<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(5)</volume><submitter>Wu ZQ</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The seroconversion of the hepatitis B antigen is the ideal outcome for long-acting interferon-pegylated interferon-α (Peg-IFN-α) treatment among patients with chronic hepatitis B (CHB). B-cell response plays an important role in the process of hepatitis B antigen clearance, but the specific mechanism by which B-cell improve hepatitis B virus (HBV) is still unclear.&lt;h4>Methods&lt;/h4>A total of 103 CHB patients participated in this study. The patients received 24 weeks of Peg-IFN-α treatment. Flow cytometry was used to detect B-cell surface markers' cluster of differentiation cluster of differentiation CD19, CD24, and CD27 in the peripheral blood mononuclear cells (PBMCs) of CHB patients before and after 24 weeks of Peg-IFN-α treatment.&lt;h4>Results&lt;/h4>After 24 weeks of Peg-IFN-α treatment, the content of memory B cells (CD19&lt;sup>+&lt;/sup>CD27&lt;sup>+&lt;/sup>) and effector B cells (CD19&lt;sup>+&lt;/sup>CD38&lt;sup>+&lt;/sup>) increased significantly. Further analysis showed that the clearance of the hepatitis B antigen was correlated with the change value, ΔT, of plasma cells before and after treatment. The B-cell subsets (CD19&lt;sup>+&lt;/sup>CD24&lt;sup>+&lt;/sup>; CD19&lt;sup>+&lt;/sup>CD40&lt;sup>+&lt;/sup>; CD19&lt;sup>+&lt;/sup>CD40&lt;sup>+&lt;/sup>; CD19&lt;sup>+&lt;/sup>CD80&lt;sup>+&lt;/sup>), was also tested and the results showed that CD19&lt;sup>+&lt;/sup>CD24&lt;sup>+&lt;/sup> and CD19&lt;sup>+&lt;/sup>CD80&lt;sup>+&lt;/sup> content also increased significantly after treatment.&lt;h4>Conclusions&lt;/h4>After Peg-IFN-α treatment, the B-cell subsets of CHB patients are remodeled. Thus, Peg-IFN-α treatment appears to play an important role in the remodeling of B cell subsets and the clearance of HBV antigens. The results of this study provide a theoretical basis and guidance for the clinical treatment of CHB.</pubmed_abstract><journal>Annals of translational medicine</journal><pagination>414</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8033293</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The relationship between the clearance of HBsAg and the remodeling of B cell subsets in CHB patients treated with Peg-IFN-α.</pubmed_title><pmcid>PMC8033293</pmcid><pubmed_authors>Tan L</pubmed_authors><pubmed_authors>Xie DY</pubmed_authors><pubmed_authors>Wu ZQ</pubmed_authors><pubmed_authors>Gan WQ</pubmed_authors><pubmed_authors>Mo ZS</pubmed_authors><pubmed_authors>Chen DB</pubmed_authors><pubmed_authors>Wang PP</pubmed_authors><pubmed_authors>Gao ZL</pubmed_authors><pubmed_authors>Zhao QY</pubmed_authors></additional><is_claimable>false</is_claimable><name>The relationship between the clearance of HBsAg and the remodeling of B cell subsets in CHB patients treated with Peg-IFN-α.</name><description>&lt;h4>Background&lt;/h4>The seroconversion of the hepatitis B antigen is the ideal outcome for long-acting interferon-pegylated interferon-α (Peg-IFN-α) treatment among patients with chronic hepatitis B (CHB). B-cell response plays an important role in the process of hepatitis B antigen clearance, but the specific mechanism by which B-cell improve hepatitis B virus (HBV) is still unclear.&lt;h4>Methods&lt;/h4>A total of 103 CHB patients participated in this study. The patients received 24 weeks of Peg-IFN-α treatment. Flow cytometry was used to detect B-cell surface markers' cluster of differentiation cluster of differentiation CD19, CD24, and CD27 in the peripheral blood mononuclear cells (PBMCs) of CHB patients before and after 24 weeks of Peg-IFN-α treatment.&lt;h4>Results&lt;/h4>After 24 weeks of Peg-IFN-α treatment, the content of memory B cells (CD19&lt;sup>+&lt;/sup>CD27&lt;sup>+&lt;/sup>) and effector B cells (CD19&lt;sup>+&lt;/sup>CD38&lt;sup>+&lt;/sup>) increased significantly. Further analysis showed that the clearance of the hepatitis B antigen was correlated with the change value, ΔT, of plasma cells before and after treatment. The B-cell subsets (CD19&lt;sup>+&lt;/sup>CD24&lt;sup>+&lt;/sup>; CD19&lt;sup>+&lt;/sup>CD40&lt;sup>+&lt;/sup>; CD19&lt;sup>+&lt;/sup>CD40&lt;sup>+&lt;/sup>; CD19&lt;sup>+&lt;/sup>CD80&lt;sup>+&lt;/sup>), was also tested and the results showed that CD19&lt;sup>+&lt;/sup>CD24&lt;sup>+&lt;/sup> and CD19&lt;sup>+&lt;/sup>CD80&lt;sup>+&lt;/sup> content also increased significantly after treatment.&lt;h4>Conclusions&lt;/h4>After Peg-IFN-α treatment, the B-cell subsets of CHB patients are remodeled. Thus, Peg-IFN-α treatment appears to play an important role in the remodeling of B cell subsets and the clearance of HBV antigens. The results of this study provide a theoretical basis and guidance for the clinical treatment of CHB.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-04T21:24:50.868Z</modification><creation>2025-04-04T21:24:50.868Z</creation></dates><accession>S-EPMC8033293</accession><cross_references><pubmed>33842635</pubmed><doi>10.21037/atm-21-409</doi></cross_references></HashMap>