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1 ation exposes the host to antigens from both preerythrocytic and blood stages, and induced immunity m
2 ect protective biological effects induced by preerythrocytic and/or blood-stage candidate vaccines if
3 ing significant efficacy when expressing the preerythrocytic antigen insert multiple epitope-thrombos
5 date subunit malaria vaccines expressing six preerythrocytic antigens linked together to produce a 32
7 h-level immunoglobulin G (IgG) antibodies to preerythrocytic circumsporozoite protein (CSP) and liver
8 se data introduce a new target of protective preerythrocytic immune responses, PyHEP 17 and its P. fa
10 impanzee adenovirus 63 (ChAd63) encoding the preerythrocytic insert multiple epitope thrombospondin-r
11 two; all vaccines express parts of the same preerythrocytic malaria antigen, the Plasmodium berghei
12 esence of adaptive cell-mediated immunity to preerythrocytic malaria antigens in volunteers from Mali
13 of an early immune response directed against preerythrocytic malaria parasites that are required for
18 ith unstable transmission, IgG antibodies to preerythrocytic P. falciparum antigens vary in subjects
19 t of early immunity directed against malaria preerythrocytic parasites and suggest that gammadelta T
20 ng vaccine classes currently in development: preerythrocytic (PEV), blood stage (BSV), and transmissi
21 (IgG) antibodies to three vaccine candidate preerythrocytic Plasmodium falciparum antigens were eval
22 a should facilitate our understanding of the preerythrocytic Plasmodium life cycle stages and the dev
23 ritical effector cells in protection against preerythrocytic stage malaria, including the potent prot
26 ia species Plasmodium knowlesi including two preerythrocytic-stage antigens, the circumsporozoite pro
29 with a mixture of DNA plasmids encoding two preerythrocytic-stage proteins and two erythrocytic-stag
30 at ChAd63 and MVA expressing PvTRAP are good preerythrocytic-stage vaccine candidates with potential
32 We then evaluated the effect of HIV PIs on preerythrocytic stages in vivo using the rodent parasite
35 at CD8(+) T cells play in protection against preerythrocytic stages of malaria; however, there is mou
40 have been widely used to assess efficacy of preerythrocytic vaccine candidates in small proof-of-con
41 protein, FMP011, has been manufactured as a preerythrocytic vaccine to induce an immune response tha
42 ite vaccine, the "gold standard" for malaria preerythrocytic vaccines, was sporozoite-neutralizing an
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