Evidence map›Paper›PMID 41604784›Full record

ArticleNuclear medicine and biology

In vitro evaluation of anti-HIV radioimmunoconjugates labeled with astatine-211, thorium-227 and actinium-225.

Anne-Sophie Kuhlmann, Donald K Hamlin, Yawen Li, Xinyi Wang, Lily Li, Chris Orvig, Hans-Peter Kiem, Brenda M Sandmaier, D Scott Wilbur, Seth Pincus and 1 more

Abstract read
In one paragraph

Article in Nuclear medicine and biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Anne-Sophie KuhlmannTranslational Science & Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA. Electronic address: akuhlman@fredhutch.org.
Donald K HamlinDepartment of Radiation Oncology, University of Washington, Seattle, WA, USA.
Yawen LiDepartment of Radiation Oncology, University of Washington, Seattle, WA, USA.
Xinyi WangTranslational Science & Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Lily LiMedicinal Inorganic Chemistry Group, Department of Chemistry, University of British Columbia, Vancouver, BC, Canada.
Chris OrvigMedicinal Inorganic Chemistry Group, Department of Chemistry, University of British Columbia, Vancouver, BC, Canada.
Hans-Peter KiemTranslational Science & Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Department of Medicine, University of Washington, Seattle, WA, USA.
Brenda M SandmaierTranslational Science & Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Department of Medicine, University of Washington, Seattle, WA, USA.
D Scott WilburDepartment of Radiation Oncology, University of Washington, Seattle, WA, USA.
Seth PincusDepartment of Chemistry & Biochemistry, Montana State University, Bozeman, MT, USA.
Robert D HarringtonDepartment of Medicine, University of Washington, Seattle, WA, USA. Electronic address: rdh@uw.edu.

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Cytotoxic immunoconjugates to deplete persistent HIV reservoirsR01AI136758 · NIAID · MONTANA STATE UNIVERSITY - BOZEMAN · PI HARRINGTON, ROBERT D., PINCUS, SETH H. · 2018 to 2022
$3.5M
NCI NIH HHS P30 CA015704NIAID NIH HHS R01 AI136758
6 · The paper itself

Abstract

We conducted an in vitro investigation of the selective cytotoxicity of alpha-emitting radioimmunoconjugates (α-RICs) directed against cells expressing HIV envelope (Env) proteins. It is well known that monoclonal antibody (mAb)-targeted α-emitting radionuclides can effectively kill antigen-expressing cells; however, the expected low-level expression of HIV antigens on latently infected cells poses an obstacle to all anti-HIV immune-based treatments, including α-RICs. This investigation tested the cytotoxicity of the HIV envelope antigen-binding mAbs, PGT126 (binding gp120) and 7B2 (binding gp41), conjugated with labeling chelators that bind the α-emitters astatine-211 (

methodsHigh specific activity (SA) preparations of the α-RICs were made to increase the proportion of mAb conjugates carrying the α-emitting isotope. RIC cytolytic activity was evaluated against a cell line stably expressing the HIV envelope.

results

conclusionsPotential explanations for these differential effects include the longer half-lives of

Indexed as

ActiniumAstatineImmunoconjugatesThoriumAntibodies, MonoclonalHumansIsotope LabelingActiniumActinium-225Antibodies, MonoclonalAstatineAstatine-211ImmunoconjugatesThoriumThorium-227Actinium-225Astatine-211HIVRadioimmunotherapyThorium-227

Identifiers

PMID41604784
PMCPMC13037367

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.