Evidence map›Paper›PMID 32303612›Full record

ArticleJournal for immunotherapy of cancer2020

C reactive protein impairs adaptive immunity in immune cells of patients with melanoma.

Tatsuya Yoshida, Junya Ichikawa, Iulia Giuroiu, Andressa S Laino, Yuhan Hao, Michelle Krogsgaard, Melinda Vassallo, David M Woods, F Stephen Hodi, Jeffrey Weber

Erratum issued 2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to 2 registered trials, which are not on this map. Cited by 69 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 3 pooled it
5.4field-weighted citation impact, top 3% 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.

NCT01783938 phase2completednot on this map

An Open-Label, Randomized, Phase 2 Study of Nivolumab Given Sequentially With Ipilimumab in Subjects With Advanced or Metastatic Melanoma

TypeinterventionalSponsorBristol-Myers SquibbRan2013 to 2020Enrolled138ConditionsAdvanced or Metastatic MelanomaArmsNivolumab, Ipilimumab
NCT02983006 phase1completednot on this map

A Phase 1 Study of TRAIL-DR5 Antibody DS-8273a Administered in Combination With Nivolumab in Subjects With Unresectable Stage III or Stage IV Melanoma

TypeinterventionalSponsorNYU Langone HealthRan2016 to 2021Enrolled12ConditionsMelanomaArmsDS-8273a, Nivolumab
3 · Its place in the literature

Who cites it

69 citing papers in PubMed, 3 syntheses or guidelines pooled it, 94 citations in OpenAlex.

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  17. Prognostic utility of the CALLY index in metastatic melanoma: building a nomogram for Patients on Anti-PD-1 therapy.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
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9 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Tatsuya Yoshida *Laura and Isaac Perlmutter Cancer Center, NYU Langone Health, New York, NY, USA.ORCID 0000-0003-4896-5824
Junya Ichikawa *Laura and Isaac Perlmutter Cancer Center, NYU Langone Health, New York, NY, USA.
Iulia GiuroiuLaura and Isaac Perlmutter Cancer Center, NYU Langone Health, New York, NY, USA.
Andressa S LainoLaura and Isaac Perlmutter Cancer Center, NYU Langone Health, New York, NY, USA.
Yuhan HaoCenter for Genomics and Systems Biology, Department of Biology, New York University, New York, NY, USA.
Michelle KrogsgaardLaura and Isaac Perlmutter Cancer Center, NYU Langone Health, New York, NY, USA.
Melinda VassalloLaura and Isaac Perlmutter Cancer Center, NYU Langone Health, New York, NY, USA.
David M WoodsLaura and Isaac Perlmutter Cancer Center, NYU Langone Health, New York, NY, USA.
F Stephen HodiDana-Farber Cancer Institute, Boston, MA, USA.
Jeffrey WeberLaura and Isaac Perlmutter Cancer Center, NYU Langone Health, New York, NY, USA Jeffrey.Weber@nyulangone.org.
NYU Langone Health · USDana-Farber Cancer Institute · USGenomics (United Kingdom) · GB

Funding

Rational Sequencing of PD-1 and CTLA-4 Antibodies in Metastatic MelanomaR01CA175732 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI WEBER, JEFFREY S · 2013 to 2017
$1.7M
Elucidating the Contextual Roles of IL-10 in Patient Response to Cancer ImmunotherapyR00CA230201 · NCI · UNIVERSITY OF COLORADO DENVER · PI WOODS, DAVID MICHAEL · 2020 to 2022
$709k
Elucidating the Contextual Roles of IL-10 in Patient Response to Cancer ImmunotherapyK99CA230201 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI WOODS, DAVID MICHAEL · 2018 to 2019
$274k
NCI NIH HHS K99 CA230201NCI NIH HHS R00 CA230201NCI NIH HHS R01 CA175732
6 · The paper itself

Abstract

backgroundHigh C reactive protein (CRP) levels have been reported to be associated with a poor clinical outcome in a number of malignancies and with programmed cell death protein 1 immune checkpoint blockade in patients with advanced cancer. Little is known about the direct effects of CRP on adaptive immunity in cancer. Therefore, we investigated how CRP impacted the function of T cells and dendritic cells (DCs) from patients with melanoma.

methodsThe effects of CRP on proliferation, function, gene expression and phenotype of patient T cells and DCs, and expansion of MART-1 antigen-specific T cells were analyzed by multicolor flow cytometry and RNA-seq. Additionally, serum CRP levels at baseline from patients with metastatic melanoma treated on the Checkmate-064 clinical trial were assessed by a Luminex assay.

resultsIn vitro, CRP inhibited proliferation, activation-associated phenotypes and the effector function of activated CD4+ and CD8+ T cells from patients with melanoma. CRP-treated T cells expressed high levels of interleukin-1β, which is known to enhance CRP production from the liver. CRP also suppressed formation of the immune synapse and inhibited early events in T-cell receptor engagement. In addition, CRP downregulated the expression of costimulatory molecules on mature DCs and suppressed expansion of MART-1-specific CD8+ T cells in a dose-dependent manner by impacting on both T cells and antigen-presenting cells. High-serum CRP levels at baseline were significantly associated with a shorter survival in both nivolumab-treated and ipilimumab-treated patients.

conclusionsThese findings suggest that high levels of CRP induce an immunosuppressive TRIAL REGISTRATION NUMBER: NCT01783938 and NCT02983006.

Indexed as

Adaptive ImmunityTumor EscapeAcute-Phase ProteinsAdultAntineoplastic Combined Chemotherapy ProtocolsCell ProliferationClinical Trials, Phase II as TopicC-Reactive ProteinDendritic CellsDrug Resistance, NeoplasmFemaleHumansImmune Checkpoint InhibitorsIpilimumabMaleMelanomaAcute-Phase ProteinsC-Reactive ProteinImmune Checkpoint InhibitorsIpilimumabNivolumabimmunologymedicineoncology

Identifiers

PMID32303612
PMCPMC7204799
OpenAlexW3017049470

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.