Evidence map›Paper›PMID 26927797›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

Alternatively Activated Macrophages Boost Induced Regulatory T and Th17 Cell Responses during Immunotherapy for Colitis.

Dipica Haribhai, Jennifer Ziegelbauer, Shuang Jia, Kyle Upchurch, Ke Yan, Erica G Schmitt, Nita H Salzman, Pippa Simpson, Martin J Hessner, Talal A Chatila and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.7field-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

32 citing papers in PubMed, 49 citations in OpenAlex.

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  10. Recruited CD68Bioactive materials · 2021
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  17. Dietary Supplementation with Sea Bass (International journal of molecular sciences · 2019
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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

11 authors at 2 institutions in 1 country.

Dipica HaribhaiSection of Rheumatology, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI 53226;
Jennifer ZiegelbauerSection of Rheumatology, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI 53226;
Shuang JiaSection of Endocrinology, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI 53226;
Kyle UpchurchSection of Rheumatology, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI 53226;
Ke YanSection of Quantitative Health Sciences, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI 53226;
Erica G SchmittSection of Rheumatology, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI 53226;
Nita H SalzmanSection of Gastroenterology, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI 53226; and.
Pippa SimpsonSection of Quantitative Health Sciences, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI 53226;
Martin J HessnerSection of Endocrinology, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI 53226;
Talal A ChatilaDivision of Immunology, Children's Hospital Boston, Boston, MA 02115.
Calvin B WilliamsSection of Rheumatology, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI 53226; cwilliam@mcw.edu.
Medical College of Wisconsin · USBoston Children's Hospital · US

Funding

Mechanisms of Disease Pathogenesis in Regulatory T cell DeficiencyR01AI085090 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHATILA, TALAL AMINE, WILLIAMS, CALVIN B · 2010 to 2020
$3.9M
Regulatory T Cell Selection and SpecificityR01AI073731 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI CHATILA, TALAL AMINE, WILLIAMS, CALVIN B · 2009 to 2010
$986k
NIAID NIH HHS R01 AI073731NIAID NIH HHS R01 AI085090
6 · The paper itself

Abstract

Induced regulatory T (iTreg) and Th17 cells promote mucosal homeostasis. We used a T cell transfer model of colitis to compare the capacity of iTreg and Th17 cells to develop in situ following the transfer of naive CD4(+)CD45RB(hi)T cells intoRag1(-/-)C57BL/6 or BALB/c mice, the prototypical Th1/M1- and Th2/M2-prone strains. We found that the frequency and number of Foxp3(+)iTreg cells and Th17 cells were significantly reduced in C57BL/6 mice compared with the BALB/c strain. C57BL/6 mice with colitis were also resistant to natural Treg cell immunotherapy. Pretreatment of C57BL/6Rag1(-/-)mice with IL-4 plus IL-13, or with M2a but not M1 macrophages, dramatically increased the generation of iTreg and Th17 cells. Importantly, M2a transfers, either as a pretreatment or in mice with established colitis, allowed successful immunotherapy with natural Treg cells. M2a macrophages also reduced the generation of pathogenic iTreg cells that lost Foxp3 expression, suggesting that they stabilize the expression of Foxp3. Thus, polarized M2a macrophages drive a directionally concordant expansion of the iTreg-Th17 cell axis and can be exploited as a therapeutic adjuvant in cell-transfer immunotherapy to re-establish mucosal tolerance.

Indexed as

AnimalsColitisForkhead Transcription FactorsImmune ToleranceImmunotherapy, AdoptiveInterleukin-13Interleukin-4Macrophage ActivationMacrophagesMiceMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutTh17 CellsT-Lymphocytes, RegulatoryForkhead Transcription FactorsFoxp3 protein, mouseInterleukin-13Interleukin-4

Identifiers

PMID26927797
PMCPMC4851766
OpenAlexW2341277212

What OpenQuestion holds

Textmetadata
LicenceTDM
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.