0.02). Our data show that NKG2A expression is dysregulated in chronic HCV infection and that NKG2A-positive NK cells are associated with a beneficial response to pegylated interferon and ribavirin therapy.

Item Type: Article
Digital Object Identifier (DOI): doi:10.1111/j.1365-2249.2010.04169.x
ISSNs: 0009-9104 (print)
Keywords: hepatitis c, interferon-alpha, killer cell immunoglobulin-like receptors, natural killer cells, NKG2A

Organisations: Clinical & Experimental Sciences
ePrint ID: 336179
Date :
Date Event
August 2010Published
Date Deposited: 16 Mar 2012 13:54
Last Modified: 17 Apr 2017 17:24
Further Information:Google Scholar

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