Evidence map›Paper›PMID 35298559›Full record

ArticlePloS one2022

A TCR mimic monoclonal antibody for the HPV-16 E7-epitope p11-19/HLA-A*02:01 complex.

Tao Dao, Sungsoo Mun, Tatyana Korontsvit, Abdul G Khan, Mary Ann Pohl, Thomas White, Martin G Klatt, David Andrew, Ivo C Lorenz, David A Scheinberg

Abstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. NK cells in HPV-related tumorigenesis: mechanisms and clinical applications.Frontiers in cellular and infection microbiology · 2025
    Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. 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.

Tao DaoMolecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.ORCID 0000-0001-9937-6283
Sungsoo MunMolecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
Tatyana KorontsvitMolecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
Abdul G KhanTri-Institutional Therapeutics Discovery Institute, New York, New York, United States of America.
Mary Ann PohlTri-Institutional Therapeutics Discovery Institute, New York, New York, United States of America.
Thomas WhiteTri-Institutional Therapeutics Discovery Institute, New York, New York, United States of America.
Martin G KlattMolecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.ORCID 0000-0001-8703-7305
David AndrewTri-Institutional Therapeutics Discovery Institute, New York, New York, United States of America.
Ivo C LorenzTri-Institutional Therapeutics Discovery Institute, New York, New York, United States of America.ORCID 0000-0002-7373-1176
David A ScheinbergMolecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
T LYMPHOCYTE SUBSET FUNCTION POST-TRANSPLANTATIONP01CA023766 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SCHEINBERG, DAVID A · 1985 to 2023
$59.0M
Understanding and Mimicking TCR Recognition with Therapeutic Monoclonal Antibodies.R35CA241894 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI DAVID A SCHEINBERG · 2020 to 2026
$7.2M
RECOMBINANT ANTICD33 ANTIBODY FOR AMLR01CA055349 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SCHEINBERG, DAVID A · 1991 to 2020
$6.8M
Developing therapeutic TCR mimic monoclonal antibodies for cancerR50CA265328 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Tao Dao · 2022 to 2026
$676k
NCI NIH HHS P01 CA023766NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA055349NCI NIH HHS R35 CA241894NCI NIH HHS R50 CA265328
6 · The paper itself

Abstract

More effective treatments are needed for human papilloma virus (HPV)-induced cancers despite HPV virus vaccination. The oncogenic HPV protein targets are currently undruggable and intracellular and therefore there are no antibodies to these targets. Here we report the discovery of TCR mimic monoclonal antibodies (TCRm mAb) specific for the HPV E7 protein p11-19, YMLDLQPET, when presented on the cell surface in the context of HLA-A*02:01 by use of human phage display libraries. One of the mAbs, 3F8, was able to specifically mediate T cell- redirected cytotoxicity, in a bispecific T cell engager (BiTE) form. While further studies are required to assess the therapeutic potential of this approach, the study provided the proof of concept that TCRm mAb could be a therapeutic strategy for HPV-induced human cancers.

Indexed as

Antineoplastic Agents, ImmunologicalNeoplasmsOncogene Proteins, ViralPapillomavirus InfectionsAntibodies, MonoclonalEpitopesHLA-A AntigensHuman papillomavirus 16HumansPapillomavirus E7 ProteinsReceptors, Antigen, T-CellAntibodies, MonoclonalAntineoplastic Agents, ImmunologicalEpitopesHLA-A AntigensOncogene Proteins, ViralPapillomavirus E7 ProteinsReceptors, Antigen, T-Cell

Identifiers

PMID35298559
PMCPMC8929633

What OpenQuestion 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 OpenQuestion graph.