Nasal priming with immunobiotic Lactobacillus rhamnosus modulates inflammation–coagulation interactions and reduces influenza virus-associated pulmonary damage
Male
Acute Lung Injury
COAGULATION
Leukocyte Count
03 medical and health sciences
INFLAMMATION
Orthomyxoviridae Infections
https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/3.1
https://purl.org/becyt/ford/3.2
Animals
Immunologic Factors
https://purl.org/becyt/ford/3
TLR3
https://purl.org/becyt/ford/1
Blood Coagulation
Lung
Administration, Intranasal
Mice, Inbred BALB C
0303 health sciences
Lacticaseibacillus rhamnosus
Platelet Count
Probiotics
LACTOBACILLUS RHAMNOSUS CRL1505
POLY(I:C)
Orthomyxoviridae
3. Good health
Poly I-C
Cytokines
INFLUENZA VIRUS
Bronchoalveolar Lavage Fluid
DOI:
10.1007/s00011-015-0837-6
Publication Date:
2015-06-13T01:01:40Z
AUTHORS (9)
ABSTRACT
To 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.Six-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.Both 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.Our 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.
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