Evidence map›Paper›PMID 24191027›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

MCPIP1 restricts HIV infection and is rapidly degraded in activated CD4+ T cells.

Shufeng Liu, Chao Qiu, Ruidong Miao, Jianhua Zhou, Aram Lee, Baoming Liu, Sandra N Lester, Weihui Fu, Lingyan Zhu, Linxia Zhang and 5 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 2 pooled it
–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

49 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. High rates of Treponema pallidum, Neisseria gonorrhoeae, Chlamydia trachomatis, or Trichomonas vaginalis co-infection in people with HIV: a systematic review and meta-analysis.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
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  11. Risk factors for pneumonia among children with coinfection of influenza A virus and Mycoplasma pneumoniae.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2024
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  16. MALT1 substrate cleavage: what is it good for?Frontiers in immunology · 2024
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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

15 authors.

Shufeng LiuDepartment of Infectious Diseases and Microbiology, University of Pittsburgh, Pittsburgh, PA 15261.
Chao Qiu
Ruidong Miao
Jianhua Zhou
Aram Lee
Baoming Liu
Sandra N Lester
Weihui Fu
Lingyan Zhu
Linxia Zhang
Jianqing Xu
Daping Fan
Kui Li
Mingui Fu
Tianyi Wang

Funding

Tight Junction: Gate to HCV Tropism, Therapeutics and PathogenesisR01DK088787 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STEIN, PAUL L · 2010 to 2019
$4.2M
Role of TLR3 Signaling in Control of HCVR01AI069285 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI LI, KUI · 2007 to 2016
$2.5M
Training Grant in Bacterial PathogenesisT32AI078906 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI BYRNE, GERALD IRWIN · 2009 to 2013
$339k
Role of TLR3 Signaling in Control of HCVR56AI069285 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI LI, KUI · 2012 to 2012
$300k
NIAID NIH HHS AI069285NIAID NIH HHS AI078906NIAID NIH HHS R01 AI069285NIAID NIH HHS R56 AI069285NIAID NIH HHS T32 AI078906NIDDK NIH HHS R01 DK088787NIDDK NIH HHS R01DK088787
6 · The paper itself

Abstract

HIV-1 primarily infects activated CD4+ T cells and macrophages. Quiescent CD4+ T cells, however, possess cellular factors that limit HIV-1 infection at different postentry steps of the viral life cycle. Here, we show that the previously reported immune regulator monocyte chemotactic protein-induced protein 1 (MCPIP1) restricts HIV-1 production in CD4+ T cells. While the ectopic expression of MCPIP1 in cell lines abolished the production of HIV-1, silencing of MCPIP1 enhanced HIV-1 production. Subsequent analysis indicated that MCPIP1 imposes its restriction by decreasing the steady levels of viral mRNA species through its RNase domain. Remarkably, common T-cell stimuli induced the rapid degradation of MCPIP1 in both T-cell lines and quiescent human CD4+ T cells. Lastly, blocking the proteosomal degradation of MCPIP1 by MG132 abrogated HIV-1 production in phorbol 12-myristate 13-acetate/ionomycin-stimulated human CD4+ T cells isolated from healthy donors. Overall, MCPIP1 poses a potent barrier against HIV-1 infection at a posttranscriptional stage. Although the observed HIV restriction conferred by MCPIP1 does not seem to be overcome by any viral protein, it is removed during cellular stimulation. These findings provide insights into the mechanisms of cellular activation-mediated HIV-1 production in CD4+ T cells.

Indexed as

Blotting, NorthernCD4-Positive T-LymphocytesHEK293 CellsHIV InfectionsHumansImmunoblottingLeupeptinsLymphocyte ActivationProteolysisReal-Time Polymerase Chain ReactionRibonucleasesRNA, Small InterferingTranscription Factorsbenzyloxycarbonylleucyl-leucyl-leucine aldehydeLeupeptinsRibonucleasesRNA, Small InterferingTranscription FactorsZC3H12A protein, humanantiviral immunityrestriction factor

Identifiers

PMID24191027
PMCPMC3839757

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.