Advances in vaccine development for human trichuriasis.

Animal model Trichuris spp trichuriasis vaccine

Journal

Parasitology
ISSN: 1469-8161
Titre abrégé: Parasitology
Pays: England
ID NLM: 0401121

Informations de publication

Date de publication:
24 Mar 2021
Historique:
pubmed: 25 3 2021
medline: 25 3 2021
entrez: 24 3 2021
Statut: aheadofprint

Résumé

Trichuriasis known as whipworm infection caused by Trichuris trichiura, is a highly prevalent soil-transmitted helminthiasis in low- and middle-income countries located in tropical and subtropical areas and affecting approximately 360 million people. Children typically harbour the largest burden of T. trichiura and they are usually co-infected with other soil-transmitted helminth (STH), including Ascaris lumbricoides and hookworm. The consequences of trichuriasis, such as malnutrition and physical and cognitive growth restriction, lead to a massive health burden in endemic regions. Despite the implementation of mass drug administration of anthelminthic treatment to school-age children, T. trichiura infection remains challenging to control due to the low efficacy of current drugs as well as high rates of post-treatment re-infection. Thus, the development of a vaccine that would induce protective immunity and reduce infection rate or community faecal egg output is essential. Hurdles for human whipworm vaccine development include the lack of suitable vaccine antigen targets and animal models for human T. trichiura infection. Instead, rodent whipworm T. muris infected mouse models serve as a major surrogate for testing immunogenicity and efficacy of vaccine candidates. In this review, we summarize recent advances in animal models for T. trichiura antigen discovery and testing of vaccine candidates, while providing an overall view of the current status of T. trichiura vaccine development.

Identifiants

pubmed: 33757603
doi: 10.1017/S0031182021000500
pii: S0031182021000500
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-12

Subventions

Organisme : NIAID NIH HHS
ID : R21 AI144555
Pays : United States

Auteurs

Jesica Hayon (J)

Department of Medicine, Section of Infectious Diseases, Baylor College of Medicine, Houston, TX, USA.

Jill Weatherhead (J)

Department of Medicine, Section of Infectious Diseases, Baylor College of Medicine, Houston, TX, USA.
Department of Pediatrics, Section of Tropical Medicine, Baylor College of Medicine, Houston, TX, USA.
National School of Tropical Medicine, Baylor College of Medicine, Houston, TX, USA.

Peter J Hotez (PJ)

Department of Pediatrics, Section of Tropical Medicine, Baylor College of Medicine, Houston, TX, USA.
National School of Tropical Medicine, Baylor College of Medicine, Houston, TX, USA.
Texas Children's Hospital Center for Vaccine Development, Baylor College of Medicine, Houston, TX77030, USA.

Maria Elena Bottazzi (ME)

Department of Pediatrics, Section of Tropical Medicine, Baylor College of Medicine, Houston, TX, USA.
National School of Tropical Medicine, Baylor College of Medicine, Houston, TX, USA.
Texas Children's Hospital Center for Vaccine Development, Baylor College of Medicine, Houston, TX77030, USA.

Bin Zhan (B)

Department of Pediatrics, Section of Tropical Medicine, Baylor College of Medicine, Houston, TX, USA.
National School of Tropical Medicine, Baylor College of Medicine, Houston, TX, USA.
Texas Children's Hospital Center for Vaccine Development, Baylor College of Medicine, Houston, TX77030, USA.

Classifications MeSH