Evidence map›Paper›PMID 40259346›Full record

ArticleJournal of neuroinflammation2025

Endothelial -targeted CD39 is protective in a mouse model of global forebrain ischaemia.

Natasha Ting Lee, Ioanna Savvidou, Carly Selan, David K Wright, Robert Brkljaca, Joanne S J Chia, Ilaria Calvello, Daphne D D Craenmehr, Pia Larsson, Volga Tarlac and 7 more

Abstract read
In one paragraph

Article in Journal of neuroinflammation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. NADInternational journal of molecular sciences · 2026
    Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. 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

17 authors.

Natasha Ting Lee *Department of Neuroscience, School of Translational Medicine, Monash University, Melbourne, VIC, 3004, Australia.
Ioanna Savvidou *Australian Centre for Blood Diseases, School of Translational Medicine, Alfred Hospital, Monash University, Melbourne, VIC, 3004, Australia.
Carly SelanAustralian Centre for Blood Diseases, School of Translational Medicine, Alfred Hospital, Monash University, Melbourne, VIC, 3004, Australia.
David K WrightDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, VIC, 3004, Australia.
Robert BrkljacaMonash Biomedical Imaging, Monash University, Clayton, VIC, 3168, Australia.
Joanne S J ChiaAustralian Centre for Blood Diseases, School of Translational Medicine, Alfred Hospital, Monash University, Melbourne, VIC, 3004, Australia.
Ilaria CalvelloAustralian Centre for Blood Diseases, School of Translational Medicine, Alfred Hospital, Monash University, Melbourne, VIC, 3004, Australia.
Daphne D D CraenmehrAustralian Centre for Blood Diseases, School of Translational Medicine, Alfred Hospital, Monash University, Melbourne, VIC, 3004, Australia.
Pia LarssonAustralian Centre for Blood Diseases, School of Translational Medicine, Alfred Hospital, Monash University, Melbourne, VIC, 3004, Australia.
Volga TarlacAustralian Centre for Blood Diseases, School of Translational Medicine, Alfred Hospital, Monash University, Melbourne, VIC, 3004, Australia.
Amy VuongAustralian Centre for Blood Diseases, School of Translational Medicine, Alfred Hospital, Monash University, Melbourne, VIC, 3004, Australia.
Irena CarmichaelMonash Micro Imaging-ARA, Sub-Faculty of Translational Medicine and Public Health, Monash University, 89 Commercial Road, Melbourne, VIC, 3004, Australia.
Xiaowei WangAtherothrombosis and Vascular Biology Laboratory, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
Karlheinz PeterAtherothrombosis and Vascular Biology Laboratory, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
Simon C RobsonCenter for Inflammation Research, Department of Anesthesia, Critical Care & Pain Medicine, Division of Gastroenterology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Harshal H Nandurkar *Australian Centre for Blood Diseases, School of Translational Medicine, Alfred Hospital, Monash University, Melbourne, VIC, 3004, Australia.
Maithili Sashindranath *Australian Centre for Blood Diseases, School of Translational Medicine, Alfred Hospital, Monash University, Melbourne, VIC, 3004, Australia. maithili.sashindranath@monash.edu.

Funding

Bethlehem Griffiths Research Foundation 1708National Health and Medical Research Council APP1141046
6 · The paper itself

Abstract

Global ischemic brain injury occurs after cardiac arrest or prolonged hypotensive episodes following surgery or trauma. It causes significant neurological deficits even after successful re-establishment of blood flow. It is the primary cause of death in 68% of inpatient and 23% of out-of-hospital cardiac arrest cases, but there are currently no treatments. Endothelial activation and dysfunction impairing small vessel blood flow is the cause of brain damage. Purinergic signaling is an endogenous molecular pathway, where CD39 and CD73 catabolize extracellular adenosine triphosphate (eATP) to adenosine. After ischemia, eATP is released, triggering thrombosis and inflammation. In contrast, adenosine is anti-thrombotic, protects against oxidative stress, and suppresses the immune response. Our group developed a bifunctional compound - anti-VCAM-CD39 that targets the dysregulated endothelium and promotes adenosine generation at the infarct site, localising the antithrombotic and anti-inflammatory effects of CD39. We investigated whether anti-VCAM-CD39 could improve outcome in a murine model of global ischaemia caused by dual carotid artery ligation (DCAL). Test drugs anti-VCAM-CD39 and controls were given 3 h after 30 min ischaemia. Assessments at 24 h included neurological function, infarct volume, perfusion, and albumin extravasation to assess blood-brain barrier (BBB) permeability. We showed that there was an overall improvement in neurological deficit in anti-VCAM-CD39-treated mice after DCAL. MRI revealed that these mice had significantly smaller infarcts and reduced apoptotic activity on the side of permanent occlusion, compared to saline treated mice. There was reduced albumin extravasation in treated mice after DCAL, suggesting anti-VCAM-CD39 conferred neuroprotection in the brain through preservation of BBB permeability. In vitro findings confirmed that anti-VCAM-CD39-mediated adenosine production protected against hypoxia-induced endothelial cell death. anti-VCAM-CD39 is a novel therapeutic that can promote neuroprotection, reduce tissue damage and inflammation after hypoxic brain injury in mice. These findings suggest that anti-VCAM-CD39 could be a new avenue of cardiac arrest therapy and could potentially be used in other cerebrovascular diseases where endothelial dysfunction is a constant underlying pathology.

Indexed as

Antigens, CDApyraseBrain IschemiaProsencephalonAnimalsBlood-Brain BarrierDisease Models, AnimalMaleMiceMice, Inbred C57BLAntigens, CDApyraseCD39 antigenCD39Dual carotid artery ligationGlobal hypoxiaIschaemiaVCAM-1

Identifiers

PMID40259346
PMCPMC12013200

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.