Evidence map›Paper›PMID 28341672›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

Activation of Myeloid TLR4 Mediates T Lymphocyte Polarization after Traumatic Brain Injury.

Molly Braun, Kumar Vaibhav, Nancy Saad, Sumbul Fatima, Darrell W Brann, John R Vender, Lei P Wang, Md Nasrul Hoda, Babak Baban, Krishnan M Dhandapani

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.4field-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

44 citing papers in PubMed, 77 citations in OpenAlex.

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  11. Regulatory T lymphocytes in traumatic brain injury.Neurochemistry international · 2024
    Review
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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

10 authors at 3 institutions in 1 country.

Molly BraunDepartment of Neurosurgery, Medical College of Georgia, Augusta University, Augusta, GA 30912.
Kumar VaibhavDepartment of Neurosurgery, Medical College of Georgia, Augusta University, Augusta, GA 30912.
Nancy SaadDepartment of Oral Biology, Dental College of Georgia, Augusta University, Augusta, GA 30912.
Sumbul FatimaDepartment of Medical Laboratory, Imaging, and Radiological Sciences, College of Allied Health Sciences, Augusta University, Augusta, GA 30912.
Darrell W BrannDepartment of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, Augusta, GA 30912.
John R VenderDepartment of Neurosurgery, Medical College of Georgia, Augusta University, Augusta, GA 30912.
Lei P WangDepartment of Psychiatry, Medical College of Georgia, Augusta University, Augusta, GA 30912; and.
Md Nasrul HodaDepartment of Medical Laboratory, Imaging, and Radiological Sciences, College of Allied Health Sciences, Augusta University, Augusta, GA 30912.
Babak BabanDepartment of Oral Biology, Dental College of Georgia, Augusta University, Augusta, GA 30912.
Krishnan M DhandapaniDepartment of Neurosurgery, Medical College of Georgia, Augusta University, Augusta, GA 30912; kdhandapani@augusta.edu.
Augusta University · USAugusta University Health · USCharlie Norwood VA Medical Center · US

Funding

HMGB1 and Traumatic Brain InjuryR01NS065172 · NINDS · AUGUSTA UNIVERSITY · PI DHANDAPANI, KRISHNAN M. · 2009 to 2013
$1.6M
Immune Mechanisms of Protection by Remote Limb Ischemic Conditioning after Intracerebral HemorrhageR21NS095154 · NINDS · AUGUSTA UNIVERSITY · PI DHANDAPANI, KRISHNAN M. · 2015 to 2016
$418k
NLRP3 inflammasome and TBIR03NS084228 · NINDS · AUGUSTA UNIVERSITY · PI DHANDAPANI, KRISHNAN M. · 2013 to 2014
$149k
Role of NADPH Oxidase in TBI PathologyI01BX001117 · VA · CHARLIE NORWOOD VA MEDICAL CENTER · PI BRANN, DARRELL W · 2014 to 2017
–
BLRD VA I01 BX001117NINDS NIH HHS R01 NS065172NINDS NIH HHS R03 NS084228NINDS NIH HHS R21 NS095154
6 · The paper itself

Abstract

Traumatic brain injury (TBI) is a major public health issue, producing significant patient mortality and poor long-term outcomes. Increasing evidence suggests an important, yet poorly defined, role for the immune system in the development of secondary neurologic injury over the days and weeks following a TBI. In this study, we tested the hypothesis that peripheral macrophage infiltration initiates long-lasting adaptive immune responses after TBI. Using a murine controlled cortical impact model, we used adoptive transfer, transgenic, and bone marrow chimera approaches to show increased infiltration and proinflammatory (classically activated [M1]) polarization of macrophages for up to 3 wk post-TBI. Monocytes purified from the injured brain stimulated the proliferation of naive T lymphocytes, enhanced the polarization of T effector cells (T

Indexed as

Adaptive ImmunityAdoptive TransferAnimalsBrain Injuries, TraumaticCell DifferentiationCell MovementCell ProliferationCells, CulturedCoculture TechniquesDisease Models, AnimalHumansMacrophagesMaleMiceMice, Inbred C3HMice, Inbred C57BLTlr4 protein, mouseToll-Like Receptor 4

Identifiers

PMID28341672
PMCPMC5417078
OpenAlexW2598138822

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.