Evidence map›Paper›PMID 35053490›Full record

ArticleCancers2022

Nicotinamide Inhibits T Cell Exhaustion and Increases Differentiation of CD8 Effector T Cells.

Sara Alavi, Abdullah Al Emran, Hsin-Yi Tseng, Jessamy C Tiffen, Helen Marie McGuire, Peter Hersey

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
  2. NAD + metabolism and function in innate and adaptive immune cells.Journal of inflammation (London, England) · 2025
    Review
  3. Mitochondrial Metabolism in T-Cell Exhaustion.International journal of molecular sciences · 2025
    Review
  4. Article
  5. Review
  6. X and Y Differences in Melanoma Survival Between the Sexes.Pigment cell & melanoma research · 2025
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Effects of nicotinamide on follicular development and the quality of oocytes.Reproductive biology and endocrinology : RB&E · 2022
    Article
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

6 authors at 1 institution in 2 countries.

Sara AlaviMelanoma Immunology and Oncology Program, The Centenary Institute, University of Sydney, Camperdown 2050, Australia.
Abdullah Al EmranMelanoma Immunology and Oncology Program, The Centenary Institute, University of Sydney, Camperdown 2050, Australia.ORCID 0000-0001-5518-6605
Hsin-Yi TsengMelanoma Immunology and Oncology Program, The Centenary Institute, University of Sydney, Camperdown 2050, Australia.ORCID 0000-0002-7499-7515
Jessamy C TiffenMelanoma Immunology and Oncology Program, The Centenary Institute, University of Sydney, Camperdown 2050, Australia.
Helen Marie McGuireMelanoma Immunology and Oncology Program, The Centenary Institute, University of Sydney, Camperdown 2050, Australia.ORCID 0000-0003-2047-6543
Peter HerseyMelanoma Immunology and Oncology Program, The Centenary Institute, University of Sydney, Camperdown 2050, Australia.
The University of Sydney · AU

Funding

Cancer Council NSW RG18/10Cancer Council NSW RG28/12Centenary Institute support grant NANational Health and Medical Research Council APP1093017
6 · The paper itself

Abstract

One of the limitations of immunotherapy is the development of a state referred to as T cell exhaustion (TEx) whereby T cells express inhibitory receptors (IRs) and lose production of effectors involved in killing of their targets. In the present studies we have used the repeated stimulation model with anti CD3 and anti CD28 to understand the factors involved in TEx development and treatments that may reduce changes of TEx. The results show that addition of nicotinamide (NAM) involved in energy supply to cells prevented the development of inhibitory receptors (IRs). This was particularly evident for the IRs CD39, TIM3, and to a lesser extent LAG3 and PD1 expression. NAM also prevented the inhibition of IL-2 and TNFα expression in TEx and induced differentiation of CD4+ and CD8 T cells to effector memory and terminal effector T cells. The present results showed that effects of NAM were linked to regulation of reactive oxygen species (ROS) consistent with previous studies implicating ROS in upregulation of TOX transcription factors that induce TEx. These effects of NAM in reducing changes of TEx and in increasing the differentiation of T cells to effector states appears to have important implications for the use of NAM supplements in immunotherapy against cancers and viral infections and require further exploration in vivo.

Indexed as

epigeneticsEZH2inhibitory receptorsmetabolismnicotinamideT cell exhaustionTOX

Identifiers

PMID35053490
PMCPMC8774026
OpenAlexW4205484745

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.