Evidence map›Paper›PMID 40897376›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2025

Adjuvant conditioning enhances neutrophil function while inducing a suppressive peritoneal macrophage phenotype.

Thais Boccia, Victor Fattori, Matheus Deroco Veloso Da Silva, Nathan L Asquith, Weikang Pan, Michael S Rogers, Ivan Zanoni, Alex G Cuenca

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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.

Thais BocciaDepartment of Surgery, Boston Children's Hospital-Harvard Medical School, Boston, MA, United States.
Victor FattoriVascular Biology Program, Department of Surgery, Boston Children's Hospital-Harvard Medical School, Boston, MA, United States.
Matheus Deroco Veloso Da SilvaVascular Biology Program, Department of Surgery, Boston Children's Hospital-Harvard Medical School, Boston, MA, United States.
Nathan L AsquithVascular Biology Program, Department of Surgery, Boston Children's Hospital-Harvard Medical School, Boston, MA, United States.
Weikang PanDepartment of Surgery, Boston Children's Hospital-Harvard Medical School, Boston, MA, United States.
Michael S RogersVascular Biology Program, Department of Surgery, Boston Children's Hospital-Harvard Medical School, Boston, MA, United States.
Ivan ZanoniDivision of Immunology, Division of Gastroenterology, Department of Pediatrics, Boston Children's Hospital-Harvard Medical School, Boston, MA, United States.
Alex G CuencaDepartment of Surgery, Boston Children's Hospital-Harvard Medical School, Boston, MA, United States.ORCID 0000-0002-6219-7035

Funding

Neuroimmune communication as a driver of lesion formation and macrophage colonization of the omentum in endometriosis-associated painK99HD115239 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI FATTORI, VICTOR · 2024 to 2024
$255k
American Pediatric Surgical Association Jay Grosfeld ScholarAmerican Pediatric Surgical Association Jay Grosfeld Scholar GrantAssistant Secretary of Defense for Health AffairsBoston Children's HospitalDepartment of DefenseHardy Hendren Faculty Development Fund at Boston Children's HospitalJunior Translational Investigator ServiceNICHD NIH HHS K99 HD115239NIH HHS K99HD115239Peer Reviewed Medical Research Program #HT9425-23-1-0040Society of University Surgeons Junior FacultySociety of University Surgeons Junior Faculty AwardTranslational Research Program at Boston Children's Hospital
6 · The paper itself

Abstract

Adjuvants are widely used to boost the immune response during vaccination protocols. Our group has previously reported that repeated intraperitoneal administration of alum in mice, known as adjuvant conditioning (AC), creates an immunosuppressive environment that delays allogeneic graft rejection through NLRP3-dependent MDSC expansion. However, little is known about the effects of AC on the reprogramming of peritoneal cavity cells, particularly the different peritoneal macrophage populations, and the impact on the adaptive immune response. We found a population-specific immune response to alum, with small peritoneal macrophages (SPMs) being more prone to inflammasome activation than large peritoneal macrophages (LPMs) in vitro. In vivo, alum exposure led to NLRP3-dependent macrophage disappearance reaction (MDR) of LPMs, which could be explained by aggregate formation and migration to the omentum. AC also induced the reprogramming of resident macrophages and infiltrating monocytes towards a less inflammatory state, making them more vulnerable to bacterial infections, but recruited neutrophils with enhanced killing ability. This suggests that AC may influence both innate and adaptive immunity in distinct ways, reprogramming cells to different profiles, and indicating its potential as an immunosuppressive treatment for autoimmune diseases and transplant rejection.

Indexed as

Adjuvants, ImmunologicAlum CompoundsMacrophages, PeritonealNeutrophilsAnimalsImmunity, InnateInflammasomesMiceMice, Inbred C57BLMice, KnockoutNLR Family, Pyrin Domain-Containing 3 ProteinPhenotypeAdjuvants, ImmunologicAlum Compoundsaluminum sulfateInflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseadjuvant conditioningimmune suppressioninnate immunity

Identifiers

PMID40897376
PMCPMC12726067

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.