Cargando…

Vaccines against leishmaniasis: using controlled human infection models to accelerate development

INTRODUCTION: Leishmaniasis is a neglected tropical disease that is defined by the World Health Organization as vaccine preventable. Although several new candidate vaccines are in development, no vaccine has successfully reached the market for human use. Several species of Leishmania cause human dis...

Descripción completa

Detalles Bibliográficos
Autores principales: Parkash, Vivak, Kaye, Paul M., Layton, Alison M, Lacey, Charles J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835556/
https://www.ncbi.nlm.nih.gov/pubmed/34664543
http://dx.doi.org/10.1080/14760584.2021.1991795
_version_ 1784868692308262912
author Parkash, Vivak
Kaye, Paul M.
Layton, Alison M
Lacey, Charles J
author_facet Parkash, Vivak
Kaye, Paul M.
Layton, Alison M
Lacey, Charles J
author_sort Parkash, Vivak
collection PubMed
description INTRODUCTION: Leishmaniasis is a neglected tropical disease that is defined by the World Health Organization as vaccine preventable. Although several new candidate vaccines are in development, no vaccine has successfully reached the market for human use. Several species of Leishmania cause human disease and have co-evolved with their respective sand fly vectors. These unique relationships have implications for initiation of infection and vaccine development. An approach to vaccine development for many infectious diseases is the use of controlled human infection models (CHIMs). AREAS COVERED: We describe the history and recent development of experimental and deliberate infection using Leishmania in humans and the rationale for developing a new sand fly-initiated CHIM to progress leishmaniasis vaccine development. Examples from other infectious diseases are discussed in the context of the development of a new leishmaniasis CHIM. We also reflect upon the manufacture of the challenge agent, practical considerations, safety, ethics, and regulatory issues. EXPERT OPINION: A new cutaneous Leishmania CHIM is being developed to enable testing of vaccines in the development pipeline. Questions remain about the use of such CHIMs to determine effectiveness of vaccines against visceral leishmaniasis. However, such a CHIM will be invaluable in expediting time to market for vaccines.
format Online
Article
Text
id pubmed-9835556
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-98355562023-01-13 Vaccines against leishmaniasis: using controlled human infection models to accelerate development Parkash, Vivak Kaye, Paul M. Layton, Alison M Lacey, Charles J Expert Rev Vaccines Review INTRODUCTION: Leishmaniasis is a neglected tropical disease that is defined by the World Health Organization as vaccine preventable. Although several new candidate vaccines are in development, no vaccine has successfully reached the market for human use. Several species of Leishmania cause human disease and have co-evolved with their respective sand fly vectors. These unique relationships have implications for initiation of infection and vaccine development. An approach to vaccine development for many infectious diseases is the use of controlled human infection models (CHIMs). AREAS COVERED: We describe the history and recent development of experimental and deliberate infection using Leishmania in humans and the rationale for developing a new sand fly-initiated CHIM to progress leishmaniasis vaccine development. Examples from other infectious diseases are discussed in the context of the development of a new leishmaniasis CHIM. We also reflect upon the manufacture of the challenge agent, practical considerations, safety, ethics, and regulatory issues. EXPERT OPINION: A new cutaneous Leishmania CHIM is being developed to enable testing of vaccines in the development pipeline. Questions remain about the use of such CHIMs to determine effectiveness of vaccines against visceral leishmaniasis. However, such a CHIM will be invaluable in expediting time to market for vaccines. Taylor & Francis 2021-10-27 /pmc/articles/PMC9835556/ /pubmed/34664543 http://dx.doi.org/10.1080/14760584.2021.1991795 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Parkash, Vivak
Kaye, Paul M.
Layton, Alison M
Lacey, Charles J
Vaccines against leishmaniasis: using controlled human infection models to accelerate development
title Vaccines against leishmaniasis: using controlled human infection models to accelerate development
title_full Vaccines against leishmaniasis: using controlled human infection models to accelerate development
title_fullStr Vaccines against leishmaniasis: using controlled human infection models to accelerate development
title_full_unstemmed Vaccines against leishmaniasis: using controlled human infection models to accelerate development
title_short Vaccines against leishmaniasis: using controlled human infection models to accelerate development
title_sort vaccines against leishmaniasis: using controlled human infection models to accelerate development
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835556/
https://www.ncbi.nlm.nih.gov/pubmed/34664543
http://dx.doi.org/10.1080/14760584.2021.1991795
work_keys_str_mv AT parkashvivak vaccinesagainstleishmaniasisusingcontrolledhumaninfectionmodelstoacceleratedevelopment
AT kayepaulm vaccinesagainstleishmaniasisusingcontrolledhumaninfectionmodelstoacceleratedevelopment
AT laytonalisonm vaccinesagainstleishmaniasisusingcontrolledhumaninfectionmodelstoacceleratedevelopment
AT laceycharlesj vaccinesagainstleishmaniasisusingcontrolledhumaninfectionmodelstoacceleratedevelopment