CEACAM1 Is Associated With the Suppression of Natural Killer Cell Function in Patients With Chronic Hepatitis C

Natural killer cells (NK cells) play an essential role in the immunological mechanism underlying chronic hepatitis C (CHC). Impairment of NK cell function facilitates persistent infection with hepatitis C virus (HCV) and hepatocellular carcinogenesis. However, the mechanism by which NK cell activity...

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Main Authors: Takahiro Suda, Tomohide Tatsumi, Akira Nishio, Tadashi Kegasawa, Teppei Yoshioka, Ryoko Yamada, Kunimaro Furuta, Takahiro Kodama, Minoru Shigekawa, Hayato Hikita, Ryotaro Sakamori, Takasuke Fukuhara, Yoshiharu Matsuura, Tetsuo Takehara
Format: Article
Language:English
Published: Wolters Kluwer Health/LWW 2018-10-01
Series:Hepatology Communications
Online Access:https://doi.org/10.1002/hep4.1240
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author Takahiro Suda
Tomohide Tatsumi
Akira Nishio
Tadashi Kegasawa
Teppei Yoshioka
Ryoko Yamada
Kunimaro Furuta
Takahiro Kodama
Minoru Shigekawa
Hayato Hikita
Ryotaro Sakamori
Takasuke Fukuhara
Yoshiharu Matsuura
Tetsuo Takehara
author_facet Takahiro Suda
Tomohide Tatsumi
Akira Nishio
Tadashi Kegasawa
Teppei Yoshioka
Ryoko Yamada
Kunimaro Furuta
Takahiro Kodama
Minoru Shigekawa
Hayato Hikita
Ryotaro Sakamori
Takasuke Fukuhara
Yoshiharu Matsuura
Tetsuo Takehara
author_sort Takahiro Suda
collection DOAJ
description Natural killer cells (NK cells) play an essential role in the immunological mechanism underlying chronic hepatitis C (CHC). Impairment of NK cell function facilitates persistent infection with hepatitis C virus (HCV) and hepatocellular carcinogenesis. However, the mechanism by which NK cell activity is suppressed in CHC is not completely understood. In this study, we focused on carcinoembryonic antigen–related cell‐adhesion molecule 1 (CEACAM1). CEACAM1 is thought to suppress NK cell function. We examined the effect of CEACAM1 on NK cell function in CHC. We investigated the function of CEACAM1 in vitro using Huh7.5.1 cells and the HCV‐Japanese fulminant hepatitis (JFH)‐1 strain. We analyzed serum CEACAM1 level, NK cell function, and CEACAM1 messenger RNA (mRNA) level in human liver samples. Levels of CEACAM1 on the cell surface, CEACAM1 mRNA levels, and soluble CEACAM1 levels in supernatants were significantly higher in Huh7.5.1 cells infected with JFH‐1 (Huh7.5.1/JFH‐1 cells) than in Huh7.5.1 cells. Significantly higher NK cell cytotoxicity was observed toward K562 cells after coculture with CEACAM1 knockout Huh7.5.1/JFH‐1 cells than after coculture with Huh7.5.1/JFH‐1 cells. CEACAM1 expression was induced by the HCV E2 glycoprotein in HCV infection. Significantly higher serum CEACAM1 levels were detected in patients with CHC compared with healthy subjects and patients who achieved sustained virological responses. The expression of CD107a on NK cells from patients with CHC was negatively correlated with serum CEACAM1 levels. Significantly higher levels of CEACAM1 mRNA were detected in HCV‐infected livers compared with uninfected livers. Conclusion: CEACAM1 expression was induced in hepatocytes following HCV infection and decreased NK cell cytotoxicity. These results demonstrate a possible role for CEACAM1 in the pathogenesis of CHC and hepatocellular carcinoma progression.
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spelling doaj.art-65d403062b09423f9034ffca652a172f2023-02-02T12:32:29ZengWolters Kluwer Health/LWWHepatology Communications2471-254X2018-10-012101247125810.1002/hep4.1240CEACAM1 Is Associated With the Suppression of Natural Killer Cell Function in Patients With Chronic Hepatitis CTakahiro Suda0Tomohide Tatsumi1Akira Nishio2Tadashi Kegasawa3Teppei Yoshioka4Ryoko Yamada5Kunimaro Furuta6Takahiro Kodama7Minoru Shigekawa8Hayato Hikita9Ryotaro Sakamori10Takasuke Fukuhara11Yoshiharu Matsuura12Tetsuo Takehara13Department of Gastroenterology and Hepatology Osaka University Graduate School of Medicine Suita JapanDepartment of Gastroenterology and Hepatology Osaka University Graduate School of Medicine Suita JapanDepartment of Gastroenterology and Hepatology Osaka University Graduate School of Medicine Suita JapanDepartment of Gastroenterology and Hepatology Osaka University Graduate School of Medicine Suita JapanDepartment of Gastroenterology and Hepatology Osaka University Graduate School of Medicine Suita JapanDepartment of Gastroenterology and Hepatology Osaka University Graduate School of Medicine Suita JapanDepartment of Gastroenterology and Hepatology Osaka University Graduate School of Medicine Suita JapanDepartment of Gastroenterology and Hepatology Osaka University Graduate School of Medicine Suita JapanDepartment of Gastroenterology and Hepatology Osaka University Graduate School of Medicine Suita JapanDepartment of Gastroenterology and Hepatology Osaka University Graduate School of Medicine Suita JapanDepartment of Gastroenterology and Hepatology Osaka University Graduate School of Medicine Suita JapanDepartment of Molecular Virology Research Institute for Microbial Diseases, Osaka University Suita JapanDepartment of Molecular Virology Research Institute for Microbial Diseases, Osaka University Suita JapanDepartment of Gastroenterology and Hepatology Osaka University Graduate School of Medicine Suita JapanNatural killer cells (NK cells) play an essential role in the immunological mechanism underlying chronic hepatitis C (CHC). Impairment of NK cell function facilitates persistent infection with hepatitis C virus (HCV) and hepatocellular carcinogenesis. However, the mechanism by which NK cell activity is suppressed in CHC is not completely understood. In this study, we focused on carcinoembryonic antigen–related cell‐adhesion molecule 1 (CEACAM1). CEACAM1 is thought to suppress NK cell function. We examined the effect of CEACAM1 on NK cell function in CHC. We investigated the function of CEACAM1 in vitro using Huh7.5.1 cells and the HCV‐Japanese fulminant hepatitis (JFH)‐1 strain. We analyzed serum CEACAM1 level, NK cell function, and CEACAM1 messenger RNA (mRNA) level in human liver samples. Levels of CEACAM1 on the cell surface, CEACAM1 mRNA levels, and soluble CEACAM1 levels in supernatants were significantly higher in Huh7.5.1 cells infected with JFH‐1 (Huh7.5.1/JFH‐1 cells) than in Huh7.5.1 cells. Significantly higher NK cell cytotoxicity was observed toward K562 cells after coculture with CEACAM1 knockout Huh7.5.1/JFH‐1 cells than after coculture with Huh7.5.1/JFH‐1 cells. CEACAM1 expression was induced by the HCV E2 glycoprotein in HCV infection. Significantly higher serum CEACAM1 levels were detected in patients with CHC compared with healthy subjects and patients who achieved sustained virological responses. The expression of CD107a on NK cells from patients with CHC was negatively correlated with serum CEACAM1 levels. Significantly higher levels of CEACAM1 mRNA were detected in HCV‐infected livers compared with uninfected livers. Conclusion: CEACAM1 expression was induced in hepatocytes following HCV infection and decreased NK cell cytotoxicity. These results demonstrate a possible role for CEACAM1 in the pathogenesis of CHC and hepatocellular carcinoma progression.https://doi.org/10.1002/hep4.1240
spellingShingle Takahiro Suda
Tomohide Tatsumi
Akira Nishio
Tadashi Kegasawa
Teppei Yoshioka
Ryoko Yamada
Kunimaro Furuta
Takahiro Kodama
Minoru Shigekawa
Hayato Hikita
Ryotaro Sakamori
Takasuke Fukuhara
Yoshiharu Matsuura
Tetsuo Takehara
CEACAM1 Is Associated With the Suppression of Natural Killer Cell Function in Patients With Chronic Hepatitis C
Hepatology Communications
title CEACAM1 Is Associated With the Suppression of Natural Killer Cell Function in Patients With Chronic Hepatitis C
title_full CEACAM1 Is Associated With the Suppression of Natural Killer Cell Function in Patients With Chronic Hepatitis C
title_fullStr CEACAM1 Is Associated With the Suppression of Natural Killer Cell Function in Patients With Chronic Hepatitis C
title_full_unstemmed CEACAM1 Is Associated With the Suppression of Natural Killer Cell Function in Patients With Chronic Hepatitis C
title_short CEACAM1 Is Associated With the Suppression of Natural Killer Cell Function in Patients With Chronic Hepatitis C
title_sort ceacam1 is associated with the suppression of natural killer cell function in patients with chronic hepatitis c
url https://doi.org/10.1002/hep4.1240
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