Evidence map›Paper›PMID 23908485›Full record

ArticleThe Journal of infectious diseases2013

Postintegration HIV-1 infection of cervical epithelial cells mediates contact-dependent productive infection of T cells.

Amanda M Micsenyi, Chati Zony, Raymond A Alvarez, Natasha D Durham, Benjamin K Chen, Mary E Klotman

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Vaginal Epithelium Transiently Harbours HIV-1 Facilitating Transmission.Frontiers in cellular and infection microbiology · 2021
    Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Interactions between HIV-1 and mucosal cells in the female reproductive tract.American journal of reproductive immunology (New York, N.Y. : 1989) · 2014
    Review
  18. Mucosal immunity in the female genital tract, HIV/AIDS.BioMed research international · 2014
    Review
  19. Article
  20. 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.

Amanda M MicsenyiDepartment of Medicine and Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York.
Chati Zony
Raymond A Alvarez
Natasha D Durham
Benjamin K Chen
Mary E Klotman

Funding

Imaging Virological Synapses During Parenteral HIV TransmissionDP1DA028866 · NIDA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHEN, BENJAMIN K · 2009 to 2013
$4.1M
HIV Integrase as a Target for Topical MIcrobicide DevelopmentR21AI079776 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KLOTMAN, MARY E. · 2008 to 2009
$496k
NIAID NIH HHS R21 AI079776NIAID NIH HHS R21 AI79776-01NIDA NIH HHS DA028866NIDA NIH HHS DP1 DA028866
6 · The paper itself

Abstract

The female genital epithelium plays a protective role against invading pathogens; however, sexual transmission of human immunodeficiency virus type 1 (HIV-1) still occurs in healthy women. To model virus-cell interactions in this barrier during sexual transmission, we studied the uptake and infection of ectocervical and endocervical cell lines with cell-free fluorescent protein-expressing recombinant HIV-1 carrying primary transmitted/founder envelope genes. We observed that a subset of both the ectocervical and endocervical epithelial cells become productively infected with cell-free HIV-1 in a CD4-independent manner. In addition, the ability of the semen-derived enhancer of virus infection (SEVI) to enhance virus-epithelial cell interactions was studied. This infection is increased approximately 2-5 fold when inoculation occurs in the presence of SEVI fibrils. Once infected, the epithelial cells are capable of transmitting the virus to target CD4 T cells in coculture in a contact-dependent manner that uses conventional CD4- and coreceptor-dependent entry. The infection of target CD4 T cells only occurs when de novo HIV-1 is produced within the epithelial cells. These findings suggest that a subset of cervical epithelial cells may be actively involved in establishing a systemic HIV infection and should be a target when designing prevention strategies to protect against HIV-1 sexual transmission.

Indexed as

CD4-Positive T-LymphocytesCell LineCervix UteriEpithelial CellsFemaleGene Expression Regulation, ViralHIV-1HIV InfectionsHost-Pathogen InteractionsHumansRNA, ViralVirus InternalizationRNA, Viralcervical epithelium infectioncocultureSEVItransmitted and founder HIV envelope

Identifiers

PMID23908485
PMCPMC3814833

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.