CD8+ T cells from a novel T cell receptor transgenic mouse induce liver-stage immunity that can be boosted by blood-stage infection in rodent malaria.
To follow the fate of CD8+ T cells responsive to Plasmodium berghei ANKA (PbA) infection, we generated an MHC I-restricted TCR transgenic mouse line against this pathogen. T cells from this line, termed PbT-I T cells, were able to respond to blood-stage infection by PbA and two other rodent malaria...
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Public Library of Science (PLoS)
2014
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oai:doaj.org-article:5b78f005829940e1a9169afc90e74c412021-11-18T06:06:33ZCD8+ T cells from a novel T cell receptor transgenic mouse induce liver-stage immunity that can be boosted by blood-stage infection in rodent malaria.1553-73661553-737410.1371/journal.ppat.1004135https://doaj.org/article/5b78f005829940e1a9169afc90e74c412014-05-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24854165/?tool=EBIhttps://doaj.org/toc/1553-7366https://doaj.org/toc/1553-7374To follow the fate of CD8+ T cells responsive to Plasmodium berghei ANKA (PbA) infection, we generated an MHC I-restricted TCR transgenic mouse line against this pathogen. T cells from this line, termed PbT-I T cells, were able to respond to blood-stage infection by PbA and two other rodent malaria species, P. yoelii XNL and P. chabaudi AS. These PbT-I T cells were also able to respond to sporozoites and to protect mice from liver-stage infection. Examination of the requirements for priming after intravenous administration of irradiated sporozoites, an effective vaccination approach, showed that the spleen rather than the liver was the main site of priming and that responses depended on CD8α+ dendritic cells. Importantly, sequential exposure to irradiated sporozoites followed two days later by blood-stage infection led to augmented PbT-I T cell expansion. These findings indicate that PbT-I T cells are a highly versatile tool for studying multiple stages and species of rodent malaria and suggest that cross-stage reactive CD8+ T cells may be utilized in liver-stage vaccine design to enable boosting by blood-stage infections.Lei Shong LauDaniel Fernandez-RuizVanessa MollardAngelika SturmMichelle A NellerAnton CozijnsenJulia L GregoryGayle M DaveyClaerwen M JonesYi-Hsuan LinAshraful HaqueChristian R EngwerdaCatherine Q NieDiana S HansenKenneth M MurphyAnthony T PapenfussJohn J MilesScott R BurrowsTania de Koning-WardGeoffrey I McFaddenFrancis R CarboneBrendan S CrabbWilliam R HeathPublic Library of Science (PLoS)articleImmunologic diseases. AllergyRC581-607Biology (General)QH301-705.5ENPLoS Pathogens, Vol 10, Iss 5, p e1004135 (2014) |
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| topic |
Immunologic diseases. Allergy RC581-607 Biology (General) QH301-705.5 |
| spellingShingle |
Immunologic diseases. Allergy RC581-607 Biology (General) QH301-705.5 Lei Shong Lau Daniel Fernandez-Ruiz Vanessa Mollard Angelika Sturm Michelle A Neller Anton Cozijnsen Julia L Gregory Gayle M Davey Claerwen M Jones Yi-Hsuan Lin Ashraful Haque Christian R Engwerda Catherine Q Nie Diana S Hansen Kenneth M Murphy Anthony T Papenfuss John J Miles Scott R Burrows Tania de Koning-Ward Geoffrey I McFadden Francis R Carbone Brendan S Crabb William R Heath CD8+ T cells from a novel T cell receptor transgenic mouse induce liver-stage immunity that can be boosted by blood-stage infection in rodent malaria. |
| description |
To follow the fate of CD8+ T cells responsive to Plasmodium berghei ANKA (PbA) infection, we generated an MHC I-restricted TCR transgenic mouse line against this pathogen. T cells from this line, termed PbT-I T cells, were able to respond to blood-stage infection by PbA and two other rodent malaria species, P. yoelii XNL and P. chabaudi AS. These PbT-I T cells were also able to respond to sporozoites and to protect mice from liver-stage infection. Examination of the requirements for priming after intravenous administration of irradiated sporozoites, an effective vaccination approach, showed that the spleen rather than the liver was the main site of priming and that responses depended on CD8α+ dendritic cells. Importantly, sequential exposure to irradiated sporozoites followed two days later by blood-stage infection led to augmented PbT-I T cell expansion. These findings indicate that PbT-I T cells are a highly versatile tool for studying multiple stages and species of rodent malaria and suggest that cross-stage reactive CD8+ T cells may be utilized in liver-stage vaccine design to enable boosting by blood-stage infections. |
| format |
article |
| author |
Lei Shong Lau Daniel Fernandez-Ruiz Vanessa Mollard Angelika Sturm Michelle A Neller Anton Cozijnsen Julia L Gregory Gayle M Davey Claerwen M Jones Yi-Hsuan Lin Ashraful Haque Christian R Engwerda Catherine Q Nie Diana S Hansen Kenneth M Murphy Anthony T Papenfuss John J Miles Scott R Burrows Tania de Koning-Ward Geoffrey I McFadden Francis R Carbone Brendan S Crabb William R Heath |
| author_facet |
Lei Shong Lau Daniel Fernandez-Ruiz Vanessa Mollard Angelika Sturm Michelle A Neller Anton Cozijnsen Julia L Gregory Gayle M Davey Claerwen M Jones Yi-Hsuan Lin Ashraful Haque Christian R Engwerda Catherine Q Nie Diana S Hansen Kenneth M Murphy Anthony T Papenfuss John J Miles Scott R Burrows Tania de Koning-Ward Geoffrey I McFadden Francis R Carbone Brendan S Crabb William R Heath |
| author_sort |
Lei Shong Lau |
| title |
CD8+ T cells from a novel T cell receptor transgenic mouse induce liver-stage immunity that can be boosted by blood-stage infection in rodent malaria. |
| title_short |
CD8+ T cells from a novel T cell receptor transgenic mouse induce liver-stage immunity that can be boosted by blood-stage infection in rodent malaria. |
| title_full |
CD8+ T cells from a novel T cell receptor transgenic mouse induce liver-stage immunity that can be boosted by blood-stage infection in rodent malaria. |
| title_fullStr |
CD8+ T cells from a novel T cell receptor transgenic mouse induce liver-stage immunity that can be boosted by blood-stage infection in rodent malaria. |
| title_full_unstemmed |
CD8+ T cells from a novel T cell receptor transgenic mouse induce liver-stage immunity that can be boosted by blood-stage infection in rodent malaria. |
| title_sort |
cd8+ t cells from a novel t cell receptor transgenic mouse induce liver-stage immunity that can be boosted by blood-stage infection in rodent malaria. |
| publisher |
Public Library of Science (PLoS) |
| publishDate |
2014 |
| url |
https://doaj.org/article/5b78f005829940e1a9169afc90e74c41 |
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