Evidence map›Paper›PMID 19363291›Full record

ArticleThe Journal of clinical investigation2009

Oxidation-specific epitopes are dominant targets of innate natural antibodies in mice and humans.

Meng-Yun Chou, Linda Fogelstrand, Karsten Hartvigsen, Lotte F Hansen, Douglas Woelkers, Peter X Shaw, Jeomil Choi, Thomas Perkmann, Fredrik Bäckhed, Yury I Miller and 4 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 281 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
281citing papers in PubMed, 1 pooled it
10.0field-weighted citation impact, top 1% 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

281 citing papers in PubMed, 1 synthesis or guideline pooled it, 460 citations in OpenAlex.

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  11. Mitigating atherosclerosis: Integrating vaccines with gene targets.American heart journal plus : cardiology research and practice · 2025
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221 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 1 institution in 1 country.

Meng-Yun ChouDepartment of Medicine, UCSD, La Jolla, California 92093, USA.
Linda Fogelstrand
Karsten Hartvigsen
Lotte F Hansen
Douglas Woelkers
Peter X Shaw
Jeomil Choi
Thomas Perkmann
Fredrik Bäckhed
Yury I Miller
Sohvi Hörkkö
Maripat Corr
Joseph L Witztum
Christoph J Binder
University of California San Diego · US

Funding

Transcriptional GenomicsP01HL088093 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WITZTUM, JOSEPH L. · 2008 to 2018
$26.4M
SCOR IN MOLECULAR MEDICINE AND ATHEROSCLEROSISP50HL056989 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI QUEHENBERGER, OSWALD · 1997 to 2006
$14.1M
Development of a Vaccine Approach to Inhibit AtherosclerosisR01HL086559 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WITZTUM, JOSEPH L. · 2007 to 2011
$2.0M
NHLBI NIH HHS HL086559NHLBI NIH HHS P01 HL088093NHLBI NIH HHS P50 HL056989NHLBI NIH HHS R01 HL086559
6 · The paper itself

Abstract

Atherosclerosis is a chronic inflammatory disease characterized by the accumulation of oxidized lipoproteins and apoptotic cells. Adaptive immune responses to various oxidation-specific epitopes play an important role in atherogenesis. However, accumulating evidence suggests that these epitopes are also recognized by innate receptors, such as scavenger receptors on macrophages, and plasma proteins, such as C-reactive protein (CRP). Here, we provide multiple lines of evidence that oxidation-specific epitopes constitute a dominant, previously unrecognized target of natural Abs (NAbs) in both mice and humans. Using reconstituted mice expressing solely IgM NAbs, we have shown that approximately 30% of all NAbs bound to model oxidation-specific epitopes, as well as to atherosclerotic lesions and apoptotic cells. Because oxidative processes are ubiquitous, we hypothesized that these epitopes exert selective pressure to expand NAbs, which in turn play an important role in mediating homeostatic functions consequent to inflammation and cell death, as demonstrated by their ability to facilitate apoptotic cell clearance. These findings provide novel insights into the functions of NAbs in mediating host homeostasis and into their roles in health and diseases, such as chronic inflammatory diseases and atherosclerosis.

Indexed as

Adoptive TransferAnimalsAntibody AffinityAntibody FormationAntibody SpecificityApoptosisAtherosclerosisB-Lymphocyte SubsetsEpitopesFemaleFetal BloodGerm-Free LifeHomeodomain ProteinsImmunity, InnateImmunoglobulin MLipoproteins, LDLEpitopesHomeodomain ProteinsImmunoglobulin MLipoproteins, LDLMalondialdehydemalondialdehyde-low density lipoprotein, mouseoxidized low density lipoproteinPhosphorylcholinephosphorylcholine-bovine serum albuminRAG-1 proteinReceptors, LDLSerum Albumin, Bovine

Identifiers

PMID19363291
PMCPMC2673862
OpenAlexW2125661827

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.