Evidence map›Paper›PMID 37158369›Full record

ArticleEMBO molecular medicine2023

Subcutaneous BCG vaccination protects against streptococcal pneumonia via regulating innate immune responses in the lung.

Alisha Kang, Gluke Ye, Ramandeep Singh, Sam Afkhami, Jegarubee Bavananthasivam, Xiangqian Luo, Maryam Vaseghi-Shanjani, Fatemah Aleithan, Anna Zganiacz, Mangalakumari Jeyanathan and 1 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 3% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

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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

11 authors at 2 institutions in 2 countries.

Alisha KangMcMaster Immunology Research Centre, M. G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.ORCID 0000-0002-3527-287X
Gluke YeMcMaster Immunology Research Centre, M. G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Ramandeep SinghMcMaster Immunology Research Centre, M. G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Sam AfkhamiMcMaster Immunology Research Centre, M. G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Jegarubee BavananthasivamMcMaster Immunology Research Centre, M. G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Xiangqian LuoDepartment of Pediatric Otolaryngology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Maryam Vaseghi-ShanjaniMcMaster Immunology Research Centre, M. G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Fatemah AleithanMcMaster Immunology Research Centre, M. G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Anna ZganiaczMcMaster Immunology Research Centre, M. G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Mangalakumari JeyanathanMcMaster Immunology Research Centre, M. G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Zhou XingMcMaster Immunology Research Centre, M. G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.ORCID 0000-0001-7856-0663
McMaster University Medical Centre · CASouthern Medical University Shenzhen Hospital · CN

Funding

CIHR
6 · The paper itself

Abstract

Bacillus Calmette-Guérin (BCG) still remains the only licensed vaccine for TB and has been shown to provide nonspecific protection against unrelated pathogens. This has been attributed to the ability of BCG to modulate the innate immune system, known as trained innate immunity (TII). Trained innate immunity is associated with innate immune cells being in a hyperresponsive state leading to enhanced host defense against heterologous infections. Both epidemiological evidence and prospective studies demonstrate cutaneous BCG vaccine-induced TII provides enhanced innate protection against heterologous pathogens. Regardless of the extensive progress made thus far, the effect of cutaneous BCG vaccination against heterologous respiratory bacterial infections and the underlying mechanisms still remain unknown. Here, we show that s.c. BCG vaccine-induced TII provides enhanced heterologous innate protection against pulmonary Streptococcus pneumoniae infection. We further demonstrate that this enhanced innate protection is mediated by enhanced neutrophilia in the lung and is independent of centrally trained circulating monocytes. New insight from this study will help design novel effective vaccination strategies against unrelated respiratory bacterial pathogens.

Indexed as

Mycobacterium bovisPneumoniaBCG VaccineHumansImmunity, InnateLungProspective StudiesVaccinationBCG VaccinelungStreptococcus pneumoniae infectionsubcutaneous BCG vaccinetissue-resident macrophagestrained innate immunity

Identifiers

PMID37158369
PMCPMC10331578
OpenAlexW4375956197

What Socratic 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 Socratic graph.