Evidence map›Paper›PMID 42785956›Full record

ArticleLife science alliance2026

Murine IL-2 outperforms human IL-2 in supporting the survival of naïve mouse CD8 T cells in vitro.

Yangle Yu, Tete I Obot, Madaleine M Niznikiewicz, Craig M Podszus, Julio S Dos-Santos, Elena L Pobezinskaya, Priyadharshini Devarajan, Leonid A Pobezinsky, Brian S Sheridan

Abstract read
In one paragraph

Article in Life science alliance, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Yangle YuDepartment of Microbiology and Immunology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.ORCID https://orcid.org/0009-0007-7578-1920
Tete I ObotDepartment of Microbiology and Immunology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.
Madaleine M NiznikiewiczDepartment of Microbiology and Immunology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.
Craig M PodszusDepartment of Microbiology and Immunology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.
Julio S Dos-SantosDepartment of Microbiology and Immunology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.
Elena L PobezinskayaDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA, USA.ORCID https://orcid.org/0000-0001-6408-8732
Priyadharshini DevarajanDepartment of Microbiology and Immunology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.
Leonid A PobezinskyDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA, USA.ORCID https://orcid.org/0000-0002-6115-3559
Brian S SheridanDepartment of Microbiology and Immunology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA brian.sheridan@stonybook.edu.ORCID https://orcid.org/0000-0002-3299-5888

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008444 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI FROHMAN, MICHAEL A. · 1992 to 2024
$12.6M
MOLECULAR AND CELL BIOLOGY OF INFECTIOUS DISEASEST32AI007539 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI KONOPKA, JAMES B · 1998 to 2023
$3.6M
Impact of priming on the generation of intestinal tissue-resident memory T cellsR01AI172919 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI Brian S Sheridan · 2022 to 2026
$2.5M
IMSD at Stony Brook University: Maximizing Excellence in Research for Graduate Education -- Fostering Inclusive Research Scientist Training (FIRST)T32GM135746 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI GERGEN, JOHN PETER · 2021 to 2025
$2.3M
Scholars in BioMedical Sciences (SBMS) Training ProgramT32GM148331 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI Styliani-Anna (Stella) E Tsirka · 2024 to 2026
$695k
NIAID NIH HHS R01 AI172919NIAID NIH HHS T32 AI007539NIGMS NIH HHS T32 GM008444NIGMS NIH HHS T32 GM135746NIGMS NIH HHS T32 GM148331
6 · The paper itself

Abstract

Much of the immunology community relies on human IL-2 to support murine CD8 T-cell expansion in vitro. Although human and murine IL-2 share high similarity in amino acid sequence and exhibit similar biological activity, the potential cross-species implications of this practice remain largely unexamined, representing a significant yet overlooked variable in many in vitro studies that serve as the foundation of T-cell biology. Here, we compared the effects of human and murine IL-2 on CD8 T cells in vitro to uncover potential differences in T-cell biology. Murine IL-2 more effectively supported the survival of mouse naïve CD8 T cells in vitro and induced a distinct phenotype of IL-2 receptor expression on activated mouse CD8 T cells. In addition, murine IL-2 promoted enhanced antigen-independent expansion of memory-like CD8 T cells from naïve animals. Collectively, these findings should encourage laboratories to reevaluate their human IL-2 dosing strategies or consider transitioning to murine IL-2 for in vitro studies using murine CD8 T cells.

Indexed as

CD8-Positive T-LymphocytesInterleukin-2AnimalsCell ProliferationCell SurvivalHumansLymphocyte ActivationMiceMice, Inbred C57BLReceptors, Interleukin-2Interleukin-2Receptors, Interleukin-2

Identifiers

PMID42785956
PMCPMC13613269

What OpenQuestion holds

Textmetadata
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.