Low Level of Serum Immunoglobulin G Is Beneficial to Clinical Cure Obtained With Pegylated Interferon Therapy in Inactive Surface Antigen Carriers.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2022
Historique:
received: 28 01 2022
accepted: 24 03 2022
entrez: 9 5 2022
pubmed: 10 5 2022
medline: 11 5 2022
Statut: epublish

Résumé

Our recent study showed a high rate of HBsAg clearance in inactive HBsAg carriers (IHCs) treated with pegylated IFN (PEG-IFN). To better understand the immune-mediated component of HBsAg clearance, this study investigated the role of serum immunoglobulin G (IgG) and its subclasses in predicting HBsAg clearance in IHCs with PEG-IFN therapy. In this study, IHCs received PEG-IFN for 96 weeks. Subjects who achieved clearance of HBsAg were considered responders (R group), and those in whom HBsAg was not cleared were considered non-responders (NR group). The HBsAg, ALT, and serum lgG subtypes (lgG1, IgG2, IgG3, lgG4) were tested at baseline, and at 12 and 24 weeks of treatment. To evaluate the factors in predicting HBsAg clearance, univariate and multivariate logistic regression analyses were performed. The receiver operator characteristic curves and the area under the receiver operator characteristic curve (AUROC) were used to evaluate prognostic values. Our results showed that 39 cases obtained HBsAg clearance (group R), while 21 cases did not (group NR). There was no significant difference in age, ALT, and AST levels between the two groups. The serum levels of IgG1, lgG2, lgG3 and lgG4 at baseline, and at 12 and 24 weeks were significantly lower in IHC with HBsAg clearance than in the NR group. Univariate logistic regression analysis showed that serum IgG1, IgG2, IgG3, and IgG4 levels at baseline, and at 12, and 24 weeks were all strong predictors of HBsAg clearance. In all indicators, lgG2 had the highest AUROC at baseline and lgG3 the highest AUROC at week 12. A multifactor logistic analysis was performed with y=33.933-0.001*BaselinelgG1-0.002*BaselinelgG2. The area under the curve was 0.941 with 100% sensitivity and 76.19% specificity. Together, our findings suggest that serum IgG has a higher predictive value compared to the convention predictors of HBsAg and ALT for HBsAg clearance and thus may be a better clinical predictor of HBsAg clearance in IHCs.

Identifiants

pubmed: 35529845
doi: 10.3389/fimmu.2022.864354
pmc: PMC9073012
doi:

Substances chimiques

Antigens, Surface 0
Antiviral Agents 0
Hepatitis B Surface Antigens 0
Immunoglobulin G 0
Interferon-alpha 0
Polyethylene Glycols 3WJQ0SDW1A

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

864354

Informations de copyright

Copyright © 2022 Li, Lin, Liu, Qin, Zheng, Liu, Wei, Liang, Liu, Zhang, Chen and Cao.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Hong Li (H)

The Third Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.

Xiao Lin (X)

The First Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.

Lili Liu (L)

The Third Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.

Ling Qin (L)

Biomedical Information Center, Beijing Youan Hospital, Capital Medical University, Beijing, China.

Yanhong Zheng (Y)

The First Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.

Xiaohui Liu (X)

The Third Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.

Xinhuan Wei (X)

The Third Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.

Shan Liang (S)

The Third Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.

Yali Liu (Y)

The Third Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.

Jing Zhang (J)

The Third Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.

Xinyue Chen (X)

The First Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.

Zhenhuan Cao (Z)

The Third Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.

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Classifications MeSH