Evidence map›Paper›PMID 37172087›Full record

ArticleScience advances2023

Broad responses to chemical adducts shape the natural antibody repertoire in early infancy.

Shunya Mashiko, Ronzon R Shihab, Sarah B See, Luca G Z Schahadat, Talita F M Aguiar, Poulomi Roy, Fabrice Porcheray, Emmanuel Zorn

Abstract read
In one paragraph

Article in Science advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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  5. Heme disposal inside heart transplants: a trigger for rejection?The Journal of clinical investigation · 2026
    Article
  6. Review
  7. Article
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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

8 authors.

Shunya MashikoColumbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, NY, USA.ORCID 0000-0002-4829-535X
Ronzon R ShihabColumbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, NY, USA.ORCID 0000-0001-5356-5345
Sarah B SeeColumbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, NY, USA.ORCID 0000-0002-4208-317X
Luca G Z SchahadatColumbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, NY, USA.ORCID 0000-0002-2271-0623
Talita F M AguiarColumbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, NY, USA.ORCID 0000-0003-0202-6848
Poulomi RoyColumbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, NY, USA.
Fabrice PorcherayTransplant Center, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Emmanuel ZornColumbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, NY, USA.ORCID 0000-0001-9985-8389

Funding

Innate B cell immunity and antibody-mediated rejection of human kidney allograftsR01AI123342 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Emmanuel Zorn · 2016 to 2026
$3.3M
NIAID NIH HHS R01 AI123342
6 · The paper itself

Abstract

Natural antibodies are an integral part of innate humoral immunity yet their development and polyreactive nature are still enigmatic. Here, we show that characteristic monoclonal natural antibodies recognize common chemical moieties or adducts, supporting the view that polyreactive antibodies may often correspond to anti-adduct antibodies. We next examined the development of immunoglobulin M (IgM) and IgG to 81 ubiquitous adducts from birth to old age. Newborn IgM only reacted to a limited number of consensus determinants. This highly restricted neonatal repertoire abruptly diversified around 6 months of age through the development of antibodies to environmental antigens and age-driven epigenetic modifications. In contrast, the IgG repertoire was diverse across the entire life span. Our studies reveal an unrecognized component of humoral immunity directed to common adducts. These findings set the ground for further investigations into the role of anti-adduct B cell responses in homeostatic functions and pathological conditions.

Indexed as

Antibodies, MonoclonalAntigensHumansImmunoglobulin GImmunoglobulin MInfantInfant, NewbornAntibodies, MonoclonalAntigensImmunoglobulin GImmunoglobulin M

Identifiers

PMID37172087
PMCPMC10181178

What OpenQuestion holds

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LicenceCC BY-NC
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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.