Evidence map›Paper›PMID 35444059›Full record

ArticleJournal for immunotherapy of cancer2022

Combining bempegaldesleukin (CD122-preferential IL-2 pathway agonist) and NKTR-262 (TLR7/8 agonist) improves systemic antitumor CD8

Annah S Rolig, Daniel C Rose, Grace Helen McGee, Werner Rubas, Saul Kivimäe, William L Redmond

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

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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

6 authors at 3 institutions in 1 country.

Annah S RoligEarle A Chiles Research Institute, Providence Cancer Institute, Portland, OR, USA.ORCID 0000-0001-7080-4352
Daniel C RoseEarle A Chiles Research Institute, Providence Cancer Institute, Portland, OR, USA.
Grace Helen McGeeEarle A Chiles Research Institute, Providence Cancer Institute, Portland, OR, USA.
Werner RubasSutro Biopharma, South San Francisco, CA, USA.
Saul KivimäeNektar Therapeutics, San Francisco, CA, USA.
William L RedmondEarle A Chiles Research Institute, Providence Cancer Institute, Portland, OR, USA william.redmond@providence.org.ORCID 0000-0002-2572-1731
Providence Portland Medical Center · USNektar Therapeutics (United States) · USSutro Biopharma (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTumor cell death caused by radiation therapy (RT) triggers antitumor immunity in part because dying cells release adjuvant factors that amplify and sustain dendritic cell and T cell responses. We previously demonstrated that bempegaldesleukin (BEMPEG: NKTR-214, an immunostimulatory IL-2 cytokine prodrug) significantly enhanced the antitumor efficacy of RT through a T cell-dependent mechanism. Because RT can induce either immunogenic or tolerogenic cell death, depending on various factors (radiation dose, cell cycle phase), we hypothesized that providing a specific immunogenic adjuvant, like intratumoral therapy with a novel toll-like receptor (TLR) 7/8 agonist, NKTR-262, would improve systemic tumor-specific responses through the activation of local innate immunity. Therefore, we evaluated whether intratumoral NKTR-262 combined with systemic BEMPEG treatment would elicit improved tumor-specific immunity and survival compared with RT combined with BEMPEG.

methodsTumor-bearing mice (CT26; EMT6) received BEMPEG (0.8 mg/kg; intravenously), RT (12 Gy × 1), and/or intratumoral NKTR-262 (0.5 mg/kg). Flow cytometry was used to evaluate CD4

resultsBEMPEG+NKTR-262 significantly improved survival compared with BEMPEG+RT in a CD8

conclusionsBEMPEG+NKTR-262 therapy elicited more robust expansion of activated CD8

Indexed as

NeoplasmsToll-Like Receptor 7Adjuvants, ImmunologicAnimalsCD8-Positive T-LymphocytesClinical Trials as TopicHumansImmunotherapyInterleukin-2MiceProgrammed Cell Death 1 ReceptorAdjuvants, ImmunologicInterleukin-2Programmed Cell Death 1 ReceptorTLR7 protein, humanToll-Like Receptor 7Adjuvants, ImmunologicCytokinesImmunotherapyLymphocytes, Tumor-InfiltratingRadiotherapy

Identifiers

PMID35444059
PMCPMC9021762
OpenAlexW4224294761

What OpenQuestion holds

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LicenceCC BY-NC
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.