Evidence map›Paper›PMID 36070344›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Monocytes maintain central nervous system homeostasis following helminth-induced inflammation.

Jianya Peng, Chandler B Sy, John J Ponessa, Alexander D Lemenze, Christina M Hernandez, Juan M Inclan-Rico, Arman Sawhney, Hannah G Federman, Krupa Chavan, Vanessa Espinosa and 3 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 34% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
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

13 authors at 1 institution in 1 country.

Jianya PengCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.ORCID 0000-0002-2617-3626
Chandler B SyCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.
John J PonessaCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.ORCID 0000-0002-0245-7667
Alexander D LemenzeDepartment of Pathology, Immunology, and Laboratory Medicine, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.
Christina M HernandezCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.ORCID 0000-0001-5788-6138
Juan M Inclan-RicoCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.ORCID 0000-0003-1134-9139
Arman SawhneyCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.ORCID 0000-0002-4039-9082
Hannah G FedermanCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.
Krupa ChavanCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.
Vanessa EspinosaCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.ORCID 0000-0003-4808-3557
Sergei V KotenkoCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.
Amariliz RiveraCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.
Mark C SiracusaCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.ORCID 0000-0003-3499-5408
Rutgers, The State University of New Jersey · US

Funding

Neuropeptide-mediated regulation of antihelminth immunityR01AI151599 · NIAID · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI ARTIS, DAVID, SIRACUSA, MARK CHRISTOPHER · 2020 to 2024
$3.2M
Trained immunity and the regulation of anti-fungal defenseR01AI169769 · NIAID · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI Amariliz Rivera, Chaoyang Xue · 2022 to 2026
$3.1M
Protective and pathologic functions of macrophages induced by helminthsR01AI131634 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI GAUSE, WILLIAM CLARK, SIRACUSA, MARK CHRISTOPHER · 2018 to 2022
$2.6M
Innate Immune regulation of helminth-induced inflammationR01AI123224 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI SIRACUSA, MARK CHRISTOPHER · 2016 to 2020
$2.0M
Program in Infection, Immunity and InflammationT32AI125185 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI SALGAME, PADMINI · 2016 to 2020
$747k
New innovations: advancing mast cell biologyR21AI171064 · NIAID · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI SIRACUSA, MARK CHRISTOPHER · 2022 to 2023
$432k
NIAID NIH HHS R01 AI123224NIAID NIH HHS R01 AI131634NIAID NIH HHS R01 AI151599NIAID NIH HHS R01 AI169769NIAID NIH HHS R21 AI171064NIAID NIH HHS T32 AI125185
6 · The paper itself

Abstract

Neuroimmune interactions are crucial for regulating immunity and inflammation. Recent studies have revealed that the central nervous system (CNS) senses peripheral inflammation and responds by releasing molecules that limit immune cell activation, thereby promoting tolerance and tissue integrity. However, the extent to which this is a bidirectional process, and whether peripheral immune cells also promote tolerance mechanisms in the CNS remains poorly defined. Here we report that helminth-induced type 2 inflammation promotes monocyte responses in the brain that are required to inhibit excessive microglial activation and host death. Mechanistically, infection-induced monocytes express YM1 that is sufficient to inhibit tumor necrosis factor production from activated microglia. Importantly, neuroprotective monocytes persist in the brain, and infected mice are protected from subsequent lipopolysaccharide-induced neuroinflammation months after infection-induced inflammation has resolved. These studies demonstrate that infiltrating monocytes promote CNS homeostasis in response to inflammation in the periphery and demonstrate that a peripheral infection can alter the immunologic landscape of the host brain.

Indexed as

BrainEncephalitisHomeostasisMonocytesNeuroimmunomodulationTrichinella spiralisTrichinellosisAnimalsbeta-N-AcetylhexosaminidasesLectinsMiceMicrogliabeta-N-AcetylhexosaminidasesChil3 protein, mouseLectinshelminthinnate immune cellsmonocyteneuroimmune cross-talk

Identifiers

PMID36070344
PMCPMC9478671
OpenAlexW4294884745

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.