Evidence map›Paper›PMID 35173157›Full record

ArticleNature communications2022

Early alveolar macrophage response and IL-1R-dependent T cell priming determine transmissibility of Mycobacterium tuberculosis strains.

Arianne Lovey, Sheetal Verma, Vaishnavi Kaipilyawar, Rodrigo Ribeiro-Rodrigues, Seema Husain, Moises Palaci, Reynaldo Dietze, Shuyi Ma, Robert D Morrison, David R Sherman and 2 more

Abstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing 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

44 citing papers in PubMed.

  1. mBio · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Modulation of Ferroptosis During EarlybioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Evaluation of the role ofMicrobiology spectrum · 2025
    Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. 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

12 authors.

Arianne LoveyCenter for Emerging Pathogens, Department of Medicine, Rutgers-New Jersey Medical School, Newark, NJ, USA.ORCID http://orcid.org/0000-0003-0922-1240
Sheetal VermaCenter for Emerging Pathogens, Department of Medicine, Rutgers-New Jersey Medical School, Newark, NJ, USA.
Vaishnavi KaipilyawarCenter for Emerging Pathogens, Department of Medicine, Rutgers-New Jersey Medical School, Newark, NJ, USA.ORCID http://orcid.org/0000-0002-8940-8509
Rodrigo Ribeiro-RodriguesNúcleo de Doenças Infecciosas, NDI/Universidade Federal do Espirito Santo-UFES, Vitoria, Brazil.ORCID http://orcid.org/0000-0002-0675-110X
Seema HusainThe Genomics Center, Rutgers-New Jersey Medical School, Newark, NJ, USA.
Moises PalaciNúcleo de Doenças Infecciosas, NDI/Universidade Federal do Espirito Santo-UFES, Vitoria, Brazil.
Reynaldo DietzeNúcleo de Doenças Infecciosas, NDI/Universidade Federal do Espirito Santo-UFES, Vitoria, Brazil.
Shuyi MaCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, USA.
Robert D MorrisonLaboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD, USA.
David R ShermanDepartment of Microbiology, University of Washington, Seattle, WA, 98109-8070, USA.ORCID http://orcid.org/0000-0003-2185-944X
Jerrold J EllnerCenter for Emerging Pathogens, Department of Medicine, Rutgers-New Jersey Medical School, Newark, NJ, USA.
Padmini SalgameCenter for Emerging Pathogens, Department of Medicine, Rutgers-New Jersey Medical School, Newark, NJ, USA. padmini.salgame@rutgers.edu.ORCID http://orcid.org/0000-0003-2245-3767

Funding

Validation and Application of a Model for Human-like TB Latency in RabbitsU19AI111276 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI ALLAND, DAVID, HORSBURGH, CHARLES ROBERT · 2014 to 2020
$23.3M
Resources, Workforce Development, and Animal Models for the Rutgers RBLUC7AI180307 · NIAID · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI David Alland · 2023 to 2026
$20.1M
Systems Biology CoreU19AI162598 · NIAID · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI RUSSELL, DAVID G · 2021 to 2025
$13.9M
Bacteria and Host in TB TransmissionR01AI147345 · NIAID · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI ALLAND, DAVID, ELLNER, JERROLD J. · 2020 to 2025
$8.7M
US-Brazil Research Collaboration on Strain Variation in TBU01AI065663 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI ELLNER, JERROLD J. · 2005 to 2015
$5.2M
Program in Infection, Immunity and InflammationT32AI125185 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI SALGAME, PADMINI · 2016 to 2020
$747k
NIAID NIH HHS R01 AI147345NIAID NIH HHS T32 AI125185NIAID NIH HHS U01 AI065663NIAID NIH HHS U19 AI111276NIAID NIH HHS U19 AI162598NIAID NIH HHS UC7 AI180307
6 · The paper itself

Abstract

Mechanisms underlying variability in transmission of Mycobacterium tuberculosis strains remain undefined. By characterizing high and low transmission strains of M.tuberculosis in mice, we show here that high transmission M.tuberculosis strain induce rapid IL-1R-dependent alveolar macrophage migration from the alveolar space into the interstitium and that this action is key to subsequent temporal events of early dissemination of bacteria to the lymph nodes, Th1 priming, granulomatous response and bacterial control. In contrast, IL-1R-dependent alveolar macrophage migration and early dissemination of bacteria to lymph nodes is significantly impeded in infection with low transmission M.tuberculosis strain; these events promote the development of Th17 immunity, fostering neutrophilic inflammation and increased bacterial replication. Our results suggest that by inducing granulomas with the potential to develop into cavitary lesions that aids bacterial escape into the airways, high transmission M.tuberculosis strain is poised for greater transmissibility. These findings implicate bacterial heterogeneity as an important modifier of TB disease manifestations and transmission.

Indexed as

AnimalsCell MovementDendritic CellsFemaleLymph NodesLymphocyte ActivationMacrophages, AlveolarMiceMice, Inbred C3HMycobacterium tuberculosisPulmonary AlveoliReceptors, Interleukin-1 Type ISignal TransductionTh17 CellsTh1 CellsTuberculosis, PulmonaryIL1R1 protein, mouseReceptors, Interleukin-1 Type I

Identifiers

PMID35173157
PMCPMC8850437

What OpenQuestion holds

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Registered trials

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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.