Evidence map›Paper›PMID 28686604›Full record

ArticlePloS one2017

Boosting efferocytosis in alveolar space using BCG vaccine to protect host against influenza pneumonia.

Sanjay Mukherjee, Renuka Subramaniam, Han Chen, Anthony Smith, Shiva Keshava, Homayoun Shams

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

42 citing papers in PubMed, 69 citations in OpenAlex.

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  11. Interstitial Macrophages Mediate Efferocytosis of Alveolar Epithelium during Influenza Infection.American journal of respiratory cell and molecular biology · 2024
    Article
  12. Article
  13. Efferocytosis and Respiratory Disease.International journal of molecular sciences · 2023
    Review
  14. Article
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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 1 country.

Sanjay MukherjeeCenter for Pulmonary and Infectious Diseases Control (CPIDC), University of Texas Health Science Center at Tyler, Tyler, TX, United States of America.
Renuka SubramaniamCenter for Pulmonary and Infectious Diseases Control (CPIDC), University of Texas Health Science Center at Tyler, Tyler, TX, United States of America.
Han ChenCenter for Pulmonary and Infectious Diseases Control (CPIDC), University of Texas Health Science Center at Tyler, Tyler, TX, United States of America.
Anthony SmithCenter for Pulmonary and Infectious Diseases Control (CPIDC), University of Texas Health Science Center at Tyler, Tyler, TX, United States of America.
Shiva KeshavaDepartment of Cellular and Molecular Biology, University of Texas Health Science Center at Tyler, Tyler, TX, United States of America.
Homayoun ShamsCenter for Pulmonary and Infectious Diseases Control (CPIDC), University of Texas Health Science Center at Tyler, Tyler, TX, United States of America.ORCID http://orcid.org/0000-0003-3857-8927
The University of Texas Health Science Center at Tyler · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Efferocytosis by alveolar phagocytes (APs) is pivotal in maintenance of lung homeostasis. Increased efferocytosis by APs results in protection against lethal acute lung injury due to pulmonary infections whereas defective efferocytosis by APs results in chronic lung inflammation. In this report, we show that pulmonary delivery of Bacillus Calmette-Guerin (BCG) significantly enhances efferocytosis by APs. Increased efferocytosis by APs maintains lung homeostasis and protects mice against lethal influenza pneumonia. Intranasally treated wild type C57Bl/6 (WT) mice with BCG showed significant increase in APs efferocytosis in vivo compared to their PBS-treated counterparts. All BCG-treated WT mice survived lethal influenza A virus (IAV) infection whereas all PBS-treated mice succumbed. BCG-induced resistance was abrogated by depleting AP prior to IAV infection. BCG treatment increased uptake, and digestion/removal of apoptotic cells by APs. BCG significantly increased the expression of TIM4 on APs and increased expression of Rab5 and Rab7. We demonstrated that increased efferocytosis by APs through pulmonary delivery of BCG initiated rapid clearance of apoptotic cells from the alveolar space, maintained lung homeostasis, reduced inflammation and protected host against lethal IAV pneumonia.

Indexed as

AnimalsBCG VaccineDisease Models, AnimalHumansInflammationInfluenza A virusInfluenza, HumanLungMacrophages, AlveolarMicePhagocytesPhagocytosisPneumoniaBCG Vaccine

Identifiers

PMID28686604
PMCPMC5501455
OpenAlexW2734190459

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.