Evidence map›Paper›PMID 36651994›Full record

ArticleCellular and molecular life sciences : CMLS2023

Detection of antibodies against the huntingtin protein in human plasma.

Hélèna L Denis, Melanie Alpaugh, Claudia P Alvarez, Alexis Fenyi, Roger A Barker, Sylvain Chouinard, Cheryl H Arrowsmith, Ronald Melki, Richard Labib, Rachel J Harding and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Do human B-1 lymphocytes truly exist?Frontiers in immunology · 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

11 authors at 6 institutions in 3 countries.

Hélèna L DenisCentre de Recherche du CHU de Québec, Axe Neurosciences, T2-07, 2705, Boulevard Laurier, Québec, QC, G1V 4G2, Canada.
Melanie AlpaughCentre de Recherche du CHU de Québec, Axe Neurosciences, T2-07, 2705, Boulevard Laurier, Québec, QC, G1V 4G2, Canada.
Claudia P AlvarezStructural Genomics Consortium, University of Toronto, MaRS Building Suite 700, 101 College Street, Toronto, ON, M5G1L7, Canada.
Alexis FenyiLaboratory of Neurodegenerative Diseases, Institut François Jacob, MIRCen, CEA, CNRS, Fontenay-Aux-Roses, France.
Roger A BarkerJohn van Geest Center for Brain Repair, University of Cambridge, Cambridge, UK.
Sylvain ChouinardCentre Hospitalier Universitaire de Montréal-Hôtel Dieu, Movement Disorders Unit, CHUM, Montréal, QC, Canada.
Cheryl H ArrowsmithStructural Genomics Consortium, University of Toronto, MaRS Building Suite 700, 101 College Street, Toronto, ON, M5G1L7, Canada.
Ronald MelkiLaboratory of Neurodegenerative Diseases, Institut François Jacob, MIRCen, CEA, CNRS, Fontenay-Aux-Roses, France.
Richard LabibDepartment of Mathematical and Industrial Engineering, Polytechnique Montréal, Montréal, QC, Canada.
Rachel J HardingStructural Genomics Consortium, University of Toronto, MaRS Building Suite 700, 101 College Street, Toronto, ON, M5G1L7, Canada. rachel.harding@utoronto.ca.
Francesca CicchettiCentre de Recherche du CHU de Québec, Axe Neurosciences, T2-07, 2705, Boulevard Laurier, Québec, QC, G1V 4G2, Canada. francesca.cicchetti@crchudequebec.ulaval.ca.ORCID http://orcid.org/0000-0001-5490-1961
University of Toronto · CACentre hospitalier universitaire de Québec · CACentre National de la Recherche Scientifique · FRCentre intégré universitaire de santé et de services sociaux de la Mauricie-et-du-Centre-du-Québec · CAPolytechnique Montréal · CAUniversity of Cambridge · GB

Funding

CIHR PJT-168865Fonds de Recherche du Québec - Santé 28941Wellcome Trust
6 · The paper itself

Abstract

Huntington's disease (HD) is a dominantly inherited neurodegenerative disorder resulting from a CAG expansion in the huntingtin (HTT) gene, which leads to the production and accumulation of mutant huntingtin (mHTT). While primarily considered a disorder of the central nervous system, multiple changes have been described to occur throughout the body, including activation of the immune system. In other neurodegenerative disorders, activation of the immune system has been shown to include the production of antibodies against disease-associated pathological proteins. However, the existence of mHTT-targeted antibodies has never been reported. In this study, we assessed the presence and titer of antibodies recognizing HTT/mHTT in patients with HD (n = 66) and age- and gender-matched healthy controls (n = 66) using a combination of Western blotting and ELISA. Together, these analyses revealed that antibodies capable of recognizing HTT/mHTT were detectable in the plasma samples of all participants, including healthy controls. When antibody levels were monitored at different disease stages, it was observed that antibodies against full-length mHTT were highest in patients with severe disease while antibodies against HTTExon1 were elevated in patients with mild disease. Combined, these results suggest that antibodies detecting different forms of mHTT peak at different disease stages.

Indexed as

Huntington DiseaseNeurodegenerative DiseasesAntibodiesHumansHuntingtin ProteinAntibodiesHuntingtin ProteinAntibodiesHuman samplesHuntingtin proteinHuntington’s diseasePlasma

Identifiers

PMID36651994
PMCPMC9849309
OpenAlexW4317213615

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.