Evidence map›Paper›PMID 36512052›Full record

ArticleCancer immunology research2023

Self-Renewing CD8+ T-cell Abundance in Blood Associates with Response to Immunotherapy.

Rohan Maniar, Peter H Wang, Robert S Washburn, Radomir Kratchmarov, Shana M Coley, Anjali Saqi, Samuel S Pan, Jianhua Hu, Catherine A Shu, Naiyer A Rizvi and 2 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology research, 2023. 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 18% 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, 18 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Increased Peripheral T Stem Cell-like Memory Features in Patients with Advanced Solid Tumors Treated with Tumor-Targeting IL-12 Immunocytokine Therapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  5. Article
  6. Review
  7. Mechanisms of primary resistance to immune checkpoint inhibitors in NSCLC.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  8. Circulating memory T cells and TCF1Journal of pharmaceutical analysis · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. The expanding Pandora's toolbox of CD8Journal of translational medicine · 2023
    Review
  13. Article
  14. Article
  15. Dynamic change of CD8Translational lung cancer research · 2023
    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

12 authors at 2 institutions in 1 country.

Rohan ManiarDivision of Hematology & Oncology, Columbia University Irving Medical Center, New York, New York.ORCID 0000-0002-6089-2237
Peter H WangDepartment of Microbiology and Immunology, Columbia University Irving Medical Center, New York, New York.ORCID 0000-0002-5922-5111
Robert S WashburnDepartment of Microbiology and Immunology, Columbia University Irving Medical Center, New York, New York.ORCID 0000-0002-3533-951X
Radomir KratchmarovDepartment of Microbiology and Immunology, Columbia University Irving Medical Center, New York, New York.ORCID 0000-0002-6796-8564
Shana M ColeyDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York.ORCID 0000-0002-2152-5469
Anjali SaqiDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York.ORCID 0000-0003-3133-9886
Samuel S PanDepartment of Biostatistics, Mailman School of Public Health, Columbia University, New York, New York.ORCID 0000-0002-2860-0855
Jianhua HuDepartment of Biostatistics, Mailman School of Public Health, Columbia University, New York, New York.ORCID 0000-0002-3306-6722
Catherine A ShuDivision of Hematology & Oncology, Columbia University Irving Medical Center, New York, New York.ORCID 0000-0003-0765-7665
Naiyer A RizviDivision of Hematology & Oncology, Columbia University Irving Medical Center, New York, New York.ORCID 0000-0002-1134-7494
Brian S HenickDivision of Hematology & Oncology, Columbia University Irving Medical Center, New York, New York.ORCID 0000-0003-2681-0805
Steven L ReinerDepartment of Microbiology and Immunology, Columbia University Irving Medical Center, New York, New York.ORCID 0000-0002-1635-8619
Columbia University Irving Medical Center · USNew York University · US

Funding

Molecular Oncology Training ProgramT32CA203703 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Katherine D Crew, DAWN HERSHMAN · 2016 to 2026
$4.1M
Asymmetric Lymphocyte Division in the Immune ResponseR01AI076458 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI REINER, STEVEN L · 2008 to 2019
$3.7M
Strategies to predict and overcome resistance to cancer immunotherapyR01CA279268 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI STEVEN L REINER · 2023 to 2026
$2.2M
Columbia University Graduate Training Program in Microbiology and ImmunologyT32AI106711 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Nicholas Arpaia, Uttiya Basu · 2014 to 2026
$2.1M
Self-renewing Lymphocyte Division in The Immune ResponseR56AI076458 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI REINER, STEVEN L · 2014 to 2021
$802k
NCI NIH HHS R01 CA279268NCI NIH HHS T32 CA203703NIAID NIH HHS R01 AI076458NIAID NIH HHS R56 AI076458NIAID NIH HHS T32 AI106711
6 · The paper itself

Abstract

Treatment with immune checkpoint blockade (ICB) often fails to elicit durable antitumor immunity. Recent studies suggest that ICB does not restore potency to terminally dysfunctional T cells, but instead drives proliferation and differentiation of self-renewing progenitor T cells into fresh, effector-like T cells. Antitumor immunity catalyzed by ICB is characterized by mobilization of antitumor T cells in systemic circulation and tumor. To address whether abundance of self-renewing T cells in blood is associated with immunotherapy response, we used flow cytometry of peripheral blood from a cohort of patients with metastatic non-small cell lung cancer (NSCLC) treated with ICB. At baseline, expression of T-cell factor 1 (TCF1), a marker of self-renewing T cells, was detected at higher frequency in effector-memory (CCR7-) CD8+ T cells from patients who experienced durable clinical benefit compared to those with primary resistance to ICB. On-treatment blood samples from patients benefiting from ICB also exhibited a greater frequency of TCF1+CCR7-CD8+ T cells and higher proportions of TCF1 expression in treatment-expanded PD-1+CCR7-CD8+ T cells. The observed correlation of TCF1 frequency in CCR7-CD8+ T cells and response to ICB suggests that broader examination of self-renewing T-cell abundance in blood will determine its potential as a noninvasive, predictive biomarker of response and resistance to immunotherapy.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsCD8-Positive T-LymphocytesHumansImmunotherapyReceptors, CCR7Receptors, CCR7

Identifiers

PMID36512052
PMCPMC9898128
OpenAlexW4311291259

What OpenQuestion holds

Textmetadata
LicenceTDM
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.