Evidence map›Paper›PMID 32620788›Full record

ArticleCellular & molecular immunology2021

ERMAP is a B7 family-related molecule that negatively regulates T cell and macrophage responses.

Min Su, Yujun Lin, Cheng Cui, Xiaohong Tian, Laijun Lai

Open access · bronzeAbstract read
In one paragraph

Article in Cellular & molecular immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
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

5 authors at 1 institution in 2 countries.

Min SuDepartment of Human Histology and Embryology, School of Basic Medical Sciences, Stem Cell and Tissue Engineering Research Centre, Guizhou Medical University, Guiyang, Guizhou, China.ORCID http://orcid.org/0000-0002-6922-6281
Yujun LinDepartment of Allied Health Sciences, University of Connecticut, Storrs, CT, USA.ORCID http://orcid.org/0000-0002-8937-1259
Cheng CuiDepartment of Allied Health Sciences, University of Connecticut, Storrs, CT, USA.
Xiaohong TianDepartment of Allied Health Sciences, University of Connecticut, Storrs, CT, USA.
Laijun LaiDepartment of Allied Health Sciences, University of Connecticut, Storrs, CT, USA. laijun.lai@uconn.edu.ORCID http://orcid.org/0000-0002-4581-7642
University of Connecticut · US

Funding

Transplantation of ESC-derived thymic epithelial progenitors expressing autoantigen(s) ameliorating experimental autoimmune encephalomyelitisR01AI123131 · NIAID · UNIVERSITY OF CONNECTICUT STORRS · PI LAI, LAIJUN · 2016 to 2020
$1.9M
Connecticut Innovations (Connecticut Innovations Incorporated) 16-RMB-UCONN-02NIAID NIH HHS R01 AI123131
6 · The paper itself

Abstract

T cell activation and tolerance are tightly regulated by costimulatory and coinhibitory molecules. B7 family members play a crucial role in regulating immune responses. In this study, we identified erythroid membrane-associated protein (ERMAP) as a novel T cell inhibitory molecule. ERMAP shares significant sequence and structural homology with existing B7 family members in its extracellular domain. The ERMAP protein is expressed on the cell surface of resting and activated antigen-presenting cells (APCs) and in some tumor tissues. The putative ERMAP receptor is expressed on activated CD4 and CD8 T cells and macrophages. Both mouse and human ERMAP-IgG2a Fc (ERMAP-Ig) fusion proteins inhibit T cell functions in vitro. Administration of ERMAP-Ig protein ameliorates autoimmune diseases, including experimental autoimmune encephalomyelitis and type 1 diabetes, in mice. Anti-ERMAP antibody enhances macrophage phagocytosis of cancer cells in vitro. Furthermore, administration of an anti-ERMAP antibody inhibits tumor growth in mice likely by blocking the inhibitory effects of ERMAP on T cells and macrophages. Our results suggest that therapeutic interaction with the ERMAP inhibitory pathway may represent a novel strategy for treating patients with autoimmune disease or cancer.

Indexed as

Blood Group AntigensButyrophilinsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesLymphocyte ActivationMacrophagesAnimalsAntigen-Presenting CellsB7-1 AntigenEncephalomyelitis, Autoimmune, ExperimentalHumansMembrane ProteinsMiceB7-1 AntigenBlood Group AntigensButyrophilinsErmap protein, mouseMembrane Proteinsscianna antigensautoimmunityEAET cell inhibitory moleculesT cells

Identifiers

PMID32620788
PMCPMC8322165
OpenAlexW3038847033

What OpenQuestion holds

Textmetadata
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.