Evidence map›Paper›PMID 31957253›Full record

ArticleCellular microbiology2020

Shigella impairs human T lymphocyte responsiveness by hijacking actin cytoskeleton dynamics and T cell receptor vesicular trafficking.

Fatoumata Samassa, Mariana L Ferrari, Julien Husson, Anastassia Mikhailova, Ziv Porat, Florence Sidaner, Katja Brunner, Teck-Hui Teo, Elisabetta Frigimelica, Jean-Yves Tinevez and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Multifunctional antibody responses from a primateScience translational medicine · 2026
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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

13 authors at 5 institutions in 2 countries.

Fatoumata SamassaMolecular Microbial Pathogenesis Unit, Institut Pasteur, INSERM U1202, Paris, France.
Mariana L FerrariMolecular Microbial Pathogenesis Unit, Institut Pasteur, INSERM U1202, Paris, France.
Julien HussonLaboratoire d'Hydrodynamique (LadHyX), Ecole polytechnique, CNRS, Institut Polytechnique de Paris, Palaiseau, France.
Anastassia MikhailovaStructural Virology Unit, Institut Pasteur, Paris, France.
Ziv PoratFlow Cytometry Unit, Life Sciences Core Facility, Weizmann Institute of Sciences, Rehovot, Israel.
Florence SidanerProteigene, Saint Marcel, France.
Katja BrunnerMolecular Microbial Pathogenesis Unit, Institut Pasteur, INSERM U1202, Paris, France.
Teck-Hui TeoMolecular Microbial Pathogenesis Unit, Institut Pasteur, INSERM U1202, Paris, France.
Elisabetta FrigimelicaMolecular Microbial Pathogenesis Unit, Institut Pasteur, INSERM U1202, Paris, France.
Jean-Yves TinevezImage Analysis Hub, Institut Pasteur, Paris, France.
Philippe J SansonettiMolecular Microbial Pathogenesis Unit, Institut Pasteur, INSERM U1202, Paris, France.
Maria-Isabel ThoulouzeStructural Virology Unit, Institut Pasteur, Paris, France.
Armelle PhaliponMolecular Microbial Pathogenesis Unit, Institut Pasteur, INSERM U1202, Paris, France.ORCID 0000-0002-5769-1274
Inserm · FRInstitut Pasteur · FRCentre National de la Recherche Scientifique · FRSurgiMedia (France) · FRWeizmann Institute of Science · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Strategies employed by pathogenic enteric bacteria, such as Shigella, to subvert the host adaptive immunity are not well defined. Impairment of T lymphocyte chemotaxis by blockage of polarised edge formation has been reported upon Shigella infection. However, the functional impact of Shigella on T lymphocytes remains to be determined. Here, we show that Shigella modulates CD4+ T cell F-actin dynamics and increases cell cortical stiffness. The scanning ability of T lymphocytes when encountering antigen-presenting cells (APC) is subsequently impaired resulting in decreased cell-cell contacts (or conjugates) between the two cell types, as compared with non-infected T cells. In addition, the few conjugates established between the invaded T cells and APCs display no polarised delivery and accumulation of the T cell receptor to the contact zone characterising canonical immunological synapses. This is most likely due to the targeting of intracellular vesicular trafficking by the bacterial type III secretion system (T3SS) effectors IpaJ and VirA. The collective impact of these cellular reshapings by Shigella eventually results in T cell activation dampening. Altogether, these results highlight the combined action of T3SS effectors leading to T cell defects upon Shigella infection.

Indexed as

Adaptive ImmunityActin CytoskeletonActinsCell LineDysentery, BacillaryGolgi ApparatusHumansImmunological SynapsesProtein TransportReceptors, Antigen, T-CellShigellaT-LymphocytesType III Secretion SystemsActinsReceptors, Antigen, T-CellType III Secretion Systemsactincell polarisationGolgiimmunological synapseRab proteinsShigellaT3SS effectorsT cell activationTCRvesicular trafficking

Identifiers

PMID31957253
PMCPMC7187243
OpenAlexW3001272795

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.