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Comprehensive Review of Human Plasmodium falciparum-Specific CD8+T Cell Epitopes
被引:28
作者:
Heide, Janna
[1
,2
]
Vaughan, Kerrie C.
[3
]
Sette, Alessandro
[3
,4
]
Jacobs, Thomas
[5
]
zur Wiesch, Julian Schulze
[1
,2
]
机构:
[1] Univ Med Ctr Hamburg Eppendorf, Dept Med, Infect Dis Unit 1, Hamburg, Germany
[2] German Ctr Infect Res DZIF, Partner Site Hamburg Lubeck Borstel Riems, Hamburg, Germany
[3] La Jolla Inst Immunol, Div Vaccine Discovery, La Jolla, CA USA
[4] Univ Calif San Diego, Dept Med, Div Infect Dis, La Jolla, CA 92093 USA
[5] Bernhard Nocht Inst Trop Med, Protozoa Immunol, Hamburg, Germany
关键词:
malaria;
Plasmodium falciparum;
CD8+;
T cell epitope;
HLA;
restriction;
cytotoxic T cells;
CD8(+) T-CELLS;
ORIGINAL ANTIGENIC SIN;
LIVER-STAGE ANTIGEN-1;
YOELII CIRCUMSPOROZOITE PROTEIN;
GAMMA-INTERFERON RESPONSES;
APICAL MEMBRANE ANTIGEN;
PROTECTIVE IMMUNITY;
MALARIA VACCINE;
BLOOD-STAGE;
LYMPHOCYTE RESPONSES;
D O I:
10.3389/fimmu.2019.00397
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Control of malaria is an important global health issue and there is still an urgent need for the development of an effective prophylactic vaccine. Multiple studies have provided strong evidence that Plasmodium falciparum-specific MHC class I-restricted CD8+ T cells are important for sterile protection against Plasmodium falciparum infection. Here, we present an interactive epitope map of all P. falciparum-specific CD8+ T cell epitopes published to date, based on a comprehensive data base (IEDB), and literature search. The majority of the described P. falciparum-specific CD8+ T cells were directed against the antigens CSP, TRAP, AMA1, and LSA1. Notably, most of the epitopes were discovered in vaccine trials conducted with malaria-naive volunteers. Only few immunological studies of P. falciparum-specific CD8+ T cell epitopes detected in patients suffering from acute malaria or in people living in malaria endemic areas have been published. Further detailed immunological mappings of P. falciparum-specific epitopes of a broader range of P. falciparum proteins in different settings and with different disease status are needed to gain a more comprehensive understanding of the role of CD8+ T cell responses for protection, and to better guide vaccine design and to study their efficacy.
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页数:23
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