Evidence map›Paper›PMID 41932956›Full record

ArticleNature communications2026

ZFP36L2 is an interferon β -induced inhibitor that restricts the nuclear export of HIV-1 transcripts.

Hailin Pang, Hualu Cui, Xiaowan Yin, Zengwen Yang, Hong Shang, Guoxin Liang

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Hailin Pang *State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Health Commission Key Laboratory of AIDS Prevention and Treatment, The First Hospital of China Medical University, Shenyang, China.ORCID http://orcid.org/0000-0003-2828-0510
Hualu Cui *State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Health Commission Key Laboratory of AIDS Prevention and Treatment, The First Hospital of China Medical University, Shenyang, China.
Xiaowan YinState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Health Commission Key Laboratory of AIDS Prevention and Treatment, The First Hospital of China Medical University, Shenyang, China.
Zengwen YangState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Health Commission Key Laboratory of AIDS Prevention and Treatment, The First Hospital of China Medical University, Shenyang, China.
Hong ShangState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Health Commission Key Laboratory of AIDS Prevention and Treatment, The First Hospital of China Medical University, Shenyang, China. hshang@cmu.edu.cn.ORCID http://orcid.org/0000-0001-5333-8943
Guoxin LiangState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Health Commission Key Laboratory of AIDS Prevention and Treatment, The First Hospital of China Medical University, Shenyang, China. gxliang@cmu.edu.cn.ORCID http://orcid.org/0000-0003-1789-9094

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type I interferons restrict HIV-1 replication by inducing antiviral genes, but the full spectrum of their effectors remains incompletely defined. Here we identify ZFP36L2, a nuclear RNA-binding protein, as an IFN-β-induced inhibitor of HIV-1 infection. Silencing of ZFP36L2 impairs IFN-β-mediated HIV-1 inhibition, whereas overexpression of ZFP36L2 suppresses viral replication. Notably, reconstitution of ZFP36L2 in CD4⁺ T cells from HIV-1-infected individuals reduces viral spread ex vivo, and ZFP36L2 transcript levels inversely correlate with plasma viral loads in vivo. Mechanistically, ZFP36L2 binds to the HIV-1 Rev protein and inhibits the nuclear export of Rev response element-containing viral transcripts, thereby blocking downstream viral protein expression. A Rev mutant lacking amino acids 109-116 fails to bind ZFP36L2 and exhibits resistance to ZFP36L2-mediated inhibition, underscoring the functional significance of this interaction. These findings establish ZFP36L2 as an IFN-β-induced antiviral factor that suppresses HIV-1 replication through Rev-dependent inhibition of viral RNA export.

Indexed as

HIV-1HIV InfectionsInterferon-betaRNA-Binding ProteinsTristetraprolinActive Transport, Cell NucleusCD4-Positive T-LymphocytesCell NucleusHEK293 CellsHumansProtein Bindingrev Gene Products, Human Immunodeficiency VirusRNA, ViralVirus ReplicationInterferon-betarev Gene Products, Human Immunodeficiency Virusrev protein, Human Immunodeficiency Virus-1RNA-Binding ProteinsRNA, ViralTristetraprolin

Identifiers

PMID41932956
PMCPMC13219615

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.