Evidence map›Paper›PMID 15027906›Full record

ArticleImmunology2004

Cloning and characterization of an immunoglobulin A Fc receptor from cattle.

H Craig Morton, Richard J Pleass, Anne K Storset, Erik Dissen, John L Williams, Per Brandtzaeg, Jenny M Woof

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.1field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

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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

7 authors at 5 institutions in 2 countries.

H Craig MortonLaboratory of Immunohistochemistry and Immunopathology (LIIPAT), Institute of Pathology, University of Oslo, Rikshospitalet, Oslo, Norway. craig.morton@labmed.uio.no
Richard J Pleass
Anne K Storset
Erik Dissen
John L Williams
Per Brandtzaeg
Jenny M Woof
Oslo University Hospital · NOUniversity of Dundee · GBNorwegian University of Life Sciences · NORoslin Institute · GBUniversity of Oslo · NO

Funding

Biotechnology and Biological Sciences Research Council G18276Medical Research Council G0300145Wellcome Trust
6 · The paper itself

Abstract

Here, we describe the cloning, sequencing and characterization of an immunoglobulin A (IgA) Fc receptor from cattle (bFcalphaR). By screening a translated EST database with the protein sequence of the human IgA Fc receptor (CD89) we identified a putative bovine homologue. Subsequent polymerase chain reaction (PCR) amplification confirmed that the identified full-length cDNA was expressed in bovine cells. COS-1 cells transfected with a plasmid containing the cloned cDNA bound to beads coated with either bovine or human IgA, but not to beads coated with bovine IgG2 or human IgG. The bFcalphaR cDNA is 873 nucleotides long and is predicted to encode a 269 amino-acid transmembrane glycoprotein composed of two immunoglobulin-like extracellular domains, a transmembrane region and a short cytoplasmic tail devoid of known signalling motifs. Genetically, bFcalphaR is more closely related to CD89, bFcgamma2R, NKp46, and the KIR and LILR gene families than to other FcRs. Moreover, the bFcalphaR gene maps to the bovine leucocyte receptor complex on chromosome 18. Identification of the bFcalphaR will aid in the understanding of IgA-FcalphaR interactions, and may facilitate the isolation of FcalphaR from other species.

Indexed as

Amino Acid SequenceAnimalsAntigens, CDBase SequenceCattleChlorocebus aethiopsChromosome MappingCloning, MolecularCOS CellsDNA, ComplementaryHumansLigandsMolecular Sequence DataPhylogenyReceptors, FcSequence AlignmentAntigens, CDDNA, ComplementaryFc(alpha) receptorLigandsReceptors, Fc

Identifiers

PMID15027906
PMCPMC1782410
OpenAlexW2036676930

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.