Evidence map›Paper›PMID 26072063›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2015

Nasal priming with immunobiotic Lactobacillus rhamnosus modulates inflammation-coagulation interactions and reduces influenza virus-associated pulmonary damage.

Hortensia Zelaya, Asuka Tada, Maria Guadalupe Vizoso-Pinto, Susana Salva, Paulraj Kanmani, Graciela Agüero, Susana Alvarez, Haruki Kitazawa, Julio Villena

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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

48 citing papers in PubMed, 72 citations in OpenAlex.

  1. Trial
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  5. CombinedInternational journal of molecular sciences · 2025
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  6. Frontiers in cellular and infection microbiology · 2025
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  7. Orange PeelPharmaceutics · 2024
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  8. Respiratory Delivery ofPharmaceutics · 2024
    Article
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  10. Review
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  13. International journal of molecular sciences · 2023
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  14. The Effect ofMicroorganisms · 2023
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  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

9 authors at 4 institutions in 2 countries.

Hortensia ZelayaImmunobiotics Research Group, Tucumán, Argentina.
Asuka Tada
Maria Guadalupe Vizoso-Pinto
Susana Salva
Paulraj Kanmani
Graciela Agüero
Susana Alvarez
Haruki Kitazawa
Julio Villena
Consejo Nacional de Investigaciones Científicas y Técnicas · ARTohoku University · JPInstituto Superior de Investigaciones Biológicas · ARNational University of Tucumán · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate the effect of the nasal administration of live and heat-killed Lactobacillus rhamnosus CRL1505 (Lr1505) on immune-coagulative response during influenza virus (IFV) infection to improve survival and reduce lung injury.

methodsSix-week-old BALB/c mice were treated with live or heat-killed Lr1505 by the nasal route during two consecutive days. Treated and untreated control mice were then nasally challenged with IFV.

resultsBoth viable and non-viable Lr1505 protected infected mice by reducing pulmonary injury and lung viral loads trough several mechanisms: (a) Inflammatory cytokines were efficiently regulated allowing higher clearance of virus and reduction of inflammatory lung tissue damage, associated to higher levels of the regulatory cytokine IL-10. (b) The antiviral immune response was enhanced with improved levels of type I interferons, CD4(+)IFN-γ(+) lymphocytes, and lung CD11c(+)CD11b(low)CD103(+) and CD11c(+)CD11b(high)CD103(-) dendritic cells. (c) The procoagulant state was reversed mainly by down-regulating tissue factor expression and restoring thrombomodulin levels in lung. The capacity of Lr1505 to improve the outcome of IFV infection would be related to its ability to beneficially modulate lung TLR3-triggered immune response.

conclusionsOur work is the first to demonstrate the ability of an immunobiotic strain to beneficially modulate inflammation-coagulation interactions during IFV infection. Interestingly, non-viable L. rhamnosus CRL1505 was as effective as the viable strain to beneficially modulate respiratory antiviral immune response.

Indexed as

Lacticaseibacillus rhamnosusAcute Lung InjuryAdministration, IntranasalAnimalsBlood CoagulationBronchoalveolar Lavage FluidCytokinesImmunologic FactorsLeukocyte CountLungMaleMice, Inbred BALB COrthomyxoviridaeOrthomyxoviridae InfectionsPlatelet CountPoly I-CCytokinesImmunologic FactorsPoly I-C

Identifiers

PMID26072063
OpenAlexW603441612

What OpenQuestion holds

Textmetadata
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.