Evidence map›Paper›PMID 37400134›Full record

ArticleJournal for immunotherapy of cancer2023

Combination of cancer vaccine with CD122-biased IL-2/anti-IL-2 Ab complex shapes the stem-like effector NK and CD8

Kanako Shimizu, Shogo Ueda, Masami Kawamura, Honoka Aoshima, Mikiko Satoh, Jun Nakabayashi, Shin-Ichiro Fujii

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Stem-like CD8Frontiers in immunology · 2024
    Review
  4. Review
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

7 authors at 2 institutions in 1 country.

Kanako ShimizuLaboratory for Immunotherapy, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Shogo UedaLaboratory for Immunotherapy, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Masami KawamuraLaboratory for Immunotherapy, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Honoka AoshimaLaboratory for Immunotherapy, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Mikiko SatohLaboratory for Immunotherapy, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Jun NakabayashiDepartment of Mathematics, Tokyo Medical and Dental University, Ichikawa, Japan.
Shin-Ichiro FujiiLaboratory for Immunotherapy, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan shin-ichiro.fujii@riken.jp.ORCID http://orcid.org/0000-0003-3586-3976
RIKEN Center for Integrative Medical Sciences · JPTokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA key to success of cancer immunotherapy is the amplification and sustenance of various effector cells. The hallmark of prominent antitumor T cells is their long-term effector function. Although interleukin (IL)-2 is an attractive cytokine, several attempts have been made towards developing IL-2 modalities with improved effectiveness and safety that enhance natural killer (NK) cells or T cells in cancer models. However, whether such IL-2 modalities can simultaneously support long-term innate and adaptive immunity, particularly stem-like memory, has not been shown. To resolve this issue, we compared the antitumor cellular mechanism with two IL-2/anti-IL-2 complexes (IL-2Cxs) administered in combination with a therapeutic cancer vaccine, which we had previously established as an in vivo dendritic cell-targeting therapy.

methodsTwo types of IL-2Cxs, CD25-biased IL-2Cx and CD122-biased IL-2Cx, together with a Wilms' tumor 1-expressing vaccine, were evaluated in a leukemic model. The immunological response and synergistic antitumor efficacy of these IL-2Cxs were then evaluated.

resultsWhen CD25-biased or CD122-biased IL-2Cxs in combination with the vaccine were assessed in an advanced-leukemia model, the CD122-biased IL-2Cx combination showed 100% survival, but the CD25-biased IL-2Cx did not. We first showed that invariant natural killer T (NKT) 1 cells are predominantly activated by CD122-biased IL-2Cx. In addition, in-depth analysis of immune responses by CD122-biased IL-2Cx in lymphoid tissues and the tumor microenvironment revealed a dramatic increase in the distinct subsets of NK and CD8

conclusionsCD122-biased IL-2Cx combined with the vaccine can induce a series of reactions in the immune cascade, including activation of not only NKT1 cells, but also NK and CD8

Indexed as

Cancer VaccinesNeoplasmsCD8-Positive T-LymphocytesCytokinesHumansKiller Cells, NaturalTumor MicroenvironmentCancer VaccinesCytokinesCD8-Positive T-LymphocytesCytokinesImmunologic MemoryKiller Cells, NaturalNatural Killer T-Cells

Identifiers

PMID37400134
PMCPMC10577731
OpenAlexW4382931117

What OpenQuestion holds

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LicenceCC BY-NC
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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.