Evidence map›Paper›PMID 36405684›Full record

ReviewFrontiers in immunology2022

NKB cells: A double-edged sword against inflammatory diseases.

Nikunj Tandel, Sushmita Negi, Rajeev K Tyagi

Open access · goldAbstract readReview
In one paragraph

Review 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Single-Cell RNA-seq Analysis Reveals Distinct Tumor and Immunosuppressive T-Cell Phenotypes in Patients with CLL Treated with Ibrutinib.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  3. Observational
  4. Article
  5. Article
  6. 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

3 authors at 2 institutions in 1 country.

Nikunj TandelInstitute of Science, Nirma University, Ahmedabad, Gujarat, India.
Sushmita NegiDivision of Cell Biology and Immunology, Biomedical Parasitology and Nano-immunology Lab, Council of Scientific and Industrial Research (CSIR)-Institute of Microbial Technology (IMTECH), Chandigarh, India.
Rajeev K TyagiDivision of Cell Biology and Immunology, Biomedical Parasitology and Nano-immunology Lab, Council of Scientific and Industrial Research (CSIR)-Institute of Microbial Technology (IMTECH), Chandigarh, India.
Institute of Microbial Technology · INNirma University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interferon-γ (IFN-γ)-producing natural killer (NK) cells and innate lymphoid cells (ILCs) activate the adaptive system's B and T cells in response to pathogenic invasion; however, how these cells are activated during infections is not yet fully understood. In recent years, a new lymphocyte population referred to as "natural killer-like B (NKB) cells", expressing the characteristic markers of innate NK cells and adaptive B cells, has been identified in both the spleen and mesenteric lymph nodes during infectious and inflammatory pathologies. NKB cells produce IL-18 and IL-12 cytokines during the early phases of microbial infection, differentiating them from conventional NK and B cells. Emerging evidence indicates that NKB cells play key roles in clearing microbial infections. In addition, NKB cells contribute to inflammatory responses during infectious and inflammatory diseases. Hence, the role of NKB cells in disease pathogenesis merits further study. An in-depth understanding of the phenotypic, effector, and functional properties of NKB cells may pave the way for the development of improved vaccines and therapeutics for infectious and inflammatory diseases.

Indexed as

Immunity, InnateKiller Cells, NaturalCytokinesInterleukin-12Lymphocyte SubsetsCytokinesInterleukin-12IFN-γIL-12IL-18infectious diseasesinflammationinnate lymphoid cellsNKB cellsTh1 cells

Identifiers

PMID36405684
PMCPMC9669376
OpenAlexW4308068247

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.