Evidence map›Paper›PMID 23401273›Full record

ArticleBlood2013

Immune activation of human brain microvascular endothelial cells inhibits HIV replication in macrophages.

Jieliang Li, Yizhong Wang, Xu Wang, Li Ye, Yu Zhou, Yuri Persidsky, Wenzhe Ho

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

35 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
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  6. Article
  7. Article
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  9. Article
  10. Opioid Use, Gut Dysbiosis, Inflammation, and the Nervous System.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2022
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Neuroinflammation During RNA Viral Infections.Annual review of immunology · 2019
    Review
  20. 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

7 authors at 1 institution in 2 countries.

Jieliang LiAnimal Biosafety Level 3 Laboratory, School of Medicine, Wuhan University, Wuhan, People's Republic of China.
Yizhong Wang
Xu Wang
Li Ye
Yu Zhou
Yuri Persidsky
Wenzhe Ho
Temple University · US

Funding

Drug Abuse, Sustance P and HIVR01DA012815 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI HO, WENZHE · 2000 to 2013
$4.5M
Opioids, HIV/HCV and Host Cell Innate ImmunityR01DA022177 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI HO, WENZHE · 2007 to 2017
$2.9M
Opioids, LPS and HIVR01DA027550 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI HO, WENZHE · 2010 to 2014
$1.4M
NIDA NIH HHS DA012815NIDA NIH HHS DA022177NIDA NIH HHS DA027550NIDA NIH HHS R01 DA012815NIDA NIH HHS R01 DA022177NIDA NIH HHS R01 DA027550
6 · The paper itself

Abstract

There is limited information about the role of blood-brain barrier (BBB) endothelial cells (ECs) in the central nervous system (CNS) and their innate immunity against HIV. We examined whether brain ECs can be immunologically activated to produce antiviral factors that inhibit HIV replication in macrophages. Human brain microvascular ECs expressed functional toll-like receptor 3 (TLR3) that could be activated by polyinosinic-polycytidylic acid (PolyI:C), resulting in the induction of endogenous interferon-β (IFN-β) and IFN-λ. The TLR3 activation of ECs also induced the phosphorylation of interferon regulatory transcription factor 3 (IRF3) and IRF7, the key regulators of IFN signaling pathway. When supernatant (SN) of PolyI:C-activated EC cultures was applied to infected macrophage cultures, HIV replication was significantly suppressed. This SN action of ECs on HIV was mediated through both IFN-β and IFN-λ because antibodies to their receptors could neutralize the SN-mediated anti-HIV effect. The role of IFNs in EC-mediated anti-HIV activity is further supported by the observation that treatment with SN from EC cultures induced the expression of IFN-stimulated genes (ISGs: ISG56, OAS-1, and MxA) in macrophages. These observations indicate that brain microvascular ECs may be a key regulatory bystander, playing a crucial role in the BBB innate immunity against HIV infection.

Indexed as

Active Transport, Cell NucleusBlood-Brain BarrierBlotting, WesternBrainCell NucleusCells, CulturedCulture Media, ConditionedDEAD Box Protein 58DEAD-box RNA HelicasesEndothelial CellsHIV-1HumansInterferon-betaInterferon-gammaInterferon Regulatory Factor-3Interferon Regulatory Factor-7Culture Media, ConditionedDEAD Box Protein 58DEAD-box RNA HelicasesInterferon-betaInterferon-gammaInterferon Regulatory Factor-3Interferon Regulatory Factor-7IRF3 protein, humanIRF7 protein, humanPoly I-CReceptors, ImmunologicRIGI protein, humanTLR3 protein, humanToll-Like Receptor 3

Identifiers

PMID23401273
PMCPMC3624939
OpenAlexW2072881516

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.