Evidence map›Paper›PMID 41501704›Full record

ArticleBMC infectious diseases2026

Association of PD-1

Jiangyu Liu, Ling Qin, Zichen Zhang, Daqiong Zhou, Dacheng Sheng, Minyu Duan, Zhenhuan Cao

Abstract read
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Jiangyu LiuBeijing Youan Hospital, Capital Medical University, No.8, Xitou Alley, Outer, You'an Gate, Fengtai, Beijing, China.
Ling QinBeijing Youan Hospital, Capital Medical University, No.8, Xitou Alley, Outer, You'an Gate, Fengtai, Beijing, China.
Zichen ZhangBeijing Youan Hospital, Capital Medical University, No.8, Xitou Alley, Outer, You'an Gate, Fengtai, Beijing, China.
Daqiong ZhouBeijing Youan Hospital, Capital Medical University, No.8, Xitou Alley, Outer, You'an Gate, Fengtai, Beijing, China.
Dacheng ShengBeijing Youan Hospital, Capital Medical University, No.8, Xitou Alley, Outer, You'an Gate, Fengtai, Beijing, China.
Minyu DuanBeijing Youan Hospital, Capital Medical University, No.8, Xitou Alley, Outer, You'an Gate, Fengtai, Beijing, China.
Zhenhuan CaoBeijing Youan Hospital, Capital Medical University, No.8, Xitou Alley, Outer, You'an Gate, Fengtai, Beijing, China. caozhenhuanyu@mail.ccmu.edu.cn.ORCID http://orcid.org/0000-0003-4204-1049

Funding

Capital's Funds for Health Improvement and Research [2024-1-2182]Laboratory for Clinical Medicine, Capital Medical University [SYLH2023-04]
6 · The paper itself

Abstract

backgroundPrevious studies by our group and others have demonstrated that pegylated interferon (PEG-IFN) therapy results in a relatively high rate of clinical cure in inactive hepatitis B surface antigen carriers (IHCs). Emerging evidence suggests that B lymphocytes play a pivotal role in HBsAg clearance. This study aimed to evaluate the efficacy of PEG-IFN in IHCs, investigate dynamic changes in global (non-HBV-specific) B-cell subset frequencies and their association with HBsAg clearance, and characterize the immunological profiles of B cells in CHB patients who achieved a functional cure.

methodsA total of 458 inactive IHCs who were enrolled at Beijing You’an Hospital, Capital Medical University, between January 2008 and February 2023 were included in this study. All participants received once-weekly subcutaneous injections of PEG-IFNα-2b, and clinical outcomes were retrospectively analyzed in the entire cohort. B-cell phenotyping was performed in a subset of 36 patients (21 with HBsAg clearance and 15 without) to assess the frequencies of PD-1⁺ and IgG⁺ B-cell subsets, including total B cells, plasmablasts, naïve B cells, immature B cells, and memory B cells. These assessments were conducted at baseline and at weeks 12 and 24 of treatment.

resultsClinical cure rates were 15.98% at week 24 and 28.27% at week 48 of PEG-IFN therapy. At week 24, the frequency of PD-1⁺ total B cells was significantly lower in the C group than in the NC group (0.63% vs. 1.61%, P = 0.037). The proportion of IgG⁺ plasmablasts was significantly higher in the C group compared to the NC group (10% vs. 5.5%, P = 0.016).

conclusionIHCs who achieved HBsAg clearance under PEG-IFN therapy had lower PD-1⁺ total B-cell frequencies and relatively higher proportions of IgG⁺ plasmablasts than those without clearance. These findings show limited observational differences in PD-1⁺ B-cell and IgG⁺ plasmablast frequencies between groups, which may be associated with clinical cure, but the biological implications remain uncertain and warrant confirmation in larger mechanistic studies.

Indexed as

Antiviral AgentsB-LymphocytesHepatitis B, ChronicImmunoglobulin GInterferon-alphaPlasma CellsPolyethylene GlycolsProgrammed Cell Death 1 ReceptorAdultB-Lymphocyte SubsetsFemaleHepatitis B Surface AntigensHumansInterferon alpha-2MaleMiddle AgedAntiviral AgentsHepatitis B Surface AntigensImmunoglobulin GInterferon-alphaInterferon alpha-2PDCD1 protein, humanpeginterferon alfa-2bPolyethylene GlycolsProgrammed Cell Death 1 ReceptorRecombinant ProteinsB cellsHBsAg clearanceInactive HBsAg carriers (IHCs)Peginterferon (PEG-IFN)Programmed cell death protein 1 (PD-1)

Identifiers

PMID41501704
PMCPMC12882490

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.