Evidence map›Paper›PMID 35098838›Full record

ArticleAnnals of medicine2022

Comparison of the deep immune profiling of B cell subsets between healthy adults and Sjögren's syndrome.

Ruiling Feng, Jing Zhao, Feng Sun, Miao Miao, Xiaolin Sun, Jing He, Zhanguo Li

Open access · goldAbstract read
In one paragraph

Article in Annals of medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 9% of its field
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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. [Single-cell RNA sequencing of B cells reveals molecular typing in Sjögren syndrome].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2025
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  15. Increased frequency of IgD-CD27Arthritis research & therapy · 2022
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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 at 1 institution in 1 country.

Ruiling FengDepartment of Rheumatology & Immunology, Peking University People's Hospital, Beijing, China.ORCID 0000-0003-1465-3259
Jing ZhaoDepartment of Rheumatology & Immunology, Peking University People's Hospital, Beijing, China.ORCID 0000-0001-5824-0777
Feng SunDepartment of Rheumatology & Immunology, Peking University People's Hospital, Beijing, China.
Miao MiaoDepartment of Rheumatology & Immunology, Peking University People's Hospital, Beijing, China.
Xiaolin SunDepartment of Rheumatology & Immunology, Peking University People's Hospital, Beijing, China.
Jing HeDepartment of Rheumatology & Immunology, Peking University People's Hospital, Beijing, China.ORCID 0000-0003-3904-8928
Zhanguo LiDepartment of Rheumatology & Immunology, Peking University People's Hospital, Beijing, China.ORCID 0000-0002-2590-6242
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesDetailed analysis targeting B cell subgroups was considered crucial in monitoring autoimmune diseases and treatment responses. Thus, precisely describing the phenotypes of B cell differentiation and their variation in primary Sjögren's syndrome (pSS) is particularly needed.

methodsTo characterize the proportions and absolute counts of B cell subsets, peripheral blood from 114 healthy adults of China (age range: 19-73 years) and 55 patients with pSS were performed by flow cytometry and CD19, CD20, CD24, CD27, CD38 and IgD were used as surface markers to identify B cell mature process. Age- and gender-stratified analyses were then carried out to improve the interpretation of B cell subsets.

resultsThe assessments from healthy adults showed that the proportion of naive B cells presented a significant increase with age. A reversal trend was noted that the percentage of B10 decreased markedly with age. In addition, analysis based on gender showed that the relative percentage and number of naive B cells were higher in females than in males whereas the proportions of switched memory B cells and B10 cells were decreased in female. Patients with pSS exhibited a significant expansion in naïve B cells and unswitched memory B cells, accompanied with decreased switched memory B cells and B10 cells, which were identified to be associated with autoantibody production.

conclusionsOur study presented a reliable analysis by flow cytometry to cover the principal B cell subtypes. These different stages of B lymphocytes may have implications for evaluating the activation of pSS and other autoimmune diseases and treatment efficacy.KEY MESSAGESB cell subsets play a pivotal role in the pathogenesis of primary Sjögren's syndrome (pSS) and other autoimmune diseases. A practical and accurate flow cytometry method to profile B cell phenotypes in peripheral blood of healthy adults is especially essential.Additionally, we presented reliable reference ranges for B cell subsets in regards to the local population. Age- and gender-related analyses are available to better understand their influence in immune status and treatment outcome.The distribution of B-cell subsets is found substantially altered in patients with pSS, bringing novel avenues for pSS research in the future.

Indexed as

Autoimmune DiseasesB-Lymphocyte SubsetsSjogren's SyndromeB-LymphocytesFemaleFlow CytometryHumansMaleB cell subsetshealthy adultsmulticolour flow cytometryreference rangesSjögren’s syndrome

Identifiers

PMID35098838
PMCPMC8812739
OpenAlexW4210492720

What OpenQuestion holds

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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.