Evidence map›Paper›PMID 30092791›Full record

ArticleMolecular neurodegeneration2018

Counteracting roles of MHCI and CD8

Giovanni Nardo, Maria Chiara Trolese, Mattia Verderio, Alessandro Mariani, Massimiliano de Paola, Nilo Riva, Giorgia Dina, Nicolò Panini, Eugenio Erba, Angelo Quattrini and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular neurodegeneration, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 7% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

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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 1 institution in 1 country.

Giovanni NardoLaboratory of Molecular Neurobiology, Department of Neuroscience, IRCCS - Istituto di Ricerche Farmacologiche Mario Negri, Via La Masa 19, 20156, Milan, Italy. giovanni.nardo@marionegri.it.ORCID 0000-0002-1803-1484
Maria Chiara TroleseLaboratory of Molecular Neurobiology, Department of Neuroscience, IRCCS - Istituto di Ricerche Farmacologiche Mario Negri, Via La Masa 19, 20156, Milan, Italy.
Mattia VerderioLaboratory of Molecular Neurobiology, Department of Neuroscience, IRCCS - Istituto di Ricerche Farmacologiche Mario Negri, Via La Masa 19, 20156, Milan, Italy.
Alessandro MarianiLaboratory of Analytical Biochemistry, Department of Environmental Health Sciences, IRCCS - Istituto di Ricerche Farmacologiche Mario Negri, Via La Masa 19, 20156, Milan, Italy.
Massimiliano de PaolaLaboratory of Analytical Biochemistry, Department of Environmental Health Sciences, IRCCS - Istituto di Ricerche Farmacologiche Mario Negri, Via La Masa 19, 20156, Milan, Italy.
Nilo RivaNeuropathology Unit, Department of Neurology, INSPE- San Raffaele Scientific Institute, Dibit II, Via Olgettina 48, 20132, Milan, Italy.
Giorgia DinaNeuropathology Unit, Department of Neurology, INSPE- San Raffaele Scientific Institute, Dibit II, Via Olgettina 48, 20132, Milan, Italy.
Nicolò PaniniLaboratory of Cancer Pharmacology Department of Oncology, Flow Cytometry Unit, IRCCS - Istituto di Ricerche Farmacologiche Mario Negri, via La Masa 19, 20156, Milan, Italy.
Eugenio ErbaLaboratory of Cancer Pharmacology Department of Oncology, Flow Cytometry Unit, IRCCS - Istituto di Ricerche Farmacologiche Mario Negri, via La Masa 19, 20156, Milan, Italy.
Angelo QuattriniNeuropathology Unit, Department of Neurology, INSPE- San Raffaele Scientific Institute, Dibit II, Via Olgettina 48, 20132, Milan, Italy.
Caterina BendottiLaboratory of Molecular Neurobiology, Department of Neuroscience, IRCCS - Istituto di Ricerche Farmacologiche Mario Negri, Via La Masa 19, 20156, Milan, Italy.
Mario Negri Institute for Pharmacological Research · IT

Funding

FP7 Ideas: European Research Council 259867Regione Lombardia 2015-0023
6 · The paper itself

Abstract

backgroundThe major histocompatibility complex I (MHCI) is a key molecule for the interaction of mononucleated cells with CD8

methodsTo assess the role of MHCI in the disease, we examined transgenic SOD1

resultsThe lack of MHCI and CD8

conclusionsWe provided straightforward evidence for a dual role of MHCI in the peripheral nervous system (PNS) compared to the CNS, pointing out regional and temporal differences in the clinical responses of ALS mice. These findings offer a possible explanation for the failure of systemic immunomodulatory treatments and suggest new potential strategies to prevent the progression of ALS.

Indexed as

Amyotrophic Lateral SclerosisAnimalsCD8-Positive T-LymphocytesDisease Models, AnimalDisease ProgressionHistocompatibility Antigens Class IMiceMice, Inbred C57BLMice, TransgenicPeripheral Nervous SystemSpinal CordHistocompatibility Antigens Class IAmyotrophic lateral sclerosisCD8+ T cellsMHCIMotor neuronNeuroinflammationPeripheral nervous systemSOD1G93A mice

Identifiers

PMID30092791
PMCPMC6085701
OpenAlexW2887947540

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.