Comparative Analysis of Liver Injury-Associated Cytokines in Acute Hepatitis A and B

So Youn Shin; Sook-Hyang Jeong; Pil Soo Sung; Jino Lee; Hyung Joon Kim; Hyun Woong Lee; Eui-Cheol Shin

doi:10.3349/ymj.2016.57.3.652

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Shin, Jeong, Sung, Lee, Kim, Lee, and Shin: Comparative Analysis of Liver Injury-Associated Cytokines in Acute Hepatitis A and B

Original Article

Gastroenterology & Hepatology

Yonsei Medical Journal 2016; 57(3): 652-657.

Published online: 15 March 2016

DOI: https://doi.org/10.3349/ymj.2016.57.3.652

Comparative Analysis of Liver Injury-Associated Cytokines in Acute Hepatitis A and B

So Youn Shin^1,^2,^*, Sook-Hyang Jeong^3,^*, Pil Soo Sung¹, Jino Lee¹, Hyung Joon Kim⁴, Hyun Woong Lee⁴, Eui-Cheol Shin¹

¹Laboratory of Immunology and Infectious Diseases, Graduate School of Medical Science and Engineering, KAIST, Daejeon, Korea.

²Department of Infectious Diseases, International St. Mary's Hospital, Catholic Kwandong University College of Medicine, Incheon, Korea.

³Department of Internal Medicine, Seoul National University Bundang Hospital, College of Medicine, Seoul National University, Seongnam, Korea.

⁴Department of Internal Medicine, Chung-Ang University Hospital, Seoul, Korea.

Corresponding author: Dr. Eui-Cheol Shin, Laboratory of Immunology and Infectious Diseases, Graduate School of Medical Science and Engineering, KAIST, 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Korea. Tel: 82-42-350-4236, Fax: 82-42-350-4240, ecshin@kaist.ac.kr

Equal contributor:

*So Youn Shin and Sook-Hyang Jeong contributed equally to this work.

Received 6 August 2015 Revised 31 August 2015 Accepted 31 August 2015

(open-access):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Purpose

Acute hepatitis A (AHA) and acute hepatitis B (AHB) are caused by an acute infection of the hepatitis A virus and the hepatitis B virus, respectively. In both AHA and AHB, liver injury is known to be mediated by immune cells and cytokines. In this study, we measured serum levels of various cytokines and T-cell cytotoxic proteins in patients with AHA or AHB to identify liver injury-associated cytokines.

Materials and Methods

Forty-six patients with AHA, 16 patients with AHB, and 14 healthy adults were enrolled in the study. Serum levels of 17 cytokines and T-cell cytotoxic proteins were measured by enzyme-linked immunosorbent assays or cytometric bead arrays and analyzed for correlation with serum alanine aminotransferase (ALT) levels.

Results

Interleukin (IL)-18, IL-8, CXCL9, and CXCL10 were significantly elevated in both AHA and AHB. IL-6, IL-22, granzyme B, and soluble Fas ligand (sFasL) were elevated in AHA but not in AHB. In both AHA and AHB, the serum level of CXCL10 significantly correlated with the peak ALT level. Additionally, the serum level of granzyme B in AHA and the serum level of sFasL in AHB correlated with the peak ALT level.

Conclusion

We identified cytokines and T-cell cytotoxic proteins associated with liver injury in AHA and AHB. These findings deepen the existing understanding of immunological mechanisms responsible for liver injury in acute viral hepatitis.

Keywords: Hepatitis A virus, hepatitis B virus, liver injury, cytokines, chemokines

INTRODUCTION

Hepatitis A virus (HAV) is a non-enveloped, single-stranded RNA virus of the Picornaviridae family.1 HAV infection is often asymptomatic in children. However, HAV infection in adults tends to result in acute hepatitis, called acute hepatitis A (AHA), one of the most common forms of acute viral hepatitis.2 3 4 In adult patients with AHA, severe liver injury and jaundice frequently develop and last for several weeks. However, AHA resolves spontaneously in most cases and does not progress to chronic viral hepatitis.5

Hepatitis B virus (HBV) is a partly double-stranded DNA virus that belongs to the Hepadnaviridae family.6 HBV infection is the most common form of chronic viral infection in the world, with more than 350 million people chronically infected.7 In endemic areas, chronic HBV infection is often established by vertical transmission.8 In adults, acute HBV infection causes acute hepatitis B (AHB), which is accompanied by liver injury and jaundice.8 9 Although AHB resolves spontaneously in most adult patients, some cases (1–5%) progress to chronic persistent infection.8 9

In both AHA and AHB, liver injury is known to be caused by T cells, not by the virus, because both HAV and HBV are non-cytopathic viruses.9 10 11 Immune-mediated tissue injury, so-called immunopathology, is mediated by diverse mechanisms in different viral infections.12 The inflammatory process is mediated by cytokines, including interleukin (IL)-1β, IL-6, and tumor necrosis factor-α (TNF-α), and it is suppressed by IL-10.12 Additionally, helper 1 T (Th1) cells and helper 17 T (Th17) cells contribute to tissue injury by secreting cytokines; e.g., Th1 cells secrete interferon (IFN)-γ and TNF-α, and Th17 cells secrete IL-17 and IL-21.13 Moreover, cytotoxic T cells and natural killer (NK) cells directly lyse host cells through perforin/granzyme, and Fas ligand-mediated mechanisms.14 Chemokines are also involved in immune-mediated tissue injury by recruiting immune cells to the site of a viral infection.15 16 However, in AHA and AHB, the exact mechanisms of immune-mediated liver injury remain to be elucidated.

In this study, we measured serum levels of 17 cytokines and T-cell cytotoxic proteins in patients with AHA and AHB in the acute phase to understand immunological mechanisms of liver injury in acute viral hepatitis, and identified cytokines or T-cell cytotoxic proteins associated with severe liver injury in AHA and AHB. The present study provides insight regarding which effector function of T cells contributes to liver injury in AHA and AHB.

MATERIALS AND METHODS

Study participants

Forty-six patients with AHA, 16 patients with AHB, and 14 healthy adults were recruited from hospitals in the Seoul metropolitan area (Seoul National University Bundang Hospital, Chung-Ang University Hospital, Bundang CHA Hospital, Seongnam Central Hospital, and Daejin Medical Center). AHA and AHB were diagnosed based on positive detection with anti-HAV IgM, and HBsAg and anti-HBc IgM, respectively, typical disease symptoms, and elevated serum alanine aminotransferase (ALT) levels. Peak ALT level and peak total bilirubin level were determined for each patient during the course of acute hepatitis. We obtained informed consent from participating subjects and study approval from the Institutional Review Boards. At the time of hospital admission, blood was drawn from patients, and serum samples were frozen for later analysis.

Analysis of serum cytokines

Eleven cytokines: IL-1β, IL-6, IL-10, IL-12p70, IL-18, IL-21, IL-22, IL-28, IL-29, IFN-γ, and TNF-α; and four chemokines: IL-8, CCL2 (monocyte chemoattractant protein-1), CXCL9 (monokine induced by IFN-γ), and CXCL10 (IFN-γ-inducible protein-10) were measured in this study. We also analyzed the serum levels of T-cell cytotoxic proteins, including granzyme B and soluble Fas ligand (sFasL). The serum levels of these proteins were measured with either enzyme-linked immunosorbent assay (ELISA) kits (IL-18, Abcam, Cambridge, UK; IL-22, R&D Systems, Minneapolis, MN, USA; and IL-28 and IL-29, RayBiotech Inc., Norcross, GA, USA) or cytometric bead array flex kits (BD Biosciences, San Jose, CA, USA).

Statistical analysis

Discrete variables were compared using the χ² method, and independent t tests were used for continuous variables. Pearson or Spearman correlation analysis was used to determine simple correlations between continuous variables. All statistical analyses were performed with Statistical Product and Service Solutions 13.0. (SPSS Inc., Chicago, IL, USA).

RESULTS

General characteristics of enrolled patients

Table 1 shows the demographic and laboratory characteristics of the study population. The median age of the AHA patients, AHB patients, and healthy controls were 33.6, 35.8, and 32.1 years, respectively. The average of peak ALT levels (IU/L) was 4450 in AHA patients and 1406 in AHB patients. The average of peak total bilirubin levels (mg/dL) was 5.1 in AHA patients and 9.6 in AHB patients.

Serum levels of cytokines, chemokines, and T-cell cytotoxic proteins in AHA and AHB

Among the serum proteins analyzed, several were significantly elevated in serum samples from patients with AHA or AHB, compared to serum samples from healthy subjects. IL-18, IL-8, CXCL9, and CXCL10 were significantly elevated in both AHA and AHB, whereas IL-6, IL-22, granzyme B, and sFasL were significantly elevated in AHA, but not in AHB (Fig. 1).

Correlation between the serum levels of CXCR3 chemokines and liver injury

Next, we analyzed which chemokines were associated with the degree of liver injury, assessing liver injury in terms of serum ALT levels. CXCL10 and CXCL9 are CXCR3 chemokines and known to be elevated frequently in systemic viral infections.17 Fig. 2 shows that CXCL10 levels were significantly correlated with peak ALT levels in both AHA and AHB, whereas the serum CXCL9 levels were correlated with peak ALT levels in AHA, but tended to correlate with peak ALT levels in AHB (Fig. 2B).

Correlation between the serum levels of cytokines or T-cell cytotoxic proteins and liver injury

Next, we investigated which cytokines or T-cell cytotoxic proteins were associated with peak ALT levels. In AHA, serum granzyme B, but not serum sFasL, was significantly correlated with peak ALT levels (Fig. 3A). Conversely, in AHB, serum sFasL but not serum granzyme B was significantly correlated with peak ALT levels (Fig. 3B). In addition, the serum IL-18 levels significantly correlated with peak total bilirubin levels in AHA (Fig. 3C) but not in AHB (Fig. 3D). We also analyzed IL-22, a known hepatoprotective cytokine.18 19 20 However, the serum IL-22 levels did not correlate with peak ALT levels in either AHA or AHB (data not shown).

DISCUSSION

In the present study, we found that the serum levels of IL-18, IL-8, CXCL9, and CXCL10 were elevated in AHA and AHB. In addition, the serum levels of IL-6, IL-22, granzyme B and sFasL were increased in AHA but not in AHB, indicating that AHA is accompanied by more vigorous immune responses compared to AHB. The levels of CXCR3 ligands, CXCL10 and CXCL9 correlated with peak ALT levels in AHA and AHB. Moreover, serum granzyme B levels correlated with peak ALT levels in AHA, and serum sFasL levels correlated with peak ALT levels in AHB. These findings together suggest that effector functions of T cells are elevated and contribute to liver injury in AHA and AHB.

CXCR3 and its ligand chemokines regulate the migration of Th1 cells and effector CD8⁺ T cells into infection sites during various human and murine acute viral infections, such as influenza,21 dengue,22 and West Nile virus infection.23 In viral hepatitis, CXCR3 chemokines have been studied, particularly in hepatitis C virus (HCV) infection. CXCR3 chemokines are detected in the peripheral blood 2–8 weeks after HCV infection.24 25 26 The expression level of CXCR3 chemokines in the liver or the peripheral blood correlated well with the severity of hepatic inflammation in patients with chronic HCV infection.27 28 29 30 In ch-ronic HBV infection, it was demonstrated that serum CXCL10 and CXCL9 levels are associated with the acute flare-up of liver injury.31 Consistent with these reports, our data from the sera of AHA and AHB patients demonstrated that CXCR3 chemokines are increased during AHA and AHB, and that their levels correlate with liver damage, thus implying that they might play an important role in liver injury.

Notably, our present data also showed that serum granzyme B levels correlated with peak ALT levels in AHA (Fig. 3A), and that serum sFasL levels correlated with peak ALT levels in AHB (Fig. 3B). The correlation between serum sFasL and serum ALT levels was previously reported in self-limited AHB and fulminant hepatitis B.32 CD8⁺ cytotoxic T cells and NK cells can contribute to liver injury by target cell-killing activity. When these cells are triggered, they exert cytotoxic activity through two different mechanisms: degranulation of perforin and granzymes, and upregulation of FasL on their cell surface.33 The current findings indicate that a distinct cytotoxic mechanism might contribute to hepatocyte destruction in AHA and AHB.

In the present study, we examined serum levels of cytokines and T-cell cytotoxic proteins to evaluate immune responses during AHA and AHB. However, we did not examine immune cells such as T cells and NK cells, therefore, we do not know yet which subsets of immune cells produce the cytokines and cytotoxic proteins that are increased in the sera of AHA and AHB patients. Future studies should investigate the expression levels of cytokines and cytotoxic proteins in T cells and NK cells obtained from patients with AHA or AHB.

Recently, the levels of multiple serum proteins were systematically analyzed in blood drawn from patients with AHA, AHB, and acute hepatitis C.34 However, that study did not consider the levels of serum proteins relative to the degree of liver injury. In the present study, we compared the associations between liver injury and cytokines, chemokines, and T-cell cytotoxic proteins in AHA and AHB. Our present findings led us to propose that distinct immunological mechanisms of liver injury might operate in AHA and AHB. The exact mechanisms of liver injury require further investigation at the cellular and molecular levels in acute viral hepatitis.

Figures and Tables

Fig. 1

Serum levels of cytokines, chemokines, and T-cell cytotoxic proteins in AHA and AHB. The data represent the serum proteins that were elevated in patients with AHA or AHB compared to healthy controls. Horizontal lines indicate mean values; n=46 for AHA, n=16 for AHB, and n=14 for healthy controls. p values are presented as *p<0.01 or ^†p<0.001, based on the unpaired Student's t-test. IL, interleukin; AHA, acute hepatitis A; AHB, acute hepatitis B.

Fig. 2

Correlation between the serum levels of CXCR3 chemokines and the degree of liver injury. Serum concentrations of CXCL10 (A) and CXCL9 (B) correlated to peak ALT levels in samples drawn from patients with AHA (left) or AHB (right). Correlation coefficients (r) are based on Pearson (AHA) or Spearman (AHB) analyses. p values <0.05 are considered statistically significant. AHA, acute hepatitis A; AHB, acute hepatitis B; ALT, alanine aminotransferase.

Fig. 3

Correlation between the serum levels of cytokines or T-cell cytotoxic proteins and the degree of liver injury. Serum concentrations of granzyme B (left), sFasL (center), or IL-18 (right) correlated to peak ALT levels (A and B) or peak total bilirubin levels (C and D) in samples drawn from patients with AHA (A and C) or AHB (B and D). Correlation coefficients (r) are based on Pearson (AHA) or Spearman (AHB) analyses. p values<0.05 are considered statistically significant. n.s., non-significant; sFasL, soluble Fas ligand; IL, interleukin; AHA, acute hepatitis A; AHB, acute hepatitis B; ALT, alanine aminotransferase.

Table 1

Demographic and Laboratory Characteristics of the Study Population

	Patients with AHA (n=46)	Patients with AHB (n=16)	Healthy controls (n=14)
Gender (male; number and %)	26 (56.5)	13 (81.3)	12 (85.7)
Age (yrs; median and range)	33.6 (22-49)	35.8 (19-67)	32.1 (24-44)
Peak ALT (IU/L; median and IQR)	2828 (1351-4031)	2042 (1489-2919)	n.d.
Peak AST (IU/L; median and IQR)	3255 (757-5325)	1010 (711-1502)	n.d.
Peak total bilirubin (mg/dL; median and IQR)	4.9 (3.2-7.0)	7.2 (3.9-12.4)	n.d.

IQR, interquartile range; n.d., not determined; AHA, acute hepatitis A; AHB, acute hepatitis B; ALT, alanine aminotransferase; AST, aspartate aminotransferase.

ACKNOWLEDGEMENTS

This study was supported by a grant from the Korea Health Technology R&D Project of the Ministry of Health & Welfare, Republic of Korea (HI13C1263) and by a grant from the SNUBH Research Fund (03-2011-010).

Notes

The authors have no financial conflicts of interest.

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