Plasma interferon-gamma-inducible-protein 10 level as a predictive factor of spontaneous hepatitis B surface antigen seroclearance in chronic hepatitis B patients

被引:2
作者
Kan, Karin [1 ,2 ]
Wong, Danny Ka-Ho [1 ,2 ]
Hui, Rex Wan-Hin [1 ]
Seto, Wai Kay [1 ,2 ]
Yuen, Man-Fung [1 ,2 ]
Mak, Lung-Yi [1 ,2 ]
机构
[1] Univ Hong Kong, Sch Clin Med, Dept Med, Pokfulam Rd 102, Hong Kong, Peoples R China
[2] Univ Hong Kong, State Key Lab Liver Res, Hong Kong, Peoples R China
关键词
cytokines; hepatitis B surface antigen; hepatitis B virus; IP-10; seroclearance; HBSAG SEROCLEARANCE; MESSENGER-RNA; VIRAL CONTROL; LIVER-DAMAGE; SERUM-LEVELS; EXPRESSION; THERAPY; IP-10; SEROCONVERSION; INTERLEUKIN-2;
D O I
10.1111/jgh.16371
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aim: Spontaneous seroclearance of hepatitis B surface antigen (HBsAg) is a rare event that occurs in patients that are chronically infected with the hepatitis B virus. As the functional cure and ultimate treatment endpoint of chronic hepatitis B (CHB), HBsAg seroclearance is an important milestone in the natural history of CHB and serves great clinical value. This study aims to identify host and viral factors associated with HBsAg seroclearance.Methods: This is a retrospective study carried out in the Queen Mary Hospital, Hong Kong. By analyzing the plasma retrieved from the serum archive (collected during 2011-2021) of 100 CHB patients attending the hospital's liver clinic, the longitudinal cytokine profiles between the HBsAg-losers and the control groups were compared.Results; Data revealed that plasma levels of IP-10 were significantly lower at 3-5 years prior to HBsAg seroclearance compared with patients who remained HBsAg positive (P < 0.05). Receiver operating characteristic curve analysis reveals that plasma IP-10 levels at multiple time points before HBsAg seroclearance return area under receivor-operating characteristic curve (AUC) greater than 0.7. Plasma IP-10 levels at 42.39 pg/mL produced an AUC = 0.723 with 74.0% sensitivity and 75.5% specificity to predict subsequent HBsAg seroclearance in the next 3-5 years. Low plasma IP-10 identified 91.4% patients with quantitative HBsAg < 100 IU/mL who would subsequently develop HBsAg seroclearance, compared with 37% with higher plasma IP-10 levels (P < 0.001).Conclusion: sLow plasma levels of IP-10 are associated with subsequent HBsAg seroclearance, suggesting potential clinical utilities of measurement of IP-10 in predicting HBsAg seroclearance, especially among patients with low HBsAg.
引用
收藏
页码:202 / 209
页数:8
相关论文
共 41 条
[1]   Does increased body mass index with hepatic steatosis contribute to seroclearance of hepatitis B virus (HBV) surface antigen in chronic HBV infection? [J].
Chu, C-M ;
Lin, D-Y ;
Liaw, Y-F .
INTERNATIONAL JOURNAL OF OBESITY, 2007, 31 (05) :871-875
[2]   Clinical and Virological Characteristics Post HBsAg Seroclearance in Hepatitis B Virus Carriers With Hepatic Steatosis Versus Those Without [J].
Chu, Chia-Ming ;
Lin, Deng-Yn ;
Liaw, Yun-Fan .
DIGESTIVE DISEASES AND SCIENCES, 2013, 58 (01) :275-281
[3]   Prerequisites for cytokine measurements in clinical trials with multiplex immunoassays [J].
de Jager, Wilco ;
Bourcier, Katarzyna ;
Rijkers, Ger T. ;
Prakken, Berent J. ;
Seyfert-Margolis, Vicki .
BMC IMMUNOLOGY, 2009, 10 :52
[4]   EASL 2017 Clinical Practice Guidelines on the management of hepatitis B virus infection [J].
Lampertico P. ;
Agarwal K. ;
Berg T. ;
Buti M. ;
Janssen H.L.A. ;
Papatheodoridis G. ;
Zoulim F. ;
Tacke F. .
JOURNAL OF HEPATOLOGY, 2017, 67 (02) :370-398
[5]  
Geneva-Popova M, 1999, Folia Med (Plovdiv), V41, P78
[6]  
Ghany MG, 2023, HEPATOLOGY, V78, P1654, DOI [10.1097/HEP.0000000000000431, 10.1016/j.jhep.2023.06.002]
[7]  
Gong LL, 2015, INT J CLIN EXP PATHO, V8, P8367
[8]   INTERLEUKIN-2 DOWN-REGULATES HEPATITIS-B VIRUS GENE-EXPRESSION IN TRANSGENIC MICE BY A POSTTRANSCRIPTIONAL MECHANISM [J].
GUILHOT, S ;
GUIDOTTI, LG ;
CHISARI, FV .
JOURNAL OF VIROLOGY, 1993, 67 (12) :7444-7449
[9]   Hepatitis B surface antigen (HBsAg) decrease and serum interferon-inducible protein-10 levels as predictive markers for HBsAg loss during treatment with nucleoside/nucleotide analogues [J].
Jaroszewicz, Jerzy ;
Ho, Huy ;
Markova, Antoaneta ;
Deterding, Katja ;
Wursthorn, Karsten ;
Schulz, Sandra ;
Bock, Claus-Thomas ;
Tillmann, Hans L. ;
Manns, Michael P. ;
Wedemeyer, Heiner ;
Cornberg, Markus .
ANTIVIRAL THERAPY, 2011, 16 (06) :915-924
[10]   Blocking chemokine responsive to γ-2/interferon (IFN)-γ inducible protein and monokine induced by IFN-γ activity in vivo reduces the pathogenetic but not the antiviral potential of hepatitis B virus-specific cytotoxic T lymphocytes [J].
Kakimi, K ;
Lane, TE ;
Wieland, S ;
Asensio, VC ;
Campbell, IL ;
Chisari, FV ;
Guidotti, LG .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (12) :1755-1766