Evidence map›Paper›PMID 28586386›Full record

ArticlePloS one2017

Differential Th17 response induced by the two clades of the pandemic ST258 Klebsiella pneumoniae clonal lineages producing KPC-type carbapenemase.

Ann Maria Clemente, Giuseppe Castronovo, Alberto Antonelli, Marco Maria D'Andrea, Michele Tanturli, Eloisa Perissi, Sara Paccosi, Astrid Parenti, Federico Cozzolino, Gian Maria Rossolini and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.5field-weighted citation impact, top 43% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Differential virulence potential of different clades of multidrug-resistantmedRxiv : the preprint server for health sciences · 2026
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  7. Reduced antigenicity of Omicron lowers host serologic response.bioRxiv : the preprint server for biology · 2022
    Article
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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

11 authors at 2 institutions in 1 country.

Ann Maria ClementeDepartment of Experimental and Clinical Medicine, University of Firenze, Firenze, Italy.
Giuseppe CastronovoDepartment of Experimental and Clinical Medicine, University of Firenze, Firenze, Italy.
Alberto AntonelliDepartment of Experimental and Clinical Medicine, University of Firenze, Firenze, Italy.
Marco Maria D'AndreaDepartment of Experimental and Clinical Medicine, University of Firenze, Firenze, Italy.
Michele TanturliDepartment of Experimental and Clinical Biomedical Sciences, University of Firenze, Firenze, Italy.
Eloisa PerissiDepartment of Experimental and Clinical Medicine, University of Firenze, Firenze, Italy.
Sara PaccosiDepartment of Health Science, University of Firenze, Firenze, Italy.
Astrid ParentiDepartment of Health Science, University of Firenze, Firenze, Italy.
Federico CozzolinoDepartment of Experimental and Clinical Biomedical Sciences, University of Firenze, Firenze, Italy.
Gian Maria RossoliniDepartment of Experimental and Clinical Medicine, University of Firenze, Firenze, Italy.
Maria Gabriella TorciaDepartment of Experimental and Clinical Medicine, University of Firenze, Firenze, Italy.ORCID http://orcid.org/0000-0003-4740-4646
University of Florence · ITUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The spread of KPC-type carbapenemases is mainly attributed to the global dissemination of Klebsiella pneumoniae (KP) strains belonging to the clonal group (CG) 258, including sequence type (ST) 258 and other related STs. Two distinct clades of CG258-KP have evolved, which differ mainly for the composition of their capsular polysaccharides, and recent studies indicate that clade 1 evolved from an ancestor of clade 2 by recombination of a genomic fragment carrying the capsular polysaccharide (cps) locus. In this paper, we investigated the ability of two ST258-KP strains, KKBO-1 and KK207-1, selected as representatives of ST258-KP clade 2 and clade 1, respectively, to activate an adaptive immune response using ex vivo-stimulation of PBMC from normal donors as an experimental model. Our data showed that KKBO-1 (clade 2) induces a Th17 response more efficiently than KK207-1 (clade 1): the percentage of CD4+IL17+ cells and the production of IL-17A were significantly higher in cultures with KKBO-1 compared to cultures with KK207-1. While no differences in the rate of bacterial internalization or in the bacteria-induced expression of CD86 and HLA-DR by monocytes and myeloid dendritic cells were revealed, we found that the two strains significantly differ in inducing the production of cytokines involved in the adaptive immune response, as IL-1β, IL-23 and TNF-α, by antigen-presenting cells, with KKBO-1 being a more efficient inducer than KK207-1. The immune responses elicited by KK207-1 were comparable to those elicited by CIP 52.145, a highly virulent K. pneumoniae reference strain known to escape immune-inflammatory responses. Altogether, present results suggest that CG258-KP of the two clades are capable of inducing a different response of adaptive immunity in the human host.

Indexed as

Adaptive ImmunityAntigen-Presenting CellsB7-2 AntigenBacterial Proteinsbeta-LactamasesCD4-Positive T-LymphocytesDendritic CellsGenome, BacterialHLA-DR AntigensHost-Pathogen InteractionsHumansInterleukin-17Klebsiella InfectionsKlebsiella pneumoniaePhylogenyTh17 CellsB7-2 AntigenBacterial Proteinsbeta-LactamasescarbapenemaseHLA-DR AntigensInterleukin-17Tumor Necrosis Factor-alpha

Identifiers

PMID28586386
PMCPMC5460819
OpenAlexW2623547472

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.