Evidence map›Paper›PMID 19933330›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

The integrin alpha4beta7 forms a complex with cell-surface CD4 and defines a T-cell subset that is highly susceptible to infection by HIV-1.

Claudia Cicala, Elena Martinelli, Jonathan P McNally, Diana J Goode, Ravindra Gopaul, Joseph Hiatt, Katija Jelicic, Shyamasundaran Kottilil, Katilyn Macleod, Angeline O'Shea and 11 more

2 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 188 papers.

0numbers the graph read from it
0cells of the map it votes in
188citing papers in PubMed
5.8field-weighted citation impact, top 3% 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.

NCT02788175 phase1completednot on this mapstarted 2016, after this paper: background citation

An Exploratory, Open-Label Study of Vedolizumab (Anti-alpha4beta7 Antibody) in Subjects With HIV Infection Undergoing Analytical Treatment Interruption

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2016 to 2019Enrolled26ConditionsHIVArmsEntyvio (Vedolizumab)
NCT03577782 phase1 / phase2unknown statusnot on this mapstarted 2018, after this paper: background citation

Phase II Clinical Trial to Analyze the Safety and Efficacy of Vedolizumab Combined With Antiretroviral Therapy to Achieve Permanent Virological Remission in HIV-infected Subjects Without Previous Antiretroviral Therapy

TypeinterventionalSponsorHospitales Universitarios Virgen del RocíoRan2018 to 2020Enrolled12ConditionsHIV InfectionsArmsEntyvio (Vedolizumab)
3 · Its place in the literature

Who cites it

188 citing papers in PubMed, 281 citations in OpenAlex.

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  18. Impact ofTropical medicine and infectious disease · 2025
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128 more citing papers are in PubMed but not listed here.

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

21 authors at 3 institutions in 3 countries.

Claudia CicalaLaboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA. ccicala@niaid.nih.gov
Elena Martinelli
Jonathan P McNally
Diana J Goode
Ravindra Gopaul
Joseph Hiatt
Katija Jelicic
Shyamasundaran Kottilil
Katilyn Macleod
Angeline O'Shea
Nikita Patel
Donald Van Ryk
Danlan Wei
Massimiliano Pascuccio
Ling Yi
Lyle McKinnon
Preson Izulla
Joshua Kimani
Rupert Kaul
Anthony S Fauci
James Arthos
University of Nairobi · KEUniversity of Toronto · CANational Institute of Allergy and Infectious Diseases · US

Funding

Role of HIV Envelope Proteins In Viral Replication and HIV PathogenesisZIAAI000887 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI CICALA, CLAUDIA · 2009 to 2025
$15.2M
Interaction of HIV envelope with cell surface receptorsZIAAI000883 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI ARTHOS, JAMES L · 2009 to 2024
$14.0M
Intramural NIH HHS
6 · The paper itself

Abstract

Both activated and resting CD4(+) T cells in mucosal tissues play important roles in the earliest phases of infection after sexual transmission of HIV-1, a process that is inefficient. HIV-1 gp120 binds to integrin alpha(4)beta(7) (alpha(4)beta(7)), the gut mucosal homing receptor. We find that alpha(4)beta(7)(high) CD4(+) T cells are more susceptible to productive infection than are alpha(4)beta(7)(low-neg) CD4(+) T cells in part because this cellular subset is enriched with metabolically active CD4(+) T cells. alpha(4)beta(7)(high) CD4(+) T cells are CCR5(high) and CXCR4(low); on these cells, alpha(4)beta(7) appears in a complex with CD4. The specific affinity of gp120 for alpha(4)beta(7) provides a mechanism for HIV-1 to target activated cells that are critical for efficient virus propagation and dissemination following sexual transmission.

Indexed as

Antibodies, MonoclonalCD4 AntigensCD4-Positive T-LymphocytesCell MembraneFemaleGenitalia, FemaleHIV-1HIV InfectionsHumansImmunoprecipitationIntegrinsIntestinal MucosaLymphocyte ActivationReceptors, CCR5T-Lymphocyte SubsetsVirus ReplicationAntibodies, MonoclonalCD4 Antigensintegrin alpha4beta7IntegrinsReceptors, CCR5

Identifiers

PMID19933330
PMCPMC2780317
OpenAlexW2159593123

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.