Evidence map›Paper›PMID 35069548›Full record

ArticleFrontiers in immunology2021

Dynamics of Macrophage, T and B Cell Infiltration Within Pulmonary Granulomas Induced by

Laura Hunter, Suzie Hingley-Wilson, Graham R Stewart, Sally A Sharpe, Francisco Javier Salguero

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.7field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 28 citations in OpenAlex.

  1. Tuberculosis in Pregnancy: Challenges of Immune Protection.The Journal of infectious diseases · 2026
    Review
  2. HowVaccines · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Building Spatiotemporal Understanding ofACS infectious diseases · 2025
    Review
  11. Spatial Patterning Analysis of Cellular Ensembles (SPACE) finds complex spatial organization at the cell and tissue levels.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Article
  13. Identification ofAnnals of medicine · 2024
    Article
  14. Review
  15. B Cell and Antibody Responses in Bovine Tuberculosis.Antibodies (Basel, Switzerland) · 2024
    Review
  16. Article
  17. Article
  18. Characterizing the immune response toFrontiers in immunology · 2024
    Review
  19. Article
  20. 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

5 authors at 2 institutions in 1 country.

Laura HunterResearch and Evaluation, UK Health Security Agency (UKHSA), Salisbury, United Kingdom.
Suzie Hingley-WilsonSchool of Biosciences and Medicine, University of Surrey, Guildford, United Kingdom.
Graham R StewartSchool of Biosciences and Medicine, University of Surrey, Guildford, United Kingdom.
Sally A SharpeResearch and Evaluation, UK Health Security Agency (UKHSA), Salisbury, United Kingdom.
Francisco Javier SalgueroResearch and Evaluation, UK Health Security Agency (UKHSA), Salisbury, United Kingdom.
University of Surrey · GBUK Health Security Agency

Funding

Department of HealthMedical Research Council MR/N007328/1Medical Research Council MR/T028998/1
6 · The paper itself

Abstract

Non-human primate models of Tuberculosis (TB) are one of the most commonly used within the experimental TB field because they closely mimic the whole spectrum of disease progression of human TB. However, the early cellular interactions of the pulmonary granuloma are still not well understood. The use of this model allows investigation into the early interactions of cells within pulmonary granulomas which cannot be undertaken in human samples. Pulmonary granulomas from rhesus and cynomolgus macaques from two timepoints post infection were categorised into categories 1 - 6 (early to late stage granulomas) and immunohistochemistry was used to identify CD68+ macrophages, CD3+ T cells and CD20+ B cells. Multinucleated giant cells and acid-fast bacilli were also quantified. At week four post infection, cynomolgus macaques were found to have more CD68+ cells than rhesus in all but category 1 granulomas. Cynomolgus also had a significantly higher percentage of CD20+ B cells in category 1 granulomas. At week twelve post infection, CD68+ cells were most abundant in category 4 and 5 granulomas in both species; however, there were no significant differences between them. CD3+ T cells and CD20+ B cells were significantly higher in the majority of granuloma categories in cynomolgus compared to rhesus. Multinucleated giant cells and acid-fast bacilli were most abundant in categories 5 and 6 at week 12 post challenge in both species. This study has identified the basic cellular composition and spatial distribution of immune cells within pulmonary granulomas in both rhesus and cynomolgus macaques over time. The data from this study will add to the knowledge already gained in this field and may inform future research on vaccines and therapeutics for TB.

Indexed as

B-LymphocytesCD8-Positive T-LymphocytesGranulomaMacrophagesTuberculosis, PulmonaryAnimalsDisease Models, AnimalMacaca fascicularisMacaca mulattaMycobacterium tuberculosiscynomolgus macaqueimmunohistochemistrylymphocytemacrophagepathologypulmonary granulomarhesus macaquetuberculosis

Identifiers

PMID35069548
PMCPMC8770544
OpenAlexW4206610399

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.