Evidence map›Paper›PMID 40906897›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2026

CXCR6 promotes dermal CD8+ T cell survival and transition to long-term tissue residence.

Taylor A Heim, Ochapa Ibrahim, Ziyan Lin, Austin C Schultz, Maria M Steele, Tenny Mudianto, Amanda W Lund

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. T-Cell Remodeling in Renal Fibrosis: From Acute Injury to Chronic Kidney Disease.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  2. CXCR6 marks polyfunctional effector CD4 T cells required for anti-bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Single-CellInternational journal of molecular sciences · 2026
    Article
  6. Article
  7. Article
  8. Evolving role of CD8Frontiers in immunology · 2026
    Review
  9. Review
  10. Review
  11. HEB Restrains Effector Gene Expression during Early CD8Molecular and cellular biology · 2025
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Primary nasal viral infection rewires the tissue-scale memory response.bioRxiv : the preprint server for biology · 2024
    Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Taylor A HeimRonald O. Perelman Department of Dermatology, NYU Grossman School of Medicine, New York, NY 10016, United States.ORCID 0000-0003-4128-5754
Ochapa IbrahimRonald O. Perelman Department of Dermatology, NYU Grossman School of Medicine, New York, NY 10016, United States.
Ziyan LinApplied Bioinformatics Laboratories, NYU Langone Health, New York, NY 10016, United States.ORCID 0000-0002-4170-7278
Austin C SchultzRonald O. Perelman Department of Dermatology, NYU Grossman School of Medicine, New York, NY 10016, United States.ORCID 0009-0000-2406-8497
Maria M SteeleRonald O. Perelman Department of Dermatology, NYU Grossman School of Medicine, New York, NY 10016, United States.ORCID 0000-0003-0186-2633
Tenny MudiantoRonald O. Perelman Department of Dermatology, NYU Grossman School of Medicine, New York, NY 10016, United States.
Amanda W LundRonald O. Perelman Department of Dermatology, NYU Grossman School of Medicine, New York, NY 10016, United States.ORCID 0000-0001-7389-9983

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Richard Lewis Possemato · 1985 to 2026
$83.1M
Understanding the origins of rapid recurrence of pancreatic cancer after resectionP30CA069533 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Grace B Gill · 1997 to 2026
$60.5M
cGMP Manufacture, Fill-Finish, Release, Analytical and Stability Testing and Stability Program of a Nanoparticle Based HIV Envelope Vaccine75N93022D00005 · NIAID · INTERNATIONAL AIDS VACCINE INITIATIVE · PI HASSELL, THOMAS · 2022 to 2025
$8.0M
Task Area A shall encompass annual follow-up of cohort members, clinical events investigations, study operations, and data analysis and manuscript writing. If implemented, Task A.1 will provide fundin75N92020D00005 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WATSON, KAROL E · 2020 to 2025
$5.1M
Training Program in Immunology and Inflammation.T32AI100853 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Susan Ruth Schwab · 2012 to 2026
$4.5M
Training in the Molecular Basis of Skin/Mucosa PathobiologyT32CA106195 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI KULESZ-MARTIN, MOLLY F. · 2004 to 2018
$3.8M
Investigating T Cell Egress via Lymphatic Vessels in MelanomaR01CA238163 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI LUND, AMANDA W. · 2019 to 2023
$1.9M
American Cancer Society RSG-18-169-01-LIBCancer Research InstituteFlow Cytometry and Cell Sorting CoreGenome Technology Center SCR_017929Laura and Isaac Perlmutter CancerNCI NIH HHS P30 CA016087NCI NIH HHS P30 CA069533NCI NIH HHS R01 CA238163NCI NIH HHS T32 CA106195NHLBI NIH HHS 75N92020D00005NIAID NIH HHS 75N93022D00005NIAID NIH HHS 75N93023D00005NIAID NIH HHS T32 AI100853NIDA NIH HHS 75N95020D00005NIH HHS P30-CA016087NIH HHS P30CA069533NIH HHS R01CA238163NIH HHS T32AI100853NIH HHS T32CA106195OHSU Knight Cancer CenterORFDO NIH HHS 75N99020D00005
6 · The paper itself

Abstract

Tissue resident memory T cells (TRM) provide protection against local re-infection, and yet the interstitial signals that govern their formation and persistence remain poorly defined. Here, we show that antigen-dependent induction of the chemokine receptor CXCR6, is a conserved adaptation to peripheral tissue infiltration that promotes TRM formation after viral infection. Deficient TRM formation in the absence of CXCR6 was not explained by trafficking as CXCR6 was not required for tissue entry, was dispensable for the early accumulation of antigen-specific CD8+ T cells in skin, and did not restrain their exit. Single cell sequencing indicated that Cxcr6-/- CD8+ T cells were competent to acquire a transcriptional program of residence and TRM that formed were equally functional compared to their WT counterparts when reactivated greater than 100 days post primary infection. The reduction in Cxcr6-/- CD8+ T cells at memory time points, was associated with impaired redox homeostasis, antioxidant capacity, and increased rates of apoptosis in the dermis during the transition from effector to resident memory. Thus, CXCR6 promotes the adaptation of T cells as they engage antigen in tissue to increase the probability of survival, memory differentiation, and long-term residence.

Indexed as

CD8-Positive T-LymphocytesDermisMemory T CellsReceptors, CXCR6SkinAnimalsCell SurvivalImmunologic MemoryMiceMice, Inbred C57BLMice, KnockoutCxcr6 protein, mouseReceptors, CXCR6CXCR6resident memory T cellsskintraffickingvaccinia virus

Identifiers

PMID40906897
PMCPMC12412903

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.