Evidence map›Paper›PMID 31719059›Full record

ArticleCancer immunology research2020

Pathogen-Boosted Adoptive Cell Transfer Therapy Induces Endogenous Antitumor Immunity through Antigen Spreading.

Gang Xin, Achia Khatun, Paytsar Topchyan, Ryan Zander, Peter J Volberding, Yao Chen, Jian Shen, Chunmei Fu, Aimin Jiang, William A See and 1 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. XCL1-secreting CEA CAR-T cells enhance endogenous CD8Journal for immunotherapy of cancer · 2025
    Article
  4. Review
  5. Review
  6. Article
  7. Cytokine conjugation to enhance T cell therapy.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Frontiers in immunology · 2023
    Review
  9. Review
  10. T cell help in the autoreactive germinal center.Scandinavian journal of immunology · 2022
    Review
  11. Th1-Dominant CD4Frontiers in immunology · 2022
    Article
  12. Article
  13. Review
  14. Article
  15. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Gang XinBlood Research Institute, Blood Center of Wisconsin, Milwaukee, Wisconsin.
Achia KhatunBlood Research Institute, Blood Center of Wisconsin, Milwaukee, Wisconsin.
Paytsar TopchyanBlood Research Institute, Blood Center of Wisconsin, Milwaukee, Wisconsin.
Ryan ZanderBlood Research Institute, Blood Center of Wisconsin, Milwaukee, Wisconsin.
Peter J VolberdingBlood Research Institute, Blood Center of Wisconsin, Milwaukee, Wisconsin.
Yao ChenBlood Research Institute, Blood Center of Wisconsin, Milwaukee, Wisconsin.
Jian ShenBlood Research Institute, Blood Center of Wisconsin, Milwaukee, Wisconsin.ORCID 0000-0001-8398-2318
Chunmei FuDepartment of Immunology, Roswell Park Cancer Institute, Buffalo, New York.
Aimin JiangDepartment of Immunology, Roswell Park Cancer Institute, Buffalo, New York.
William A SeeDepartment of Urology, Medical College of Wisconsin, Milwaukee, Wisconsin.
Weiguo CuiBlood Research Institute, Blood Center of Wisconsin, Milwaukee, Wisconsin. weiguo.cui@bcw.edu.
Medical College of Wisconsin · USRoswell Park Comprehensive Cancer Center · USVersiti Blood Center of Wisconsin · US

Funding

Medical Scientist Training ProgramT32GM080202 · NIGMS · MEDICAL COLLEGE OF WISCONSIN · PI BARBIERI, JOSEPH T, SALZMAN, NITA H · 2010 to 2024
$5.7M
The Cellular and Transcriptional Control of CD8 T Cell Functional Adaptation to Chronic VirusesR01AI125741 · NIAID · VERSITI WISCONSIN, INC. · PI CUI, WEIGUO · 2016 to 2020
$2.1M
b-catenin in vaccine-induced anti-tumor CD8 T cell immunityR01CA198105 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI JIANG, AIMIN · 2015 to 2019
$2.0M
NCI NIH HHS R01 CA198105NIAID NIH HHS R01 AI125741NIGMS NIH HHS T32 GM080202
6 · The paper itself

Abstract

Loss of target antigens in tumor cells has become one of the major hurdles limiting the efficacy of adoptive cell therapy (ACT)-based immunotherapies. The optimal approach to overcome this challenge includes broadening the immune response from the initially targeted tumor-associated antigen (TAA) to other TAAs expressed in the tumor. To induce a more broadly targeted antitumor response, we utilized our previously developed Re-energized ACT (ReACT), which capitalizes on the synergistic effect of pathogen-based immunotherapy and ACT. In this study, we showed that ReACT induced a sufficient endogenous CD8

Indexed as

AnimalsAntigens, NeoplasmCD8-Positive T-LymphocytesCell Line, TumorFemalegp100 Melanoma AntigenImmunologic MemoryImmunotherapy, AdoptiveListeria monocytogenesListeriosisMelanoma, ExperimentalMiceMice, Inbred C57BLSkin NeoplasmsAntigens, Neoplasmgp100 Melanoma Antigen

Identifiers

PMID31719059
PMCPMC6946848
OpenAlexW2984410235

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.