Evidence map›Paper›PMID 26980009›Full record

ArticleNeurochemical research2016

Blocking B7-1/CD28 Pathway Diminished Long-Range Brain Damage by Regulating the Immune and Inflammatory Responses in a Mouse Model of Intracerebral Hemorrhage.

Lu Ma, Xi Shen, Yuan Gao, Qiong Wu, Mengmeng Ji, Chengliang Luo, Mingyang Zhang, Tao Wang, Xiping Chen, Luyang Tao

Abstract read
PubMed Publisher
In one paragraph

Article in Neurochemical research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. Review
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  6. 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 1 institution in 1 country.

Lu MaDepartment of Forensic Medicine, Medical School of Soochow University, No. 178, Ganjiang East Road, Soochow, 215123, China.
Xi ShenDepartment of Forensic Medicine, Medical School of Soochow University, No. 178, Ganjiang East Road, Soochow, 215123, China.
Yuan GaoDepartment of Forensic Medicine, Medical School of Soochow University, No. 178, Ganjiang East Road, Soochow, 215123, China.
Qiong WuDepartment of Forensic Medicine, Medical School of Soochow University, No. 178, Ganjiang East Road, Soochow, 215123, China.
Mengmeng JiDepartment of Forensic Medicine, Medical School of Soochow University, No. 178, Ganjiang East Road, Soochow, 215123, China.
Chengliang LuoDepartment of Forensic Medicine, Medical School of Soochow University, No. 178, Ganjiang East Road, Soochow, 215123, China.
Mingyang ZhangDepartment of Forensic Medicine, Medical School of Soochow University, No. 178, Ganjiang East Road, Soochow, 215123, China.
Tao WangDepartment of Forensic Medicine, Medical School of Soochow University, No. 178, Ganjiang East Road, Soochow, 215123, China.
Xiping ChenDepartment of Forensic Medicine, Medical School of Soochow University, No. 178, Ganjiang East Road, Soochow, 215123, China.
Luyang TaoDepartment of Forensic Medicine, Medical School of Soochow University, No. 178, Ganjiang East Road, Soochow, 215123, China. luyang.tao@163.com.
Soochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute brain injuries can activate bidirectional crosstalk between the injured brain and the immune system. The immune system, particularly T lymphocytes and cytokines, has been implicated in the progression of brain injury after intracerebral hemorrhage (ICH). Co-stimulatory molecules B7-1 (CD80)/B7-2 (CD86) binding cognate receptor provides a secondary signaling to T cell activation. The aim of our study was to explore the effects of anti-B7-1 antibody on the development and prognosis of cerebral hemorrhage and to investigate the possible underlying mechanism. Mice were inner canthus veniplex administered with anti-B7-1 antibody at 10 min and 24 h after ICH and sacrificed on the third day after ICH. Immune function was assessed via splenocyte proliferation assay and organism index, respectively. IFN-γ and IL-4 were detected by enzyme-linked immuno sorbent assay. The cerebral edema was evaluated via brain water content. The levels of autophagy and apoptosis related proteins were measured by western blotting analysis. In addition, functional outcome was studied with pole-climbing test and morris water maze. The mice were weighed on 0, 1, 3, 14 and 21 days after ICH. The treatment with anti-B7-1 antibody significantly lowered immune function, and reduced the latency of water maze on 18 and 20 days, the ratio of IFN-γ/IL-4 as well as body weight on day 3 after cerebral hemorrhage. Our study suggests that in the cerebral hemorrhage mice brain anti-B7-1 antibody may reduce long-range brain damage by reversing immune imbalance.

Indexed as

Disease Models, AnimalAnimalsAntibodies, Anti-IdiotypicB7-1 AntigenBrain InjuriesCD28 AntigensCells, CulturedCerebral HemorrhageImmunity, CellularLymphocyte ActivationMaleMiceMice, Inbred ICRSignal TransductionAntibodies, Anti-IdiotypicB7-1 AntigenCD28 AntigensAnti-B7-1 antibodyBehavioristicsCytokinesImmuneIntracerebral hemorrhage

Identifiers

PMID26980009
OpenAlexW2300100075

What OpenQuestion holds

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Registered trials

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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.