Clinical Articles Open Access
Copyright ©The Author(s) 1996. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Sep 15, 1996; 2(3): 173-175
Published online Sep 15, 1996. doi: 10.3748/wjg.v2.i3.173
Assessment of natural and interleukin-2-induced production of interferon-gamma in patients with liver diseases
Shi-Bao Chen, Xiao-Hui Miao, Ping Du, Qing-Xuan Wu
Shi-Bao Chen, Xiao-Hui Miao, Department of Gastroenterology, Changzheng Hospital, Second Military Medical University, Shanghai 200003, China
Ping Du, Qing-Xuan Wu, Department of Microbiology, Second Military Medical University, Shanghai 200433, China
Shi-Bao Chen, Professor of Internal Medicine, advisor of postgraduate for doctorate, having 84 papers published
Author contributions: All authors contributed equally to the work.
Supported by National Science Foundation of China. No.89138970378.
Correspondence to: Dr. Shi-Bao Chen, Professor, Department of Gastroenterology, Changzheng Hospital, Second Military Medical University, Shanghai 200003, China
Telephone: +86-21-63275997-361
Received: July 8, 1996
Revised: August 9, 1996
Accepted: August 24, 1996
Published online: September 15, 1996

Abstract

AIM: To determine whether the production of lower interferon gamma (IFNl) by lymphocytes in patients with liver diseases is due to defects of the lymphocytes themselves or to other cofactors, such as interleukin-2 (IL-2).

METHODS: Peripheral blood mononuclear cells (PBMCs) from patients with various liver diseases were cultured with or without phytohemagglutinin (PHA) and IL-2. The cells were harvested and counted, and the supernatants were tested for IFNl by a sensitive and quantitative ABC-enzyme-linked immunosorbent assay (ELISA).

RESULTS: IFNl was not found in serum samples from patients or normal individuals. However, IFNl was detectable in supernatants of non-induced and induced PBMCs by ABC-ELISA. In non-induced PBMCs (group 1), the content of IFNl in supernatants from control, chronic active hepatitis (CAH), chronic persistent hepatitis (CPH), and hepatocellular carcinoma (HCC) was 8.72/L, 5.03/L, 6.02/L, and 4.91/L, respectively. The production of IFNl in liver disease was significantly decreased compared to control. In PBMCs stimulated with PHA (group 2), the content of IFNl was 22.71/L, 17.12/L, 14.54/L, and 17.63/L, respectively. In PBMCs induced by IL-2 (group 3), the amount of IFNl in supernatant from control (60.67/L) was much larger than those from CAH (21.70/L), CPH (24.00/L), and HCC (19.15/L) (p < 0.01). When comparing the amount of IFNl in group 3 with that in group 1, we found that IFNl production was enhanced by nearly 4-folds in liver diseases and by over 7-fold in control. In contrast, the number of PBMCs, whether from liver diseases or from control, was increased by only approximately 3-fold.

CONCLUSION: The decreased production of IFNl in liver diseases, including HCC, is mainly due to endogenous defects of lymphocytes but may also involve a decrease in stimulating cofactors, such as IL-2.

Key Words: Liver disease, Interleukin-2, Interferon type II



INTRODUCTION

Abnormal immune function is an important mechanism of hepatitis B virus (HBV) infection-related liver diseases and hepatocellular carcinoma (HCC)[1]. It was previously shown that disruption of cellular-mediated immune function, including defects in the production of lymphokines, is involved in HBV infection and HCC[2,3]. Interferon-gamma (IFNγ), one of the most important cytokines with various activities, plays a key role in immunoregulation. It has been suggested that IFNγ production by lymphocytes is correlated with the cause, development, and prognosis of chronic liver diseases[4]. However, it is not clear whether the decrease of IFNγ production is caused by defective secretion of IFNγ producing lymphocytes, by decreased levels of inducing cofactors, such as interleukin-2 (IL-2), or both. In the present study, we measured IL-2-induced IFNγ production in peripheral blood mononuclear cells (PBMCs) in order to evaluate the relationship between IFNγ production and liver diseases.

MATERIALS AND METHODS
Subjects

Twenty-one patients with chronic HBV infection (19 males and two females, 15-63 years old), including 12 cases of chronic persistent hepatitis (CPH) (three cases with cirrhosis) and nine cases of chronic active hepatitis (CAH), and nine patients with HCC (eight males and one female, 15-57 years old) were studied. The diagnoses were confirmed by clinical characteristics, laboratory analyses, and imaging examinations. Ten healthy blood donors served as controls.

Preparation of PBMCs

Five milliliters of venous blood were collected and heparinized. PBMCs were isolated from whole heparinized blood by centrifugation over Ficoll, washed three times with Roswell Park Memorial Institute (RPMI)-1640 medium (Gibco, Carlsbad, CA, United States), and then suspended at 2 × 106 cells/mL in RPMI-1640 medium containing 10% fetal calf serum. The viability of cells was higher than 95% by the trypan blue exclusive test.

Induction of IFNγ from PBMCs

Each PBMC sample was placed in a 96-well plate (2 × 105 cells/100 μL per well) in three groups. For each group, double wells were designed. In group 1, 100 μL of medium was added and cultured without any inducers. In group 2, 100 μL of 1:100 diluted phytohemagglutinin (PHA) (type M. Sigma, St Louis, MO, United States) was added. In group 3, 100 μL of IL-2 (gift from the Department of Microbiology, SMMC) with the activity of 2 × 103 U/mL was added. The cells were incubated at 37 °C in 5% CO2 for 72 h, and the culture supernatants were removed and tested for IFNγ. The cells were counted under a light microscope.

Detection of IFNγ

IFNγ in supernatants was detected by a quantitative ABC-enzyme linked immune sorbent assay (ELISA), as we previously described[5].

Statistical analysis

Data were analyzed by Student’s t test and F test.

RESULTS
IFNγ in serum samples

IFNγ was not detected in the sera of 21 patients with chronic HBV infection, the nine patients with HCC, or any of the controls.

IFNγ production by PBMCs in normal individuals

The amount of IFNγ produced in non-induced supernatants was 8.72 ± 0.65 μg/L (n = 10). Stimulation with PHA and IL-2 with increasing time durations and dosages significantly enhanced the production of IFNγ (p < 0.01). The relationships between course and effectiveness and between dosage and effectiveness are indicated in Figure 1 and Figure 2.

Figure 1
Figure 1 Interferon gamma (IFNγ) production by normal peripheral blood mononuclear cells (PBMCs) over time.
Figure 2
Figure 2 IFNγ production by normal PBMCs induced by various dosages of interleukin (IL)-2.
Comparison of IFNγ production in various liver diseases

IFNγ production in either PHA-induced or non-induced PBMCs in liver diseases was significantly lower than that in normal individuals (P < 0.01). Although the production of IFNγ was the lowest in HCC patients, there was no significant difference in IFNγ production among various liver diseases (P > 0.05). The level of IFNγ was increased in the supernatants of IL-2 induced PBMCs from patients with CPH, CAH, and HCC, respectively, compared with non-induced PBMCs (Figure 3).

Figure 3
Figure 3 IFNγ production by PBMCs from patients with liver diseases and from normal individuals.
The number of IL-2 induced PBMCs

The number of IL-2 induced PBMCs was increased approximately 3 times compared to non-induced PBMCs in liver diseases and in control. When comparing the increase of IFNγ production (by 6.9 times in control, 4.3 times in CAH, 4.0 times in CPH and 3.9 times in HCC) with the increase in the number of PBMCs, we found that there was a difference between them.

DISCUSSION

Recently, the importance of cytokines in immunoregulation has been recognized, and the correlation between cytokines and body disorders is continuing to be elucidated[6]. The dysfunction of cellular immunity is an important mechanism of HBV infection-related chronic liver diseases and is associated with persistent HBV infection[7].

Some new therapies for HBV infection, such as the application of IFNs and lymphokine activated killer (LAK) cells, are partially effective for the clearance of HBV[8]. More recently, cytokine gene transfer therapy for HBV infection and HCC has also been reported[9]. All these therapies are based on findings that the production of cytokines is decreased in hepatitis B and that the replacement of cytokines is an effective way to maintain balance of the immune system. In this study, we found that IFNγ production by non-induced and lymphoblastized PBMCs from patients with various chronic liver diseases and HCC was significantly lower than that in normal individuals, with the lowest in patients with cirrhosis. These findings suggest that IFNγ producing cells, i.e., T helper and natural killer (NK) cells, may be defective in the production of IFNγ. Among the factors that stimulate the production of IFNγ, IL-2 is the most important[10]. In this study, when PBMCs were cultured with IL-2, the secretion of IFNγ was enhanced 3.9 (in HCC) to 6.8 (in control) fold, whereas the number of PBMCs was increased by only 3 times, suggesting that the enhancement of IFNγ production was related not only to the increase in PBMC number but also to the enhancement in the IFNγ producing ability of PBMCs. It was reported that LAK cell therapy was shortly effective for suppression of HBV duplication. These authors suggested that the increase in cytokine production of LAK cells was involved in the anti-HBV mechanism[7]. Our results are consistent with these findings.

However, the inducing effects of IL-2 on IFNγ production are not the same in patients with liver diseases and normal controls. In patients with liver diseases, the amount of IFNγ produced by IL-2 induction in PBMCs was nearly 7 times greater than that in non-induced PBMCs; whereas in normal controls, the former is about 4 times greater than the latter. We conclude that the decreased production of IFNγ in patients with liver diseases is mainly due to endogenous defects of lymphocytes but may also be due to a decrease in some stimulating cofactors.

Notably, we failed to detect IFNγ directly from the sera of patients or normal individuals by a sensitive and quantitative ABC-ELISA established in our laboratory. Some other authors reported similar results by CPE. It may be concluded that the level of IFNγ secreted in serum is too small to be detected by the present methods. Moreover, the amount of IFNγ in serum may be influenced by many factors, such as the half-life of IFNγ, liver and renal function, and the time of collecting blood. Therefore, we recommend for future studies on cytokines, including IFNγ, the preparation of lymphocytes or PBMCs rather than serum.

Footnotes

Original title: China National Journal of New Gastroenterology (1995-1997) renamed World Journal of Gastroenterology (1998-).

S- Editor: Tao T L- Editor: Filipodia E- Editor: Li RF

References
1.  Peters M, Davis GL, Dooley TS. The interferon system in acute and chronic viral hepatitis. Progress in liver disease. Vol. New York: Grune & Stratton 1986; 453-467.  [PubMed]  [DOI]  [Cited in This Article: ]
2.  Kato Y, Nakagawa H, Kobayashi K, Hattori N, Hatano K. Interferon production by peripheral lymphocytes in HBsAg-positive liver diseases. Hepatology. 1982;2:789-790.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 58]  [Cited by in F6Publishing: 58]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
3.  Saibara T, Maeda T, Miyazaki M, Onishi S, Yamamoto Y. Assessment of lymphokine-activated killer activity and gamma-interferon production in patients with small hepatocellular carcinomas. Hepatology. 1993;17:781-787.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 6]  [Article Influence: 0.2]  [Reference Citation Analysis (0)]
4.  Fuji A, Kakumu S, Ohtani Y, Murase K, Hirofuji H, Tahara H. Interferon-gamma production by peripheral blood mononuclear cells of patients with chronic liver disease. Hepatology. 1987;7:577-581.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 37]  [Cited by in F6Publishing: 37]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
5.  Miao XH, Pan W, Wu QX, Du P, Chen SB, Qi ZT. An ABC-ELISA to detect human natural and recombinant interferon-gamma. Zhonghua Weishengwuxue He Mianyixue Zazhi. 1994;14:58-61.  [PubMed]  [DOI]  [Cited in This Article: ]
6.  Peters M, Vierling J, Gershwin ME, Milich D, Chisari FV, Hoofnagle JH. Immunology and the liver. Hepatology. 1991;13:977-994.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 92]  [Cited by in F6Publishing: 84]  [Article Influence: 2.9]  [Reference Citation Analysis (0)]
7.  Dienstag JL Immunologic mechanisms in chronic viral hepatitis. In: Vyas GN, Dienstag JL, Hoofnagle JH, eds. Viral hepatitis and liver disease. New York, Grune & Stratton 1984; 135-166.  [PubMed]  [DOI]  [Cited in This Article: ]
8.  Bissett J, Eisenberg M, Gregory P, Robinson WS, Merigan TC. Recombinant fibroblast interferon and immune interferon for treating chronic hepatitis B virus infection: patients’ tolerance and the effect on viral markers. J Infect Dis. 1988;157:1076-1080.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 17]  [Cited by in F6Publishing: 17]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]
9.  Ledley FD. Hepatic gene therapy: present and future. Hepatology. 1993;18:1263-1273.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 39]  [Cited by in F6Publishing: 39]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
10.  Farrar WL, Johnson HM, Farrar JJ. Regulation of the production of immune interferon and cytotoxic T lymphocytes by interleukin 2. J Immunol. 1981;126:1120-1125.  [PubMed]  [DOI]  [Cited in This Article: ]