Evidence map›Paper›PMID 38877178›Full record

ArticleNature immunology2024

Genetic and environmental interactions contribute to immune variation in rewilded mice.

Oyebola Oyesola, Alexander E Downie, Nina Howard, Ramya S Barre, Kasalina Kiwanuka, Kimberly Zaldana, Ying-Han Chen, Arthur Menezes, Soo Ching Lee, Joseph Devlin and 7 more

Abstract read
In one paragraph

Article in Nature immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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  17. Social association predicts immunological similarity in rewilded mice.bioRxiv : the preprint server for biology · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

Oyebola Oyesola *Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA. oyebola.oyesola@nih.gov.ORCID http://orcid.org/0000-0002-5347-7502
Alexander E Downie *Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, USA.ORCID http://orcid.org/0000-0002-6743-620X
Nina HowardLaboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.ORCID http://orcid.org/0000-0002-1204-5885
Ramya S BarreDepartment of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, USA.ORCID http://orcid.org/0000-0002-8773-6349
Kasalina KiwanukaLaboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Kimberly ZaldanaLaboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Ying-Han ChenKimmel Center for Biology and Medicine at the Skirball Institute, New York University, Grossman School of Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0002-6720-8610
Arthur MenezesDepartment of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, USA.ORCID http://orcid.org/0000-0002-0195-4071
Soo Ching LeeLaboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.ORCID http://orcid.org/0000-0002-5454-2265
Joseph DevlinKimmel Center for Biology and Medicine at the Skirball Institute, New York University, Grossman School of Medicine, New York, NY, USA.
Octavio Mondragón-PalominoLaboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Camila Oliveira Silva SouzaLaboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.ORCID http://orcid.org/0000-0002-6922-5270
Christin HerrmannKimmel Center for Biology and Medicine at the Skirball Institute, New York University, Grossman School of Medicine, New York, NY, USA.
Sergei B KoralovDepartment of Pathology, New York University, Grossman School of Medicine, New York, NY, USA.
Ken CadwellDivision of Gastroenterology and Hepatology, Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0002-5860-0661
Andrea L GrahamDepartment of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, USA. algraham@princeton.edu.ORCID http://orcid.org/0000-0002-6580-2755
P'ng LokeLaboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA. png.loke@nih.gov.ORCID http://orcid.org/0000-0002-6211-3292

Funding

New Jersey Alliance for Clinical Translational Science: NJ ACTSUL1TR003017 · NCATS · RUTGERS BIOMEDICAL/HEALTH SCIENCES-RBHS · PI PANETTIERI, REYNOLD ALEXANDER · 2019 to 2023
$28.9M
Regulation of mucosal immune responses by helminth infectionsZIAAI001255 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI LOKE, P'NG · 2020 to 2025
$6.1M
Interactions between helminth colonization and the gut microbiotaR01AI130945 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CADWELL, KEN HASHIGIWA · 2018 to 2022
$3.3M
Role of S.aureus in Cutaneous T Cell Lymphoma PathogenesisR01CA271245 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Sergei Borisovich Koralov · 2022 to 2026
$2.7M
Investigating reprogramming of the immune system by parasitic helminths and environmental antigensZIAAI001386 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI OYESOLA, OYEBOLA · 2024 to 2025
$2.3M
Interactions between Trichuris and the gut microbiotaR01AI179896 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI Ken Hashigiwa Cadwell, E. Jane Albert Hubbard · 2024 to 2026
$2.0M
National Science Foundation (NSF) # DGE-2039656NCATS NIH HHS UL1 TR003017NCI NIH HHS R01 CA271245NIAID NIH HHS R01 AI130945NIAID NIH HHS R01 AI179896U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R01: CS271245
6 · The paper itself

Abstract

The relative and synergistic contributions of genetics and environment to interindividual immune response variation remain unclear, despite implications in evolutionary biology and medicine. Here we quantify interactive effects of genotype and environment on immune traits by investigating C57BL/6, 129S1 and PWK/PhJ inbred mice, rewilded in an outdoor enclosure and infected with the parasite Trichuris muris. Whereas cellular composition was shaped by interactions between genotype and environment, cytokine response heterogeneity including IFNγ concentrations was primarily driven by genotype with consequence on worm burden. In addition, we show that other traits, such as expression of CD44, were explained mostly by genetics on T cells, whereas expression of CD44 on B cells was explained more by environment across all strains. Notably, genetic differences under laboratory conditions were decreased following rewilding. These results indicate that nonheritable influences interact with genetic factors to shape immune variation and parasite burden.

Indexed as

Gene-Environment InteractionMice, Inbred C57BLTrichuriasisTrichurisAnimalsB-LymphocytesFemaleGenotypeHyaluronan ReceptorsInterferon-gammaMaleMiceT-LymphocytesCd44 protein, mouseHyaluronan ReceptorsInterferon-gamma

Identifiers

PMID38877178
PMCPMC11224019

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.