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Adjuvant-free immunization with infective filarial larvae as lymphatic homing antigen carriers
Controlled infection with intestinal nematodes has therapeutic potential for preventing the symptoms of allergic and autoimmune diseases. Here, we engineered larvae of the filarial nematode Litomosoides sigmodontis as a vaccine strategy to induce adaptive immunity against a foreign, crosslinked prot...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6978462/ https://www.ncbi.nlm.nih.gov/pubmed/31974398 http://dx.doi.org/10.1038/s41598-020-57995-8 |
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author | Card, Catherine Wilson, David S. Hirosue, Sachiko Rincon-Restrepo, Marcela de Titta, Alexandre Güç, Esra Martin, Coralie Bain, Odile Swartz, Melody A. Kilarski, Witold W. |
author_facet | Card, Catherine Wilson, David S. Hirosue, Sachiko Rincon-Restrepo, Marcela de Titta, Alexandre Güç, Esra Martin, Coralie Bain, Odile Swartz, Melody A. Kilarski, Witold W. |
author_sort | Card, Catherine |
collection | PubMed |
description | Controlled infection with intestinal nematodes has therapeutic potential for preventing the symptoms of allergic and autoimmune diseases. Here, we engineered larvae of the filarial nematode Litomosoides sigmodontis as a vaccine strategy to induce adaptive immunity against a foreign, crosslinked protein, chicken egg ovalbumin (OVA), in the absence of an external adjuvant. The acylation of filarial proteins with fluorescent probes or biotin was not immediately detrimental to larval movement and survival, which died 3 to 5 days later. At least some of the labeled and skin-inoculated filariae migrated through lymphatic vessels to draining lymph nodes. The immunization potential of OVA-biotin-filariae was compared to that of an OVA-bound nanoparticulate carrier co-delivered with a CpG adjuvant in a typical vaccination scheme. Production of IFNγ and TNFα by restimulated CD4+ cells but not CD8+ confirmed the specific ability of filariae to stimulate CD4(+) T cells. This alternative method of immunization exploits the intrinsic adjuvancy of the attenuated nematode carrier and has the potential to shift the vaccination immune response towards cellular immunity. |
format | Online Article Text |
id | pubmed-6978462 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69784622020-01-30 Adjuvant-free immunization with infective filarial larvae as lymphatic homing antigen carriers Card, Catherine Wilson, David S. Hirosue, Sachiko Rincon-Restrepo, Marcela de Titta, Alexandre Güç, Esra Martin, Coralie Bain, Odile Swartz, Melody A. Kilarski, Witold W. Sci Rep Article Controlled infection with intestinal nematodes has therapeutic potential for preventing the symptoms of allergic and autoimmune diseases. Here, we engineered larvae of the filarial nematode Litomosoides sigmodontis as a vaccine strategy to induce adaptive immunity against a foreign, crosslinked protein, chicken egg ovalbumin (OVA), in the absence of an external adjuvant. The acylation of filarial proteins with fluorescent probes or biotin was not immediately detrimental to larval movement and survival, which died 3 to 5 days later. At least some of the labeled and skin-inoculated filariae migrated through lymphatic vessels to draining lymph nodes. The immunization potential of OVA-biotin-filariae was compared to that of an OVA-bound nanoparticulate carrier co-delivered with a CpG adjuvant in a typical vaccination scheme. Production of IFNγ and TNFα by restimulated CD4+ cells but not CD8+ confirmed the specific ability of filariae to stimulate CD4(+) T cells. This alternative method of immunization exploits the intrinsic adjuvancy of the attenuated nematode carrier and has the potential to shift the vaccination immune response towards cellular immunity. Nature Publishing Group UK 2020-01-23 /pmc/articles/PMC6978462/ /pubmed/31974398 http://dx.doi.org/10.1038/s41598-020-57995-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Card, Catherine Wilson, David S. Hirosue, Sachiko Rincon-Restrepo, Marcela de Titta, Alexandre Güç, Esra Martin, Coralie Bain, Odile Swartz, Melody A. Kilarski, Witold W. Adjuvant-free immunization with infective filarial larvae as lymphatic homing antigen carriers |
title | Adjuvant-free immunization with infective filarial larvae as lymphatic homing antigen carriers |
title_full | Adjuvant-free immunization with infective filarial larvae as lymphatic homing antigen carriers |
title_fullStr | Adjuvant-free immunization with infective filarial larvae as lymphatic homing antigen carriers |
title_full_unstemmed | Adjuvant-free immunization with infective filarial larvae as lymphatic homing antigen carriers |
title_short | Adjuvant-free immunization with infective filarial larvae as lymphatic homing antigen carriers |
title_sort | adjuvant-free immunization with infective filarial larvae as lymphatic homing antigen carriers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6978462/ https://www.ncbi.nlm.nih.gov/pubmed/31974398 http://dx.doi.org/10.1038/s41598-020-57995-8 |
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