Evidence map›Paper›PMID 28760953›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

CD318 is a ligand for CD6.

Gospel Enyindah-Asonye, Yan Li, Jeffrey H Ruth, Danislav S Spassov, Katie E Hebron, Andries Zijlstra, Mark M Moasser, Benlian Wang, Nora G Singer, Huadong Cui and 4 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04708444 (Prognostic Value of CD318 in Acute Myeloid Leukemia Patients at Assiut University Hospital), which is not on this map. Cited by 77 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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.

NCT04708444 unknown statusnot on this mapstarted 2021, after this paper: background citation

Prognostic Value of CD318 in Acute Myeloid Leukemia Patients at Assiut University Hospital

TypeobservationalSponsorShimaa Arafa IbrahimRan2021 to 2023Enrolled100ConditionsAcute Myeloid LeukemiaArmsCD318
3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 1 synthesis or guideline pooled it, 94 citations in OpenAlex.

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  16. The OT-II model reveals dualFrontiers in immunology · 2025
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17 more citing papers are in PubMed but not listed here.

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

14 authors at 7 institutions in 2 countries.

Gospel Enyindah-AsonyeDepartment of Immunology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195.
Yan LiDepartment of Immunology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195.ORCID 0000-0002-7058-3569
Jeffrey H RuthDivision of Rheumatology and Clinical Autoimmunity Center of Excellence, University of Michigan, Ann Arbor, MI 48109.
Danislav S SpassovDepartment of Medicine and Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA 94143.
Katie E HebronDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University, Nashville, TN 37240.
Andries ZijlstraDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University, Nashville, TN 37240.
Mark M MoasserDepartment of Medicine and Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA 94143.
Benlian WangCenter for Proteomics and Bioinformatics, Case Western Reserve University, Cleveland, OH 44106.
Nora G SingerDivision of Rheumatology, MetroHealth Medical Center, Cleveland, OH 44109.
Huadong CuiDivision of Rheumatology and Clinical Autoimmunity Center of Excellence, University of Michigan, Ann Arbor, MI 48109.
Ray A OharaDivision of Rheumatology and Clinical Autoimmunity Center of Excellence, University of Michigan, Ann Arbor, MI 48109.
Stephanie M RasmussenDivision of Rheumatology and Clinical Autoimmunity Center of Excellence, University of Michigan, Ann Arbor, MI 48109.
David A FoxDivision of Rheumatology and Clinical Autoimmunity Center of Excellence, University of Michigan, Ann Arbor, MI 48109; dfox@umich.edu linf2@ccf.org.ORCID 0000-0002-0230-6607
Feng LinDepartment of Immunology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195; dfox@umich.edu linf2@ccf.org.
University of Michigan · USCleveland Clinic Lerner College of Medicine · USUniversity of California, San Francisco · USVanderbilt University · USCase Western Reserve University · USMetroHealth · USSichuan University · CN

Funding

MULTIDISCIPLINARY BASIC RESEARCH TRAINING IN CANCERT32CA009592 · NCI · VANDERBILT UNIVERSITY · PI Justin M Balko, Julie A Rhoades (Sterling) · 1987 to 2026
$10.4M
Role of CD6 in the pathogenesis of autoimmune uveitisR01EY025373 · NEI · CLEVELAND CLINIC LERNER COM-CWRU · PI LIN, FENG C · 2017 to 2021
$2.0M
Tetraspanin-mediated regulation of tumor cell migration and metastasisR01CA143081 · NCI · VANDERBILT UNIVERSITY · PI ZIJLSTRA, ANDRIES · 2010 to 2014
$1.5M
Complement and OsteoporosisR01AR061564 · NIAMS · CLEVELAND CLINIC LERNER COM-CWRU · PI DENNIS, JAMES E, LIN, FENG C · 2012 to 2015
$1.5M
University of Michigan Clinical Autoimmunity Center of ExcellenceUM1AI144298 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FOX, DAVID ALAN, KHANNA, DINESH · 2019 to 2023
$546k
University of Michigan Autoimmunity Center of Excellence, Clinical Research ProgrUM1AI110557 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FOX, DAVID ALAN · 2014 to 2018
$543k
Regulation of prostate cancer progression by ALCAM proteolysisF31CA189764 · NCI · VANDERBILT UNIVERSITY · PI HEBRON, KATIE ELIZABETH · 2014 to 2016
$76k
NCI NIH HHS F31 CA189764NCI NIH HHS R01 CA143081NCI NIH HHS T32 CA009592NEI NIH HHS R01 EY025373NIAID NIH HHS UM1 AI110557NIAMS NIH HHS R01 AR061564
6 · The paper itself

Abstract

It has been proposed that CD6, an important regulator of T cells, functions by interacting with its currently identified ligand, CD166, but studies performed during the treatment of autoimmune conditions suggest that the CD6-CD166 interaction might not account for important functions of CD6 in autoimmune diseases. The antigen recognized by mAb 3A11 has been proposed as a new CD6 ligand distinct from CD166, yet the identity of it is hitherto unknown. We have identified this CD6 ligand as CD318, a cell surface protein previously found to be present on various epithelial cells and many tumor cells. We found that, like CD6 knockout (KO) mice, CD318 KO mice are also protected in experimental autoimmune encephalomyelitis. In humans, we found that CD318 is highly expressed in synovial tissues and participates in CD6-dependent adhesion of T cells to synovial fibroblasts. In addition, soluble CD318 is chemoattractive to T cells and levels of soluble CD318 are selectively and significantly elevated in the synovial fluid from patients with rheumatoid arthritis and juvenile inflammatory arthritis. These results establish CD318 as a ligand of CD6 and a potential target for the diagnosis and treatment of autoimmune diseases such as multiple sclerosis and inflammatory arthritis.

Indexed as

A549 CellsAnimalsAntigens, CDAntigens, Differentiation, T-LymphocyteAntigens, NeoplasmArthritis, RheumatoidCell Adhesion MoleculesCell LineCell Line, TumorEncephalomyelitis, Autoimmune, ExperimentalHumansLigandsMembrane GlycoproteinsMice, Inbred C57BLMice, KnockoutNeoplasm ProteinsAntigens, CDAntigens, Differentiation, T-LymphocyteAntigens, NeoplasmCD6 antigenCDCP1 protein, humanCDCP1 protein, mouseCell Adhesion MoleculesLigandsMembrane GlycoproteinsNeoplasm ProteinsautoimmunityCD318CD6ligandT cell

Identifiers

PMID28760953
PMCPMC5565428
OpenAlexW2740862211

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.