Evidence map›Paper›PMID 41089688›Full record

ReviewFrontiers in immunology2025

Developmental trajectory of long-lived plasma cells.

Takuya Koike, Wataru Ise

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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

2 authors.

Takuya KoikeRegulation of Host Defense Team, Division of Microbiology and Immunology, Center for Infectious Disease Education and Research, The University of Osaka, Osaka, Japan.
Wataru IseRegulation of Host Defense Team, Division of Microbiology and Immunology, Center for Infectious Disease Education and Research, The University of Osaka, Osaka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long-lived plasma cells (LLPCs), which continuously secrete antibodies, play a central role in humoral immunity and form the foundation of effective vaccine strategies. The anatomical segregation between the tissues where plasma cells are generated and where they are maintained suggests that both cell-intrinsic and extrinsic factors contribute to their longevity; however, the underlying cellular and molecular mechanisms remain largely unclear. In this review, we summarize recent advances in elucidating the regulation of plasma cell survival at both induction and effector sites. We particularly highlight potential LLPC precursors among newly generated plasma cells in secondary lymphoid tissues, and their subsequent maturation and differentiation into bona fide LLPCs within the bone marrow.

Indexed as

Cell DifferentiationPlasma CellsAnimalsCell SurvivalHumansImmunity, Humoralantibodybone marrowLLPCnichevaccine

Identifiers

PMID41089688
PMCPMC12515943

What OpenQuestion holds

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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 OpenQuestion graph.