Evidence map›Paper›PMID 33005704›Full record

ArticleMolecular therapy. Methods & clinical development2020

Engineered Antigen-Specific T Cells Secreting Broadly Neutralizing Antibodies: Combining Innate and Adaptive Immune Response against HIV.

Allison B Powell, Yanqin Ren, Maria Korom, Devin Saunders, Patrick J Hanley, Harris Goldstein, Douglas F Nixon, Catherine M Bollard, Rebecca M Lynch, R Brad Jones and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Methods & clinical development, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
  2. Article
  3. Engineering of CD8mBio · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. [Immunological Causes of Oral Manifestations of HIV Infection: A Literature Review].Revista cientifica odontologica (Universidad Cientifica del Sur)
    Review
  13. 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 at 5 institutions in 1 country.

Allison B PowellGeorge Washington University Cancer Center, George Washington University, Washington, DC, USA.
Yanqin RenDivision of Infectious Diseases, Weill Cornell Medicine, New York, NY, USA.
Maria KoromGeorge Washington University Cancer Center, George Washington University, Washington, DC, USA.
Devin SaundersCenter for Cancer and Immunology Research, Children's National Medical Center, Washington, DC, USA.
Patrick J HanleyGeorge Washington University Cancer Center, George Washington University, Washington, DC, USA.
Harris GoldsteinDepartment of Pediatrics and Microbiology and Immunology, Albert Einstein College of Medicine, New York, NY, USA.
Douglas F NixonDivision of Infectious Diseases, Weill Cornell Medicine, New York, NY, USA.
Catherine M BollardGeorge Washington University Cancer Center, George Washington University, Washington, DC, USA.
Rebecca M LynchDepartment of Microbiology, Immunology, and Tropical Medicine, George Washington University, Washington, DC, USA.
R Brad JonesDivision of Infectious Diseases, Weill Cornell Medicine, New York, NY, USA.
Conrad Russell Y CruzGeorge Washington University Cancer Center, George Washington University, Washington, DC, USA.
George Washington University · USChildren's National · USCornell University · USAlbert Einstein College of Medicine · USWeill Cornell Medicine · US

Funding

BELIEVE: Bench to Bed Enhanced Lymphocyte Infusions to Engineer Viral EradicationUM1AI126617 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI JONES, R. BRAD, NIXON, DOUGLAS F · 2016 to 2020
$28.1M
The District of Columbia Developmental Center for AIDS Research (DC D-CFAR)P30AI087714 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI GREENBERG, ALAN EDWARD · 2010 to 2014
$8.4M
Engineered CTL with Inducible Ab Secretion; a Tripartite attack on HIV ReservoirsR33AI122391 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI CRUZ, CONRAD RUSSELL YOUNG, JONES, R. BRAD · 2018 to 2020
$1.5M
NIAID NIH HHS P30 AI087714NIAID NIH HHS R33 AI122391NIAID NIH HHS UM1 AI126617
6 · The paper itself

Abstract

While antiretroviral therapy (ART) can completely suppress viremia, it is not a cure for HIV. HIV persists as a latent reservoir of infected cells, able to evade host immunity and re-seed infection following cessation of ART. Two promising immunotherapeutic strategies to eliminate both productively infected cells and reactivated cells of the reservoir are the adoptive transfer of potent HIV-specific T cells and the passive administration of HIV-specific broadly neutralizing antibodies also capable of mediating antibody-dependent cellular cytotoxicity (ADCC). The simultaneous use of both as the basis of a single therapeutic has never been explored. We therefore sought to modify HIV-specific T cells from HIV-naive donors (to allow their use in the context of allotransplant, a promising platform for sterilizing cures) so they are able to secrete a broadly neutralizing antibody (bNAb) directed against the HIV envelope to elicit ADCC. We designed an antibody construct comprising bNAb 10-1074 heavy and light chains, fused to IgG3 Fc to elicit ADCC, with truncated cluster of differentiation 19 (CD19) as a selectable marker. HIV-specific T cells were expanded from HIV-naive donors by priming with antigen-presenting cells expressing overlapping HIV antigens in the presence of cytokines. T cells retained specificity against Gag, Nef, and Pol peptides (218.55 ± 300.14 interferon γ [IFNγ] spot-forming cells [SFC]/1 × 10

Indexed as

antigen-specific T cellsbroadly neutralizing antibodiesHIV

Identifiers

PMID33005704
PMCPMC7508916
OpenAlexW3081275985

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.