Evidence map›Paper›PMID 38453885›Full record

ReviewCell death discovery2024

B cell memory: from generation to reactivation: a multipronged defense wall against pathogens.

Madiha Zahra Syeda, Tu Hong, Chunming Huang, Wenhua Huang, Qingchun Mu

Open access · goldAbstract readReview
In one paragraph

Review in Cell death discovery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
16.1field-weighted citation impact, top 1% 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

55 citing papers in PubMed, 67 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  5. Review
  6. CNS1-dependent regulatory T cells shape recovery from acute lung injury.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Article
  7. Review
  8. Article
  9. Article
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  11. Review
  12. Article
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  14. Extending ImmunoSpotVaccines · 2026
    Article
  15. Review
  16. Article
  17. Article
  18. Observational
  19. Article
  20. Review
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

5 authors at 4 institutions in 1 country.

Madiha Zahra Syeda *The People's Hospital of Gaozhou, Guangdong Medical University, Maoming, 525200, China.
Tu Hong *The First Affiliated Hospital, Zhejiang University, School of Medicine, 310058, Hangzhou, China.
Chunming HuangThe People's Hospital of Gaozhou, Guangdong Medical University, Maoming, 525200, China. huangcm@gdmu.edu.cn.
Wenhua HuangSchool of Basic Medical Sciences, Southern Medical University, Guangzhou, 510515, China. huangwenhua2009@139.com.ORCID http://orcid.org/0000-0003-2382-9180
Qingchun MuThe People's Hospital of Gaozhou, Guangdong Medical University, Maoming, 525200, China. muq@hainmc.edu.cn.ORCID http://orcid.org/0000-0001-7578-5381
Gaozhou People's Hospital · CNFirst Affiliated Hospital Zhejiang University · CNGuangdong Medical College · CNSouthern Medical University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82360366Natural Science Foundation of Guangdong Province (Guangdong Natural Science Foundation) 2023A1515012969
6 · The paper itself

Abstract

Development of B cell memory is a conundrum that scientists are still exploring. Studies have been conducted in vitro and using advanced animal models to elucidate the mechanism underlying the generation of memory B cells (MBCs), the precise roles of MBCs against pathogens, and their protective functions against repeated infections throughout life. Lifelong immunity against invading diseases is mainly the result of overcoming a single infection. This protection is largely mediated by the two main components of B cell memory-MBCs and long-lived plasma cells (PCs). The chemical and cellular mechanisms that encourage fat selection for MBCs or long-lived PCs are an area of active research. Despite the fact that nearly all available vaccinations rely on the capacity to elicit B-cell memory, we have yet to develop successful vaccines that can induce broad-scale protective MBCs against some of the deadliest diseases, including malaria and AIDS. A deeper understanding of the specific cellular and molecular pathways that govern the generation, function, and reactivation of MBCs is critical for overcoming the challenges associated with vaccine development. Here, we reviewed literature on the development of MBCs and their reactivation, interaction with other cell types, strategies against invading pathogens, and function throughout life and discussed the recent advances regarding the key signals and transcription factors which regulate B cell memory and their relevance to the quest for vaccine development.

Identifiers

PMID38453885
PMCPMC10920759
OpenAlexW4392557319

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.