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  3. Oral Versus Intragastric Inoculation: Similar Pathways of Experimental Infection? From Target Tissues, Parasite Evasion, and Immune Response.
 

Oral Versus Intragastric Inoculation: Similar Pathways of Experimental Infection? From Target Tissues, Parasite Evasion, and Immune Response.

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BORIS DOI
10.7892/boris.124285
Date of Publication
2018
Publication Type
Article
Division/Institute

Theodor-Kocher-Instit...

Author
Barreto de Albuquerque, Julianaorcid-logo
Theodor-Kocher-Institut (TKI)
Silva Dos Santos, Danielle
Stein, Jens Volker
Theodor-Kocher-Institut (TKI)
de Meis, Juliana
Subject(s)

500 - Science::570 - ...

600 - Technology::610...

Series
Frontiers in immunology
ISSN or ISBN (if monograph)
1664-3224
Publisher
Frontiers Research Foundation
Language
English
Publisher DOI
10.3389/fimmu.2018.01734
PubMed ID
30100907
Uncontrolled Keywords

T cell activation Try...

Description
Currently, oral infection is the most frequent transmission mechanism of Chagas disease in Brazil and others Latin American countries. This transmission pathway presents increased mortality rate in the first 2 weeks, which is higher than the calculated mortality after the biting of infected insect vectors. Thus, the oral route of infection, and the consequences in the host must be taken into account when thinking on the mechanisms underlying the natural history of the disease. Distinct routes of parasite entry may differentially affect immune circuits, stimulating regional immune responses that impact on the overall profile of the host protective immunity. Experimental studies related to oral infection usually comprise inoculation in the mouth (oral infection, OI) or gavage (gastrointestinal infection, GI), being often considered as similar routes of infection. Hence, establishing a relationship between the inoculation site (OI or GI) with disease progression and the mounting of -specific regional immune responses is an important issue to be considered. Here, we provide a discussion on studies performed in OI and GI in experimental models of acute infections, including infection.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/62690
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