Evidence map›Paper›PMID 29762161›Full record

ArticleAIDS (London, England)2018

Anti-HIV IgM protects against mucosal SHIV transmission.

Siqi Gong, Khamis Tomusange, Viraj Kulkarni, Opeyemi S Adeniji, Samir K Lakhashe, Dinesh Hariraju, Amanda Strickland, Elizabeth Plake, Patrice A Frost, Sarah J Ratcliffe and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in AIDS (London, England), 2018. 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
2.4field-weighted citation impact, top 12% 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.

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, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Antibodies for Human Immunodeficiency Virus-1 Cure Strategies.The Journal of infectious diseases · 2021
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Neutralizing antibodies for HIV-1 prevention.Current opinion in HIV and AIDS · 2019
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 1 country.

Siqi GongDepartment of Virology and Immunology, Texas Biomedical Research Institute.
Khamis TomusangeDepartment of Virology and Immunology, Texas Biomedical Research Institute.
Viraj KulkarniDepartment of Virology and Immunology, Texas Biomedical Research Institute.
Opeyemi S AdenijiDepartment of Virology and Immunology, Texas Biomedical Research Institute.
Samir K LakhasheDepartment of Virology and Immunology, Texas Biomedical Research Institute.
Dinesh HarirajuDepartment of Virology and Immunology, Texas Biomedical Research Institute.
Amanda StricklandDepartment of Virology and Immunology, Texas Biomedical Research Institute.
Elizabeth PlakeDepartment of Virology and Immunology, Texas Biomedical Research Institute.
Patrice A FrostSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, Texas.
Sarah J RatcliffeDivision of Biostatistics, Department of Public Health Sciences, University of Virginia, Charlottesville, Virginia.
Liping WangDepartment of Biochemistry and Structural Biology, Center for Biomedical Neuroscience, The University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Eileen M LaferDepartment of Biochemistry and Structural Biology, Center for Biomedical Neuroscience, The University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Ruth M RuprechtDepartment of Virology and Immunology, Texas Biomedical Research Institute.
Texas Biomedical Research Institute · USThe University of Texas Health Science Center at San Antonio · USGTx (United States) · USUniversity of Virginia · US

Funding

The Southwest National Primate Research Center Supplement- Infrastructure improvements of ABSL2 holding areasP51OD011133 · OD · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI Larry S. Schlesinger · 2012 to 2026
$129.7M
TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Robin Jean Leach · 1991 to 2026
$59.1M
Virology and ImmunologyP01AI048240 · NIAID · UNIVERSITY OF WASHINGTON · PI RUPRECHT, RUTH MARGRIT · 2000 to 2020
$46.7M
Functional cure and virus eradication by early HAART plus vaccination with live attenuated rubella virus vectors in macaque infants and neonatesR01AI118586 · NIAID · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI RUPRECHT, RUTH MARGRIT · 2015 to 2018
$5.0M
Humoral Correlates of Protection Against HIVR01AI100703 · NIAID · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI RUPRECHT, RUTH MARGRIT · 2012 to 2016
$4.0M
NCI NIH HHS P30 CA054174NIAID NIH HHS P01 AI048240NIAID NIH HHS R01 AI100703NIAID NIH HHS R01 AI118586NIH HHS P51 OD011133
6 · The paper itself

Abstract

objectiveWorldwide, most new HIV infections occur through mucosal exposure. Immunoglobulin M (IgM) is the first antibody class generated in response to infectious agents; IgM is present in the systemic circulation and in mucosal fluids as secretory IgM. We sought to investigate for the first time the role of IgM in preventing AIDS virus acquisition in vivo.

designRecombinant polymeric monoclonal IgM was generated from the neutralizing monoclonal IgG1 antibody 33C6-IgG1, tested in vitro, and given by passive intrarectal immunization to rhesus macaques 30 min before intrarectal challenge with simian-human immunodeficiency virus (SHIV) that carries an HIV-1 envelope gene.

resultsIn vitro, 33C6-IgM captured virions more efficiently and neutralized the challenge SHIV with a 50% inhibitory molar concentration (IC50) that was 1 log lower than that for 33C6-IgG1. The IgM form also exhibited significantly higher affinity and avidity compared with 33C6-IgG1. After intrarectal administration, 33C6-IgM prevented viremia in four out of six rhesus macaques after high-dose intrarectal SHIV challenge. Five out of six rhesus macaques given 33C6-IgG1 were protected at a five times higher molar concentration compared with the IgM form; all untreated controls became highly viremic. Rhesus macaques passively immunized with 33C6-IgM with breakthrough infection had notably early development of autologous neutralizing antibody responses.

conclusionOur primate model data provide the first proof-of-concept that mucosal IgM can prevent mucosal HIV transmission and have implications for HIV prevention and vaccine development.

Indexed as

Administration, RectalAnimalsAntibodies, MonoclonalDisease Transmission, InfectiousHIV AntibodiesImmunization, PassiveImmunoglobulin MMacaca mulattaRecombinant ProteinsSimian Acquired Immunodeficiency SyndromeTreatment OutcomeAntibodies, MonoclonalHIV AntibodiesImmunoglobulin MRecombinant Proteins

Identifiers

PMID29762161
PMCPMC6380498
OpenAlexW2803410236

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.