Evidence map›Paper›PMID 35250975›Full record

ArticleFrontiers in immunology2022

Increased Expression of Tim-3 Is Associated With Depletion of NKT Cells In SARS-CoV-2 Infection.

Jingzhi Yang, Teding Chang, Liangsheng Tang, Hai Deng, Deng Chen, Jialiu Luo, Han Wu, TingXuan Tang, Cong Zhang, Zhenwen Li and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. TIM-3, a potential target for sepsis therapy.Chinese journal of traumatology = Zhonghua chuang shang za zhi · 2026
    Review
  2. TIM-3+ Macrophages: Insights into Their Role in Cancer and Inflammation.International journal of molecular sciences · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Multi‑omics reveal neutrophil heterogeneity in sepsis (Review).International journal of molecular medicine · 2025
    Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. CAR-NKT Cells in Asthma: Use of NKT as a Promising Cell for CAR Therapy.Clinical reviews in allergy & immunology · 2024
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. 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

13 authors at 3 institutions in 1 country.

Jingzhi YangDivision of Trauma & Surgical Critical Care, Department of Surgery, Tongji Hospital, Wuhan, China.
Teding ChangDivision of Trauma & Surgical Critical Care, Department of Surgery, Tongji Hospital, Wuhan, China.
Liangsheng TangDivision of Trauma & Surgical Critical Care, Department of Surgery, Tongji Hospital, Wuhan, China.
Hai DengDivision of Trauma & Surgical Critical Care, Department of Surgery, Tongji Hospital, Wuhan, China.
Deng ChenDivision of Trauma & Surgical Critical Care, Department of Surgery, Tongji Hospital, Wuhan, China.
Jialiu LuoDivision of Trauma & Surgical Critical Care, Department of Surgery, Tongji Hospital, Wuhan, China.
Han WuDivision of Trauma & Surgical Critical Care, Department of Surgery, Tongji Hospital, Wuhan, China.
TingXuan TangSchool of Medicine, Wuhan University of Science and Technology, Wuhan, China.
Cong ZhangDivision of Trauma & Surgical Critical Care, Department of Surgery, Tongji Hospital, Wuhan, China.
Zhenwen LiDivision of Trauma & Surgical Critical Care, Department of Surgery, Tongji Hospital, Wuhan, China.
Liming DongDivision of Trauma & Surgical Critical Care, Department of Surgery, Tongji Hospital, Wuhan, China.
Xiang-Ping YangDepartment of Immunology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Zhao-Hui TangDivision of Trauma & Surgical Critical Care, Department of Surgery, Tongji Hospital, Wuhan, China.
Tongji Hospital · CNHuazhong University of Science and Technology · CNWuhan University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the ongoing coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), natural killer T (NKT) cells act as primary initiators of immune responses. However, a decrease of circulating NKT cells has been observed in COVID-19 different stages, of which the underlying mechanism remains to be elucidated. Here, by performing single-cell RNA sequencing analysis in three large cohorts of COVID-19 patients, we found that increased expression of Tim-3 promotes depletion of NKT cells during the progression stage of COVID-19, which is associated with disease severity and outcome of patients with COVID-19. Tim-3+ NKT cells also expressed high levels of CD147 and CD26, which are potential SARS-CoV-2 spike binding receptors. In the study, Tim-3+ NKT cells showed high enrichment of apoptosis, higher expression levels of mitochondrial genes and caspase genes, with a larger pseudo time value. In addition, Tim-3+ NKT cells in COVID-19 presented a stronger capacity to secrete IFN-γ, IL-4 and IL-10 compared with healthy individuals, they also demonstrated high expression of co-inhibitory receptors such as PD-1, CTLA-4, and LAG-3. Moreover, we found that IL-12 secreted by dendritic cells (DCs) was positively correlated with up-regulated expression of Tim-3 in NKT cells in COVID-19 patients. Overall, this study describes a novel mechanism by which up-regulated Tim-3 expression induced the depletion and dysfunction of NKT cells in COVID-19 patients. These findings not only have possible implications for the prediction of severity and prognosis in COVID-19 but also provide a link between NKT cells and future new therapeutic strategies in SARS-CoV-2 infection.

Indexed as

COVID-19Hepatitis A Virus Cellular Receptor 2HumansInterferon-gammaInterleukin-10Interleukin-4Natural Killer T-CellsSARS-CoV-2Signal TransductionHAVCR2 protein, humanHepatitis A Virus Cellular Receptor 2Interferon-gammaInterleukin-10Interleukin-4COVID-19immunopathogenesisNKT cellsscRNA-SeqTim-3

Identifiers

PMID35250975
PMCPMC8889099
OpenAlexW4213195895

What OpenQuestion holds

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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.