Evidence map›Paper›PMID 1940803›Full record

ArticleThe Journal of experimental medicine1991

Identification of C3 beta chain as the human serum eosinophil cytotoxicity inhibitor.

M S Minkoff, W W Wong, D S Silberstein

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 1991. 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
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

3 authors.

M S MinkoffDepartment of Rheumatology and Immunology, Brigham and Women's Hospital, Boston, Massachusetts.
W W Wong
D S Silberstein

Funding

IMMUNOLOGIC BASIS OF RESISTANCE AND HYPERSENSITIVITYT32AI007306 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI Nora Amanda Barrett, Joshua A Boyce · 1985 to 2026
$12.2M
STRUCTURE AND BIOLOGICAL FUNCTION OF THE MONOKINE ECEFR29AI028525 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI SILBERSTEIN, DAVID S. · 1989 to 1993
–
NIAID NIH HHS AI-07306NIAID NIH HHS AI-22532NIAID NIH HHS AI-28525
6 · The paper itself

Abstract

An eosinophil cytotoxicity inhibitor (ECI) was purified from serum of a human subject with severe allergic dermatitis. Molecular weight of the isolated polypeptide (75,000) and its NH2-terminal amino acid sequence identified it as the beta chain of the C3 complement component (apparently free, but perhaps attached to very small fragments of the alpha chain). Free beta chain, prepared from normal plasma by reduction of C3, inhibited both eosinophil cytotoxicity and neutrophil adherence functions, with half-maximal activity at approximately 250 ng/ml. Apparently free C3 beta chain was detected in certain human biological fluids associated with inflammation; the presence of C3 beta chain correlated with ECI activity. This evidence demonstrates a potential role for free C3 beta chain as a suppressor of eosinophil and neutrophil functions in inflammation.

Indexed as

Amino Acid SequenceComplement C3Cytotoxicity, ImmunologicDermatitis, ContactEosinophilsHumansIn Vitro TechniquesMolecular Sequence DataMolecular WeightComplement C3

Identifiers

PMID1940803
PMCPMC2118984

What OpenQuestion holds

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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.