Evidence map›Paper›PMID 32373131›Full record

ArticleFrontiers in immunology2020

Redirection of Cord Blood T Cells and Natural Killer Cells for Elimination of Autologous HIV-1-Infected Target Cells Using Bispecific DART® Molecules.

Justin Pollara, R Whitney Edwards, Shalini Jha, Chia-Ying Kao Lam, Liqin Liu, Gundo Diedrich, Jeffrey L Nordstrom, Tori Huffman, Joy A Pickeral, Thomas N Denny and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Engaging innate immunity in HIV-1 cure strategies.Nature reviews. Immunology · 2022
    Review
  10. Article
  11. 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

12 authors at 2 institutions in 1 country.

Justin PollaraDepartment of Surgery, Duke University School of Medicine, Durham, NC, United States.
R Whitney EdwardsHuman Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Shalini JhaDepartment of Surgery, Duke University School of Medicine, Durham, NC, United States.
Chia-Ying Kao LamMacrogenics, Inc., Rockville, MD, United States.
Liqin LiuMacrogenics, Inc., Rockville, MD, United States.
Gundo DiedrichMacrogenics, Inc., Rockville, MD, United States.
Jeffrey L NordstromMacrogenics, Inc., Rockville, MD, United States.
Tori HuffmanDepartment of Surgery, Duke University School of Medicine, Durham, NC, United States.
Joy A PickeralDepartment of Surgery, Duke University School of Medicine, Durham, NC, United States.
Thomas N DennyHuman Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Sallie R PermarHuman Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Guido FerrariDepartment of Surgery, Duke University School of Medicine, Durham, NC, United States.
Duke University · USMacroGenics (United States) · US

Funding

Social and Behavioral Sciences CoreP30AI064518 · NIAID · DUKE UNIVERSITY · PI Nwora Lance Okeke · 2005 to 2026
$50.5M
Collaboratory of AIDS Researchers for Eradication (CARE)UM1AI126619 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MARGOLIS, DAVID M. · 2016 to 2020
$23.2M
Combined Hepatitis B and HIV-1 envelope vaccination to augment T cell help via linked recognition of unrelated antigensK01OD024877 · OD · DUKE UNIVERSITY · PI POLLARA, JUSTIN JOSEPH · 2017 to 2019
$1.0M
Dual-Affinity Re-Targeting Proteins for Cure of Newborn Infant HIV-1 InfectionR21AI127022 · NIAID · DUKE UNIVERSITY · PI POLLARA, JUSTIN JOSEPH · 2016 to 2017
$437k
NIAID NIH HHS HHSN272201000045CNIAID NIH HHS HHSN272201500032CNIAID NIH HHS HHSN272201700061CNIAID NIH HHS P30 AI064518NIAID NIH HHS R21 AI127022NIAID NIH HHS UM1 AI126619NIH HHS K01 OD024877
6 · The paper itself

Abstract

Mother-to-child transmission of HIV-1 remains a major global health challenge. Currently, HIV-1-infected infants require strict lifelong adherence to antiretroviral therapy to prevent replication of virus from reservoirs of infected cells, and to halt progression of disease. There is a critical need for immune interventions that can be deployed shortly after infection to eliminate HIV-1-infected cells in order to promote long-term remission of viremia, or to potentially cure pediatric HIV-1-infection. Bispecific HIV × CD3 DART® molecules able to co-engage the HIV-1 envelope protein on the surface of infected cells and CD3 on cytolytic T cells have been previously shown to eliminate HIV-1 infected cells

Indexed as

AdultAntibodies, BispecificAntibody-Dependent Cell CytotoxicityBlood DonorsCD4-Positive T-LymphocytesCells, CulturedFemaleFetal BloodHIV-1HIV AntibodiesHIV InfectionsHumansImmunization, PassiveInfectious Disease Transmission, VerticalInterleukin-15Killer Cells, NaturalAntibodies, BispecificHIV AntibodiesIL15 protein, humanInterleukin-15Recombinant Proteinsbispecific DART moleculescytotoxic T cellsnatural killer cellspediatric HIV-1redirected cytotoxicityumbilical cord blood

Identifiers

PMID32373131
PMCPMC7186435
OpenAlexW3020363824

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.