Evidence map›Paper›PMID 42844382›Full record

ReviewNature reviews. Immunology2026

A guide to B cell metabolism.

Yavuz F Yazicioglu, Glenn R Bantug, Christoph Hess, Alexander J Clarke

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Immunology, 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

4 authors.

Yavuz F YaziciogluDepartment of Biomedicine, Immunobiology, University of Basel, Basel, Switzerland. yavuzfurkan.yazicioglu@unibas.ch.ORCID http://orcid.org/0000-0003-3731-9333
Glenn R Bantug *Department of Biomedicine, Immunobiology, University of Basel, Basel, Switzerland.ORCID http://orcid.org/0000-0003-2253-6028
Christoph Hess *Department of Biomedicine, Immunobiology, University of Basel, Basel, Switzerland.
Alexander J Clarke *Kennedy Institute of Rheumatology, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0003-2846-7860

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The metabolism of immune cells must adapt dynamically to support their diverse functions. B cells, which are the key cellular mediators of humoral immunity, undergo extensive metabolic changes throughout their development and function, starting from their commitment to the B cell lineage in the bone marrow. In the periphery, further rounds of metabolic adaptation in B cells are driven by temporally regulated changes in signalling cues, energetic demands and nutrient availability within specialized tissue niches. Although they have historically been less well studied than other immune cell types, emerging evidence shows that B cells deploy mechanistically distinct metabolic strategies that are tightly linked to their effector identity. Recognizing B cell metabolism as its own biological entity is, therefore, crucial to the study of humoral immune responses. In this Review, we examine the metabolic pathways that regulate B cell homeostasis, their integration with cell signalling networks, and their adaptation to the metabolic environment across spatial and temporal scales. We further discuss how aberrations in these pathways can contribute to B cell-driven malignancies, autoimmunity, inborn errors of immunity, and B cell-tropic infections. We position B cell metabolism as a rapidly expanding frontier within immunometabolism in both health and disease.

Identifiers

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.