Toxoplasma gondii Infection Induces Suppression in a Mouse Model of Allergic Airway Inflammation

Autor: Valentina Martin, Mariana Argenziano, Romina Chiurazzi, Ignacio Martín Fenoy, Mariano Sergio Picchio, Vanesa Roxana Sánchez, Ariadna Soledad Soto, Alejandra Goldman
Rok vydání: 2012
Předmět:
Allergy
Mouse
Protozoology
medicine.disease_cause
Bronchoalveolar Lavage
Toxoplasma Gondii
Mice
Allergen
Transforming Growth Factor beta
Interferon gamma
Immune Response
Mice
Knockout

Mice
Inbred BALB C

Mice
Inbred C3H

Multidisciplinary
biology
T Cells
Allergy and Hypersensitivity
FOXP3
Forkhead Transcription Factors
Animal Models
medicine.anatomical_structure
CD4 Antigens
Medicine
medicine.symptom
Toxoplasma
Toxoplasmosis
Research Article
medicine.drug
Science
Immune Cells
T cell
Immunology
Inflammation
Microbiology
Immunomodulation
Interferon-gamma
Model Organisms
Th2 Cells
Immune system
Hypersensitivity
Respiratory Hypersensitivity
medicine
Animals
Biology
Toxoplasma gondii
Immunologic Subspecialties
biology.organism_classification
medicine.disease
Asthma
Parastic Protozoans
Lymph Nodes
Pulmonary Immunology
Zdroj: PLoS ONE
PLoS ONE, Vol 7, Iss 8, p e43420 (2012)
ISSN: 1932-6203
Popis: Allergic asthma is an inflammatory disorder characterized by infiltration of the airway wall with inflammatory cells driven mostly by activation of Th2-lymphocytes, eosinophils and mast cells. There is a link between increased allergy and a reduction of some infections in Western countries. Epidemiological data also show that respiratory allergy is less frequent in people exposed to orofecal and foodborne microbes such as Toxoplasma gondii. We previously showed that both acute and chronic parasite T. gondii infection substantially blocked development of airway inflammation in adult BALB/c mice. Based on the high levels of IFN-γ along with the reduction of Th2 phenotype, we hypothesized that the protective effect might be related to the strong Th1 immune response elicited against the parasite. However, other mechanisms could also be implicated. The possibility that regulatory T cells inhibit allergic diseases has received growing support from both animal and human studies. Here we investigated the cellular mechanisms involved in T. gondii induced protection against allergy. Our results show for the first time that thoracic lymph node cells from mice sensitized during chronic T. gondii infection have suppressor activity. Suppression was detected both in vitro, on allergen specific T cell proliferation and in vivo, on allergic lung inflammation after adoptive transference from infected/sensitized mice to previously sensitized animals. This ability was found to be contact-independent and correlated with high levels of TGF-β and CD4(+)FoxP3(+) cells.
Databáze: OpenAIRE