Evidence map›Paper›PMID 38612581›Full record

ArticleInternational journal of molecular sciences2024

Anti-LAMP-2 Antibody Seropositivity in Children with Primary Systemic Vasculitis Affecting Medium- and Large-Sized Vessels.

Tayfun Hilmi Akbaba, Kirandeep K Toor, Simranpreet K Mann, Kristen M Gibson, Gabriel Alejandro Alfaro, Banu Balci-Peynircioglu, David A Cabral, Kimberly A Morishita, Kelly L Brown, PedVas Investigator’s Network

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 93% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 3 institutions in 3 countries.

Tayfun Hilmi AkbabaBC Children's Hospital Research Institute, Vancouver, BC V5Z 4H4, Canada.ORCID 0000-0002-3875-5244
Kirandeep K ToorBC Children's Hospital Research Institute, Vancouver, BC V5Z 4H4, Canada.
Simranpreet K MannBC Children's Hospital Research Institute, Vancouver, BC V5Z 4H4, Canada.ORCID 0009-0000-8086-3604
Kristen M GibsonBC Children's Hospital Research Institute, Vancouver, BC V5Z 4H4, Canada.
Gabriel Alejandro AlfaroMeso Scale Diagnostics, LLC, Rockville, MD 20850, USA.
Banu Balci-PeynirciogluDepartment of Medical Biology, Faculty of Medicine, Hacettepe University, 06800 Ankara, Turkey.
David A CabralBC Children's Hospital Research Institute, Vancouver, BC V5Z 4H4, Canada.
Kimberly A MorishitaBC Children's Hospital Research Institute, Vancouver, BC V5Z 4H4, Canada.
Kelly L BrownBC Children's Hospital Research Institute, Vancouver, BC V5Z 4H4, Canada.ORCID 0000-0001-5385-3582
PedVas Investigator’s Network
University of British Columbia · CAHacettepe University · TRMeso Scale Discovery (United States) · US

Funding

CIHR PJT-180302CIHR TR2-119188
6 · The paper itself

Abstract

Chronic primary systemic vasculitis (PSV) comprises a group of heterogeneous diseases that are broadly classified by affected blood vessel size, clinical traits and the presence (or absence) of anti-neutrophil cytoplasmic antibodies (ANCA) against proteinase 3 (PR3) and myeloperoxidase (MPO). In small vessel vasculitis (SVV), ANCA are not present in all patients, and they are rarely detected in patients with vasculitis involving medium (MVV) and large (LVV) blood vessels. Some studies have demonstrated that lysosome-associated membrane protein-2 (LAMP-2/CD107b) is a target of ANCA in SVV, but its presence and prognostic value in childhood MVV and LVV is not known. This study utilized retrospective sera and clinical data obtained from 90 children and adolescents with chronic PSV affecting small (SVV, n = 53), medium (MVV, n = 16), and large (LVV, n = 21) blood vessels. LAMP-2-ANCA were measured in time-of-diagnosis sera using a custom electrochemiluminescence assay. The threshold for seropositivity was established in a comparator cohort of patients with systemic autoinflammatory disease. The proportion of LAMP-2-ANCA-seropositive individuals and sera concentrations of LAMP-2-ANCA were assessed for associations with overall and organ-specific disease activity at diagnosis and one-year follow up. This study demonstrated a greater time-of-diagnosis prevalence and sera concentration of LAMP-2-ANCA in MVV (52.9% seropositive) and LVV (76.2%) compared to SVV (45.3%). Further, LAMP-2-ANCA-seropositive individuals had significantly lower overall, but not organ-specific, disease activity at diagnosis. This did not, however, result in a greater reduction in disease activity or the likelihood of achieving inactive disease one-year after diagnosis. The results of this study demonstrate particularly high prevalence and concentration of LAMP-2-ANCA in chronic PSV that affects large blood vessels and is seronegative for traditional ANCA. Our findings invite reconsideration of roles for autoantigens other than MPO and PR3 in pediatric vasculitis, particularly in medium- and large-sized blood vessels.

Indexed as

Systemic VasculitisAdolescentAntibodies, Antineutrophil CytoplasmicAutoantigensChildHumansMyeloblastinRetrospective StudiesAntibodies, Antineutrophil CytoplasmicAutoantigensMyeloblastinanti-neutrophil cytoplasmic antibodiesautoantibodieschildhood-onset primary vasculitislysosome-associated membrane protein-2polyarteritis nodosaTakayasu’s arteritis

Identifiers

PMID38612581
PMCPMC11011342
OpenAlexW4393278706

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.