Evidence map›Paper›PMID 29540686›Full record

ArticleNature communications2018

A non-conserved amino acid variant regulates differential signalling between human and mouse CD28.

Nicla Porciello, Paola Grazioli, Antonio F Campese, Martina Kunkl, Silvana Caristi, Marta Mastrogiovanni, Michela Muscolini, Francesca Spadaro, Cédric Favre, Jacques A Nunès and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

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  17. The Evolving Role of CD8International journal of molecular sciences · 2019
    Review
  18. 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

14 authors at 5 institutions in 4 countries.

Nicla PorcielloDepartment of Biology and Biotechnology Charles Darwin, Laboratory Affiliated at Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Sapienza University, 00185, Rome, Italy.
Paola GrazioliDepartment of Experimental Medicine, Sapienza University, 00161, Rome, Italy.
Antonio F CampeseDepartment of Molecular Medicine, Laboratory Affiliated at Istituto Pasteur-Fondazione Cenci Bolognetti, Sapienza University, 00161, Rome, Italy.
Martina KunklDepartment of Biology and Biotechnology Charles Darwin, Laboratory Affiliated at Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Sapienza University, 00185, Rome, Italy.
Silvana CaristiDepartment of Biology and Biotechnology Charles Darwin, Laboratory Affiliated at Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Sapienza University, 00185, Rome, Italy.
Marta MastrogiovanniDepartment of Biology and Biotechnology Charles Darwin, Laboratory Affiliated at Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Sapienza University, 00185, Rome, Italy.
Michela MuscoliniIstituto Pasteur-Fondazione Cenci Bolognetti, 00161, Rome, Italy.
Francesca SpadaroConfocal Microscopy Unit NMR and Confocal Microscopy Area Core Facilities, Istituto Superiore di Sanità, 00161, Rome, Italy.
Cédric FavreCentre de Recherche en Cancérologie de Marseille, Immunity and Cancer Team, Institut Paoli Calmettes, Inserm U1068, CNRS, UMR7258, Aix-Marseille Université UM 105, 13284, Marseille, France.
Jacques A NunèsCentre de Recherche en Cancérologie de Marseille, Immunity and Cancer Team, Institut Paoli Calmettes, Inserm U1068, CNRS, UMR7258, Aix-Marseille Université UM 105, 13284, Marseille, France.ORCID http://orcid.org/0000-0003-4865-0400
Aldo BorrotoCentro de Biología Molecular Severo Ochoa, Spanish National Research Council-Autonomous University of Madrid (CSIC-UAM), 28049, Madrid, Spain.
Balbino AlarconCentro de Biología Molecular Severo Ochoa, Spanish National Research Council-Autonomous University of Madrid (CSIC-UAM), 28049, Madrid, Spain.
Isabella ScrepantiDepartment of Molecular Medicine, Laboratory Affiliated at Istituto Pasteur-Fondazione Cenci Bolognetti, Sapienza University, 00161, Rome, Italy.
Loretta TuostoDepartment of Biology and Biotechnology Charles Darwin, Laboratory Affiliated at Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Sapienza University, 00185, Rome, Italy. loretta.tuosto@uniroma1.it.
Istituto Pasteur · ITCentre National de la Recherche Scientifique · FRConsejo Superior de Investigaciones Científicas · ESIstituto Superiore di Sanità · ITSapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD28 superagonistic antibodies (CD28SAb) can preferentially activate and expand immunosuppressive regulatory T cells (Treg) in mice. However, pre-clinical trials assessing CD28SAbs for the therapy of autoimmune diseases reveal severe systemic inflammatory response syndrome in humans, thereby implying the existence of distinct signalling abilities between human and mouse CD28. Here, we show that a single amino acid variant within the C-terminal proline-rich motif of human and mouse CD28 (P

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAutoimmune DiseasesCD28 AntigensHumansLymphocyte ActivationMiceNF-kappa BOncogene ProteinsProtein BindingSignal TransductionT-Lymphocytes, RegulatoryAdaptor Proteins, Signal TransducingCD28 AntigensNck proteinNF-kappa BOncogene Proteins

Identifiers

PMID29540686
PMCPMC5852078
OpenAlexW2789914923

What OpenQuestion holds

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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.