Evidence map›Paper›PMID 39283123›Full record

ArticleJournal of virology2024

Conjugation of anti-HIV gp41 monoclonal antibody to a drug capable of targeting resting lymphocytes produces an effective cytotoxic anti-HIV immunoconjugate.

Seth H Pincus, Frances M Cole, Kelli Ober, Monika Tokmina-Lukaszewska, Tamera Marcotte, Ernest W Kovacs, Tong Zhu, Alisher Khasanov, Valérie Copié, Tami Peters

Abstract read
In one paragraph

Article in Journal of virology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

10 authors.

Seth H PincusDepartment of Chemistry and Biochemistry, Montana State University, Bozeman, Montana, USA.ORCID 0000-0003-1622-4386
Frances M ColeDepartment of Chemistry and Biochemistry, Montana State University, Bozeman, Montana, USA.
Kelli OberDepartment of Chemistry and Biochemistry, Montana State University, Bozeman, Montana, USA.
Monika Tokmina-LukaszewskaDepartment of Chemistry and Biochemistry, Montana State University, Bozeman, Montana, USA.
Tamera MarcotteAnimal Resource Center, Montana State University, Bozeman, Montana, USA.
Ernest W KovacsLevena Biopharma, San Diego, California, USA.
Tong ZhuLevena Biopharma, San Diego, California, USA.
Alisher KhasanovLevena Biopharma, San Diego, California, USA.
Valérie CopiéDepartment of Chemistry and Biochemistry, Montana State University, Bozeman, Montana, USA.
Tami PetersDepartment of Chemistry and Biochemistry, Montana State University, Bozeman, Montana, USA.

Funding

Research Core (Developmental Research Project Program)P20GM103474 · NIGMS · MONTANA STATE UNIVERSITY - BOZEMAN · PI Ann Therese Bertagnolli · 2012 to 2026
$60.0M
Cytotoxic immunoconjugates to deplete persistent HIV reservoirsR01AI136758 · NIAID · MONTANA STATE UNIVERSITY - BOZEMAN · PI HARRINGTON, ROBERT D., PINCUS, SETH H. · 2018 to 2022
$3.5M
Ultra Performance Liquid Chromatography Tandem Mass Spectrometer for MetabolomicsS10OD028650 · OD · MONTANA STATE UNIVERSITY - BOZEMAN · PI BOTHNER, BRIAN P · 2020 to 2020
$599k
HHS | National Institutes of Health (NIH) P20GM103474,S10OD28650HHS | National Institutes of Health (NIH) R01AI136758M.J. Murdock Charitable Trust (MJMCT)NIAID NIH HHS R01 AI136758NIGMS NIH HHS P20 GM103474NIH HHS S10 OD028650
6 · The paper itself

Abstract

HIV-infected cells persisting in the face of suppressive antiretroviral therapy are the barrier to curing infection. Cytotoxic immunoconjugates targeted to HIV antigens on the cell surface may clear these cells. We showed efficacy in mouse and macaque models using immunotoxins, but immunogenicity blunted the effect. As an alternative, we propose antibody drug conjugates (ADCs), as used in cancer immunotherapy. In cancer, the target is a dividing cell, whereas it may not be in HIV. We screened cytotoxic drugs on human primary cells and cell lines. An anthracycline derivative, PNU-159682 (PNU), was highly cytotoxic to both proliferating and resting cells. Human anti-gp41 mAb 7B2 was conjugated to ricin A chain or PNU. The conjugates were tested

Indexed as

Antibodies, MonoclonalHIV Envelope Protein gp41HIV InfectionsImmunoconjugatesAnimalsAnti-HIV AgentsFemaleHIV-1HIV AntibodiesHumansImmunotoxinsLymphocytesMiceRicinAntibodies, MonoclonalAnti-HIV AgentsHIV AntibodiesHIV Envelope Protein gp41ImmunoconjugatesImmunotoxinsRicinantibody drug conjugateHIV persistent reservoirimmunoconjugateimmunotoxin

Identifiers

PMID39283123
PMCPMC11494876

What OpenQuestion holds

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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.