Evidence map›Paper›PMID 30069489›Full record

ArticleJournal of immunology research2018

The Solute Carrier Transporter SLC15A3 Participates in Antiviral Innate Immune Responses against Herpes Simplex Virus-1.

Longzhen He, Baocheng Wang, Yuanyuan Li, Leqing Zhu, Peiling Li, Feiyan Zou, Lianghua Bin

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

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  19. Peroxisomes in Immune Response and Inflammation.International journal of molecular sciences · 2019
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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

7 authors at 1 institution in 2 countries.

Longzhen HeThe First Affiliated Hospital, Biomedical Translational Research Institute, The International Immunology Center and The Key Laboratory of Antibody Engineering of Guangdong Province, Jinan University, Guangzhou, Guangdong Province, China.
Baocheng WangThe First Affiliated Hospital, Biomedical Translational Research Institute, The International Immunology Center and The Key Laboratory of Antibody Engineering of Guangdong Province, Jinan University, Guangzhou, Guangdong Province, China.
Yuanyuan LiThe First Affiliated Hospital, Biomedical Translational Research Institute, The International Immunology Center and The Key Laboratory of Antibody Engineering of Guangdong Province, Jinan University, Guangzhou, Guangdong Province, China.
Leqing ZhuThe First Affiliated Hospital, Biomedical Translational Research Institute, The International Immunology Center and The Key Laboratory of Antibody Engineering of Guangdong Province, Jinan University, Guangzhou, Guangdong Province, China.
Peiling LiThe First Affiliated Hospital, Biomedical Translational Research Institute, The International Immunology Center and The Key Laboratory of Antibody Engineering of Guangdong Province, Jinan University, Guangzhou, Guangdong Province, China.
Feiyan ZouDepartment of Developmental and Regenerative Biology, College of Life Science and Technology, Jinan University, Guangzhou, Guangdong Province, China.
Lianghua BinThe First Affiliated Hospital, Biomedical Translational Research Institute, The International Immunology Center and The Key Laboratory of Antibody Engineering of Guangdong Province, Jinan University, Guangzhou, Guangdong Province, China.ORCID 0000-0002-3786-0106
Jinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The innate immune response is the first line defense against viral infections. Novel genes involved in this system are continuing to emerge. SLC15A3, a proton-coupled histidine and di-tripeptide transporter that was previously found in lysosomes, has been reported to inhibit chikungunya viral replication in host cells. In this study, we found that SLC15A3 was significantly induced by DNA virus herpes simplex virus-1(HSV-1) in monocytes from human peripheral blood mononuclear cells. Aside from monocytes, it can also be induced by HSV-1 in 293T, HeLa cells, and HaCaT cells. Overexpression of SLC15A3 in 293T cells inhibits HSV-1 replication and enhances type I and type III interferon (IFN) responses, while silencing SLC15A3 leads to enhanced HSV-1 replication with reduced IFN production. Moreover, we found that SLC15A3 interacted with MAVS and STING and potentiated MAVS- and STING-mediated IFN production. These results demonstrate that SLC15A3 participates in anti-HSV-1 innate immune responses by regulating MAVS- and STING-mediated signaling pathways.

Indexed as

Adaptor Proteins, Signal TransducingHerpes SimplexHerpesvirus 1, HumanHumansImmunity, InnateMembrane ProteinsMembrane Transport ProteinsSignal TransductionSTING ProteinAdaptor Proteins, Signal TransducingMAVS protein, humanMembrane ProteinsMembrane Transport ProteinsSLC15A3 protein, humanSTING1 protein, humanSTING Protein

Identifiers

PMID30069489
PMCPMC6057324
OpenAlexW2810892887

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.