Evidence map›Paper›PMID 38305771›Full record

ReviewThe Journal of cell biology2024

Endolysosomal vesicles at the center of B cell activation.

Saara Hämälistö, Felipe Del Valle Batalla, María Isabel Yuseff, Pieta K Mattila

Open access · hybridAbstract readReview
In one paragraph

Review in The Journal of cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. 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

4 authors at 2 institutions in 2 countries.

Saara Hämälistö *Institute of Biomedicine, and MediCity Research Laboratories, University of Turku, Turku, Finland.ORCID 0000-0001-5348-4422
Felipe Del Valle Batalla *Laboratory of Immune Cell Biology, Department of Cellular and Molecular Biology, Pontificia Universidad Católica de Chile, Santiago, Chile.ORCID 0000-0001-6113-9549
María Isabel YuseffLaboratory of Immune Cell Biology, Department of Cellular and Molecular Biology, Pontificia Universidad Católica de Chile, Santiago, Chile.ORCID 0000-0001-8172-3785
Pieta K MattilaInstitute of Biomedicine, and MediCity Research Laboratories, University of Turku, Turku, Finland.ORCID 0000-0003-2805-0686
Åbo Akademi University · FIPontificia Universidad Católica de Chile · CL

Funding

Finnish Cultural foundationsFondo Nacional de Desarrollo Científico y Tecnológico 1221128Research Council of Finland 339810Sigrid Jusélius
6 · The paper itself

Abstract

The endolysosomal system specializes in degrading cellular components and is crucial to maintaining homeostasis and adapting rapidly to metabolic and environmental cues. Cells of the immune system exploit this network to process antigens or promote cell death by secreting lysosome-related vesicles. In B lymphocytes, lysosomes are harnessed to facilitate the extraction of antigens and to promote their processing into peptides for presentation to T cells, critical steps to mount protective high-affinity antibody responses. Intriguingly, lysosomal vesicles are now considered important signaling units within cells and also display secretory functions by releasing their content to the extracellular space. In this review, we focus on how B cells use pathways involved in the intracellular trafficking, secretion, and function of endolysosomes to promote adaptive immune responses. A basic understanding of such mechanisms poses an interesting frontier for the development of therapeutic strategies in the context of cancer and autoimmune diseases.

Indexed as

Adaptive ImmunityB-LymphocytesEndosomesLysosomesAnimalsAntigen PresentationAntigensHumansLymphocyte ActivationAntigens

Identifiers

PMID38305771
PMCPMC10837082
OpenAlexW4391485768

What OpenQuestion 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 OpenQuestion graph.