More time to kill: A longer liver stage increases T cell-mediated protection against pre-erythrocytic malaria

被引:2
作者
Yadav, Naveen [1 ,2 ]
Parthiban, Chaitra [1 ,2 ]
Billman, Zachary P. [1 ,2 ]
Stone, Brad C. [1 ,2 ]
Watson, Felicia N. [1 ,2 ]
Zhou, Kevin [1 ,2 ]
Olsen, Tayla M. [1 ,2 ]
Talavera, Irene Cruz [1 ,2 ]
Seilie, Annette Mariko [1 ,2 ]
Kalata, Anya C. [1 ,2 ]
Matsubara, Jokichi [1 ,2 ]
Shears, Melanie J. [1 ,2 ]
Reynolds, Rebekah A. [1 ,2 ]
Murphy, Sean C. [1 ,2 ,3 ]
机构
[1] Univ Washington, Dept Lab Med & Pathol, Seattle, WA 98195 USA
[2] Univ Washington, Ctr Emerging & Reemerging Infect Dis, Seattle, WA 98195 USA
[3] Univ Washington, Dept Microbiol, Seattle, WA 98195 USA
关键词
CIRCUMSPOROZOITE PROTEIN; RESIDENT MEMORY; IMMUNIZATION; SPOROZOITE; IMMUNITY; RESPONSES; MICE; MOUSE; INTERFERON; ANTIBODIES;
D O I
10.1016/j.isci.2023.108489
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Liver stage (LS) Plasmodia mature in 2-2.5 days in rodents compared to 5-6 days in humans. Plasmodium-specific CD8(+) T cell expansion differs across these varied timespans. To mimic the kinetics of CD8(+) T cells of human Plasmodium infection, a two-dose challenge mouse model that achieved 4-5 days of LS antigen exposure was developed. In this model, mice were inoculated with a non-protective, low dose of late-arresting, genetically attenuated sporozoites to initiate T cell activation and then re-inoculated 2- 3 days later with wild-type sporozoites. Vaccines that partially protected against traditional challenge completely protected against two-dose challenge. During the challenge period, CD8(+) T cell frequencies increased in the livers of two-dose challenged mice but not in traditionally challenged mice, further suggesting that this model better recapitulates kinetics of CD8(+) T cell expansion in humans during the P. falciparum LS. Vaccine development and antigen discovery efforts may be aided by using the two-dose challenge strategy.
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页数:19
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