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Eosinophil: An innate immune cell with anti‐filarial vaccine and biomarker potential
BACKGROUND: Filarial infections continue to pose a great challenge in endemic countries. One of the central goals in the fight against human filarial infections is the development of strategies that will lead to the inhibition of microfilariae (mf) transmission. Keeping mf under a certain threshold...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240928/ https://www.ncbi.nlm.nih.gov/pubmed/37283884 http://dx.doi.org/10.1002/hsr2.1320 |
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author | Kwarteng, Alexander Mensah, Caleb Osei‐Poku, Priscilla |
author_facet | Kwarteng, Alexander Mensah, Caleb Osei‐Poku, Priscilla |
author_sort | Kwarteng, Alexander |
collection | PubMed |
description | BACKGROUND: Filarial infections continue to pose a great challenge in endemic countries. One of the central goals in the fight against human filarial infections is the development of strategies that will lead to the inhibition of microfilariae (mf) transmission. Keeping mf under a certain threshold within endemic populations will stop transmission and eliminate the infection. METHOD: A narrative review was carried out to identify the possibilities and limitations of exploring the use of eosinophil responses as an anti‐filarial vaccine, and biomarker for the detection of filarial infections. An extensive literature search was performed in online scientific databases including PubMed Central, PubMed, BioMed Central, with the use of predefined search terms. RESULTS: A better understanding of the parasite‐host interactions will lead to the development of improved and better treatment or vaccine strategies that could eliminate filariasis as soon as possible. Highlighted in this review is the explorative use of eosinophil‐producing CLC/Galectin‐10 as a potential biomarker for filarial infections. Also discussed are some genes, and pathways involved in eosinophil recruitments that could be explored for anti‐filarial vaccine development. CONCLUSION: In this short communication, we discuss how eosinophil‐regulated genes, pathways, and networks could be critical in providing more information on how reliably a front‐line immune player could be exploited for anti‐filarial vaccine development and early infection biomarker. |
format | Online Article Text |
id | pubmed-10240928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102409282023-06-06 Eosinophil: An innate immune cell with anti‐filarial vaccine and biomarker potential Kwarteng, Alexander Mensah, Caleb Osei‐Poku, Priscilla Health Sci Rep Narrative Review BACKGROUND: Filarial infections continue to pose a great challenge in endemic countries. One of the central goals in the fight against human filarial infections is the development of strategies that will lead to the inhibition of microfilariae (mf) transmission. Keeping mf under a certain threshold within endemic populations will stop transmission and eliminate the infection. METHOD: A narrative review was carried out to identify the possibilities and limitations of exploring the use of eosinophil responses as an anti‐filarial vaccine, and biomarker for the detection of filarial infections. An extensive literature search was performed in online scientific databases including PubMed Central, PubMed, BioMed Central, with the use of predefined search terms. RESULTS: A better understanding of the parasite‐host interactions will lead to the development of improved and better treatment or vaccine strategies that could eliminate filariasis as soon as possible. Highlighted in this review is the explorative use of eosinophil‐producing CLC/Galectin‐10 as a potential biomarker for filarial infections. Also discussed are some genes, and pathways involved in eosinophil recruitments that could be explored for anti‐filarial vaccine development. CONCLUSION: In this short communication, we discuss how eosinophil‐regulated genes, pathways, and networks could be critical in providing more information on how reliably a front‐line immune player could be exploited for anti‐filarial vaccine development and early infection biomarker. John Wiley and Sons Inc. 2023-06-05 /pmc/articles/PMC10240928/ /pubmed/37283884 http://dx.doi.org/10.1002/hsr2.1320 Text en © 2023 The Authors. Health Science Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Narrative Review Kwarteng, Alexander Mensah, Caleb Osei‐Poku, Priscilla Eosinophil: An innate immune cell with anti‐filarial vaccine and biomarker potential |
title | Eosinophil: An innate immune cell with anti‐filarial vaccine and biomarker potential |
title_full | Eosinophil: An innate immune cell with anti‐filarial vaccine and biomarker potential |
title_fullStr | Eosinophil: An innate immune cell with anti‐filarial vaccine and biomarker potential |
title_full_unstemmed | Eosinophil: An innate immune cell with anti‐filarial vaccine and biomarker potential |
title_short | Eosinophil: An innate immune cell with anti‐filarial vaccine and biomarker potential |
title_sort | eosinophil: an innate immune cell with anti‐filarial vaccine and biomarker potential |
topic | Narrative Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240928/ https://www.ncbi.nlm.nih.gov/pubmed/37283884 http://dx.doi.org/10.1002/hsr2.1320 |
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