Evidence map›Paper›PMID 25274446›Full record

ArticleRetrovirology2014

Aggregate complexes of HIV-1 induced by multimeric antibodies.

Daniel J Stieh, Deborah F King, Katja Klein, Pinghuang Liu, Xiaoying Shen, Kwan Ki Hwang, Guido Ferrari, David C Montefiori, Barton Haynes, Punnee Pitisuttithum and 9 more

Abstract read
In one paragraph

Article in Retrovirology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Oligomerization-driven avidity correlates with SARS-CoV-2 cellular binding and inhibition.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Neutralization Sensitivity of a Novel HIV-1 CRF01_AE Panel of Infectious Molecular Clones.Journal of acquired immune deficiency syndromes (1999) · 2018
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Antibody-mediated immune exclusion of HIV.Current opinion in HIV and AIDS · 2017
    Review
  17. Review
  18. Review
  19. Article
  20. Article
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

19 authors.

Daniel J StiehCenter for Infection, Department of Cellular and Molecular Medicine, St George's, University of London, London, SW17 0RE, UK. dstieh@northwestern.edu.
Deborah F KingMucosal Infection & Immunity Group, Section of Infectious Diseases, Imperial College London, St Mary's Campus, London, W2 1PG, UK. d.king@imperial.ac.uk.
Katja KleinMucosal Infection & Immunity Group, Section of Infectious Diseases, Imperial College London, St Mary's Campus, London, W2 1PG, UK. k.klein11@imperial.ac.uk.
Pinghuang LiuDuke Human Vaccine Center, Duke University Medical Center, Durham, NC, 27710, USA. ping.liu@duke.edu.
Xiaoying ShenDuke Human Vaccine Center, Duke University Medical Center, Durham, NC, 27710, USA. sxshen@duke.edu.
Kwan Ki HwangDuke Human Vaccine Center, Duke University Medical Center, Durham, NC, 27710, USA. kkhwang@duke.edu.
Guido FerrariDuke Human Vaccine Center, Duke University Medical Center, Durham, NC, 27710, USA. gflmp@duke.edu.
David C MontefioriDuke Human Vaccine Center, Duke University Medical Center, Durham, NC, 27710, USA. id.montefiori@duke.edu.
Barton HaynesDuke Human Vaccine Center, Duke University Medical Center, Durham, NC, 27710, USA. hayne002@mc.duke.edu.
Punnee PitisuttithumFaculty of Tropical Medicine, Mahidol, Thailand. punnee.pit@mahidol.ac.th.
Jaranit KaewkungwalFaculty of Tropical Medicine, Mahidol, Thailand. tmjkk@mahidol.ac.th.
Sorachai NitayaphanArmed Forces Research Institute of Medical Sciences, Bangkok, Thailand. Sorachain@afrims.org.
Supachai Rerks-NgarmMinistry of Public Health, Bangkok, Thailand. supachai@health.moph.go.th.
Nelson L MichaelMilitary HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America. nmichael@hivresearch.org.
Merlin L RobbMilitary HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America. mrobb@hivresearch.org.
Jerome H KimMilitary HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America. jkim@hivresearch.org.
Thomas N DennyDuke Human Vaccine Center, Duke University Medical Center, Durham, NC, 27710, USA. thomas.denny@duke.edu.
Georgia D TomarasDuke Human Vaccine Center, Duke University Medical Center, Durham, NC, 27710, USA. georgia.tomaras@duke.edu.
Robin J ShattockMucosal Infection & Immunity Group, Section of Infectious Diseases, Imperial College London, St Mary's Campus, London, W2 1PG, UK. r.shattock@imperial.ac.uk.

Funding

Viral Sequencing CoreU19AI067854 · NIAID · DUKE UNIVERSITY · PI CRUMP, JOHN ANDREW · 2006 to 2011
$290.5M
Virus biology scientific research support componentUM1AI100645 · NIAID · DUKE UNIVERSITY · PI MCMICHAEL, ANDREW JAMES · 2012 to 2018
$204.7M
NIAID NIH HHS U19 AI067854NIAID NIH HHS U19 AI067854-05NIAID NIH HHS UM1 AI100645NIAID NIH HHS UM1-AI100645-01
6 · The paper itself

Abstract

backgroundAntibody mediated viral aggregation may impede viral transfer across mucosal surfaces by hindering viral movement in mucus, preventing transcytosis, or reducing inter-cellular penetration of epithelia thereby limiting access to susceptible mucosal CD4 T cells and dendritic cells. These functions may work together to provide effective immune exclusion of virus from mucosal tissue; however little is known about the antibody characteristics required to induce HIV aggregation. Such knowledge may be critical to the design of successful immunization strategies to facilitate viral immune exclusion at the mucosal portals of entry.

resultsThe potential of neutralizing and non-neutralizing IgG and IgA monoclonals (mAbs) to induce HIV-1 aggregation was assessed by Dynamic light scattering (DLS). Although neutralizing and non-neutralizing IgG mAbs and polyclonal HIV-Ig efficiently aggregated soluble Env trimers, they were not capable of forming viral aggregates. In contrast, dimeric (but not monomeric) IgA mAbs induced stable viral aggregate populations that could be separated from uncomplexed virions. Epitope specificity influenced both the degree of aggregation and formation of higher order complexes by dIgA. IgA purified from serum of uninfected RV144 vaccine trial responders were able to efficiently opsonize viral particles in the absence of significant aggregation, reflective of monomeric IgA.

conclusionsThese results collectively demonstrate that dIgA is capable of forming stable viral aggregates providing a plausible basis for testing the effectiveness of aggregation as a potential protection mechanism at the mucosal portals of viral entry.

Indexed as

Antibodies, MonoclonalHIV-1HIV AntibodiesHumansImmunoglobulin AImmunoglobulin GAntibodies, MonoclonalHIV AntibodiesImmunoglobulin AImmunoglobulin G

Identifiers

PMID25274446
PMCPMC4193994

What OpenQuestion holds

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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.