Cirrhosis Hampers Early and Rapid Normalization of Natural Killer Cell Phenotype and Function in Hepatitis C Patients Undergoing Interferon-Free Therapy

被引:6
作者
Perpinan, Elena [1 ,2 ]
Perez-Del-Pulgar, Sofia [1 ,2 ]
Londono, Maria-Carlota [1 ,2 ]
Marino, Zoe [1 ,2 ]
Bartres, Concepcion [1 ,2 ]
Gonzalez, Patricia [1 ,2 ]
Garcia-Lopez, Mireia [1 ,2 ]
Pose, Elisa [1 ,2 ]
Lens, Sabela [1 ,2 ]
Maini, Mala K. [3 ]
Forns, Xavier [1 ,2 ]
Koutsoudakis, George [1 ,2 ]
机构
[1] Univ Barcelona, IDIBAPS, Hosp Clin, Liver Unit, Barcelona, Spain
[2] Ctr Invest Biomed Red Enfermedades Hepat & Digest, Barcelona, Spain
[3] UCL, Div Infect & Immun, London, England
基金
英国惠康基金;
关键词
hepatitis C virus; natural killer cells; direct-acting antivirals; immune restoration; cirrhosis; NK CELLS; STELLATE CELLS; IFN-GAMMA; LIVER; EXPRESSION; SUBSET; CYTOTOXICITY; MODULATION; RECEPTORS; HISTORY;
D O I
10.3389/fimmu.2020.00129
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Chronic hepatitis C virus (HCV) infection impairs natural killer (NK) cell phenotype and function. Whether restoration of NK cells occurs after successful interferon (IFN)-free therapies remains a controversial issue. Aim: To analyze how HCV-related liver cirrhosis impacts changes in NK cells prior and post-IFN-free therapies. Methods: NK cell analysis by multicolor flow cytometry was performed in HCV-infected patients with (n = 17) and without (n = 14) cirrhosis at baseline, week 4 during therapy, and weeks 12 and 48 after the end of therapy (FU12 and FU48, respectively). Non-HCV cirrhotic patients (n = 12) and healthy individuals (n = 12) served as controls. Results: At baseline, HCV cirrhotic patients presented an altered distribution of NK subsets (CD56(dim) and CD56(bright)) with higher expression of NKp46, HLA-DR, NKp30, KIR2DL2/L3, NKG2A, and CD85j receptors compared to healthy controls. All frequencies normalized by FU48, except for CD85j(+) cells. Likewise, substantial alterations were detected in NK cell function assessed by (i) signal transducer and activator of transcription 1 (STAT1) and phosphorylated levels of STAT1 and STAT4, (ii) degranulation (CD107a), (iii) cytotoxicity [tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)], and (iv) cytokine production [IFN-gamma and tumor necrosis factor-alpha (TNF-alpha)]. Of note, NK cell function at FU48 remained partially impaired. In contrast, non-cirrhotics showed normal baseline frequencies of HLA-DR-, NKG2A-, and CD85j-expressing NK cells. Importantly, altered baseline frequencies of NK cell subsets and NKp46(+) CD56(dim) cells, as well as NK cell function, were rapidly and completely restored. Conclusions: NK cell phenotype alterations persist after HCV eradication in cirrhotic patients, while their function is only partially restored, compromising immune restoration and immunosurveillance.
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页数:15
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