Evidence map›Paper›PMID 38563906›Full record

ArticleCancer discovery2024

IL2 Targeted to CD8+ T Cells Promotes Robust Effector T-cell Responses and Potent Antitumor Immunity.

Kelly D Moynihan, Manu P Kumar, Hussein Sultan, Danielle C Pappas, Terrence Park, S Michael Chin, Paul Bessette, Ruth Y Lan, Henry C Nguyen, Nathan D Mathewson and 9 more

Open access · greenAbstract read
In one paragraph

Article in Cancer discovery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
12.3field-weighted citation impact, top 1% 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

46 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  9. Article
  10. Advances in Cancer Immunotherapy for Solid Tumors.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  11. Programmed Cell Death Protein 1-Interleukin-2 Bispecific Agents for Cancer Therapy.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
  12. Article
  13. Article
  14. A modular platform for Sterically Masked Activated Cytokines (SMACks).Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  15. Tumor-targeted IL2 promotes specific CD8Journal of experimental & clinical cancer research : CR · 2026
    Article
  16. Review
  17. Regulators of CD8Nature reviews. Immunology · 2026
    Review
  18. Low-dose IL-2 Ameliorates Experimental Autoimmune Myasthenia Gravis in Rats by Restoring the CD4-positive Helper T-cell Balance Via the JAK/STAT5 Pathway.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2026
    Article
  19. Article
  20. 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

19 authors at 3 institutions in 2 countries.

Kelly D MoynihanAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0000-0001-6200-7863
Manu P KumarAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0000-0002-5506-236X
Hussein SultanDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri.ORCID 0000-0003-4067-8169
Danielle C PappasAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0000-0003-0412-3588
Terrence ParkAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0009-0007-0839-6301
S Michael ChinAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0000-0002-2486-4642
Paul BessetteAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0009-0003-8240-3304
Ruth Y LanAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0000-0002-1898-2271
Henry C NguyenAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0000-0002-6142-8807
Nathan D MathewsonAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0000-0002-8895-2609
Irene NiAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0009-0001-1180-3234
Wei ChenAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0009-0005-3342-1703
Yonghee LeeAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0009-0009-2596-0386
Sindy Liao-ChanAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0000-0002-6606-0247
Jessie ChenAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0009-0008-9170-0243
Ton N M SchumacherDivision of Molecular Oncology and Immunology, Oncode Institute, Netherlands Cancer Institute, Amsterdam; Department of Hematology, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0003-0517-8804
Robert D SchreiberDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri.ORCID 0000-0003-1590-2341
Yik A YeungAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0009-0001-5435-6235
Ivana M DjureticAsher Biotherapeutics, Inc., South San Francisco, California.ORCID 0009-0007-1094-3247
Atara Biotherapeutics (United States) · USWashington University in St. Louis · USLeiden University Medical Center · NL

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI AIMEE S JAMES · 2001 to 2026
$128.0M
National Cancer Institute (NCI) P30 CA91842NCI NIH HHS P30 CA091842
6 · The paper itself

Abstract

IL2 signals pleiotropically on diverse cell types, some of which contribute to therapeutic activity against tumors, whereas others drive undesired activity, such as immunosuppression or toxicity. We explored the theory that targeting of IL2 to CD8+ T cells, which are key antitumor effectors, could enhance its therapeutic index. To this aim, we developed AB248, a CD8 cis-targeted IL2 that demonstrates over 500-fold preference for CD8+ T cells over natural killer and regulatory T cells (Tregs), which may contribute to toxicity and immunosuppression, respectively. AB248 recapitulated IL2's effects on CD8+ T cells in vitro and induced selective expansion of CD8+T cells in primates. In mice, an AB248 surrogate demonstrated superior antitumor activity and enhanced tolerability as compared with an untargeted IL2Rβγ agonist. Efficacy was associated with the expansion and phenotypic enhancement of tumor-infiltrating CD8+ T cells, including the emergence of a "better effector" population. These data support the potential utility of AB248 in clinical settings. Significance: The full potential of IL2 therapy remains to be unlocked. We demonstrate that toxicity can be decoupled from antitumor activity in preclinical models by limiting IL2 signaling to CD8+ T cells, supporting the development of CD8+ T cell-selective IL2 for the treatment of cancer. See related article by Kaptein et al. p. 1226.

Indexed as

CD8-Positive T-LymphocytesInterleukin-2AnimalsCell Line, TumorFemaleHumansMiceNeoplasmsXenograft Model Antitumor AssaysInterleukin-2

Identifiers

PMID38563906
PMCPMC11215410
OpenAlexW4393410341

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.