Evidence map›Paper›PMID 39010674›Full record

ArticleACR open rheumatology2024

Signal Regulatory Protein α Expression in Systemic Vasculitis.

Shubhasree Banerjee, Eileen Rose, Sandip Panicker, John Dugan, Nader Khalidi, Curry L Koening, Carol A Langford, Paul A Monach, Christian Pagnoux, Carol A McAlear and 2 more

Abstract read
In one paragraph

Article in ACR open rheumatology, 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
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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.

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

12 authors.

Shubhasree BanerjeeUniversity of Pennsylvania, Philadelphia.ORCID https://orcid.org/0000-0003-0903-1949
Eileen RoseElectra Therapeutics, Inc, South San Francisco, California.
Sandip PanickerElectra Therapeutics, Inc, South San Francisco, California.
John DuganInvicro, LLC, Needham, Massachusetts.
Nader KhalidiMcMaster University and St. Joseph's Hospital, Hamilton, Ontario, Canada.
Curry L KoeningUniversity of Texas, Austin.
Carol A LangfordCleveland Clinic, Cleveland, Ohio.
Paul A MonachVA Boston Healthcare System, Boston, Massachusetts.ORCID https://orcid.org/0000-0003-4937-0515
Christian PagnouxUniversity of Toronto and Mount Sinai Hospital, Toronto, Ontario, Canada.
Carol A McAlearUniversity of Pennsylvania, Philadelphia.
Peter A MerkelUniversity of Pennsylvania, Philadelphia.
Vasculitis Clinical Research Consortium

Funding

VCRC-VF FellowshipU54AR057319 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI MERKEL, PETER A · 2009 to 2020
$12.5M
NCRR NIH HHSNIAMS NIH HHS U54 AR057319
6 · The paper itself

Abstract

objectiveSignal regulatory protein α (SIRPα) is found primarily on myeloid cells, including macrophages and neutrophils; binds to CD47; and regulates phagocytosis, antigen presentation, cellular fusion, cell proliferation, and migration. Therefore, SIRPα may be involved in the pathogenesis of autoimmune diseases, including systemic vasculitis. This study aimed to assess SIRPα expression in tissue samples from patients with vasculitis.

methodsImmunohistochemical staining for SIRPα was performed on temporal artery (TA), kidney, and lung biopsy samples from patients with giant cell arteritis (GCA), patients with microscopic polyangiitis (MPA), patients with granulomatosis with polyangiitis (GPA), and patients without vasculitis. A score of SIRPα

resultsA total of 46 samples from patients with different vasculitides (GCA, MPA, and GPA) were included in the study. Tissue samples included TA samples from 15 patients with GCA; kidney samples from 11 and 9 patients with GPA and MPA, respectively; and lung samples from 11 patients with GPA. Most tissue samples from patients with active vasculitis (15 of 15 TA samples, 17 of 20 kidney samples, and 9 of 11 lung samples) showed SIRPα staining. SIRPα staining intensity was less in kidney samples compared to TA and lung samples.

conclusionThis study demonstrates high-level expression of SIRPα in macrophages and monocytes in affected tissue in systemic vasculitis. These findings provide a foundation for further studies exploring the role of the SIRPα-CD47 pathway in the pathogenesis of systemic vasculitis and the potential for the blockade of SIRPα and/or the depletion of SIRPα

Identifiers

PMID39010674
PMCPMC11471941

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