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1                                              Circumsporozoite, a predominant surface protein, is invo
2 nete micronemal proteins chitinase (PgCHT1), circumsporozoite and TRAP-related protein (CTRP), and vo
3 the first microneme protein of the ookinete: circumsporozoite- and TRAP-related protein (CTRP).
4  seasonal booster doses were tested for anti-circumsporozoite antibodies using enzyme-linked immunoso
5 01, 99.7% of children were positive for anti-circumsporozoite antibodies, with a geometric mean titer
6 ozoite antibody titres using a model of anti-circumsporozoite antibody dynamics and the natural acqui
7                                A strong anti-circumsporozoite antibody response to 3 priming doses of
8                  Here, we report on the anti-circumsporozoite antibody response to seasonal RTS,S/AS0
9 n a 0, 8, and 23-week schedule elicited anti-circumsporozoite antibody responses comparable in magnit
10  immunogenic, with trends toward higher anti-circumsporozoite antibody titers in participants protect
11                                      An anti-circumsporozoite antibody titre of 121 EU/mL (98-153) wa
12     We assessed the association between anti-circumsporozoite antibody titres and the magnitude and d
13                                         Anti-circumsporozoite antibody titres are a surrogate of prot
14                                  Waning anti-circumsporozoite antibody titres predict the duration of
15 n the incidence of clinical malaria and anti-circumsporozoite antibody titres using a model of anti-c
16                      RTS,S/AS01-induced anti-circumsporozoite antibody titres were greater in childre
17 s to P. falciparum schizonts and recombinant circumsporozoite antigen, MSP-1(19), MSP-2, AMA-1, and P
18 cles carrying a recombinant Plasmodium vivax circumsporozoite antigen, VMP001, both entrapped in the
19   After initial successful evaluation of the circumsporozoite-based vaccine RTS,S/SBAS2, developed by
20 isplay two epitopes (MAL1 and MAL2) from the circumsporozoite CS proteins of Plasmodium falciparum an
21 WA-1 isolate) or full-length surface protein circumsporozoite (CS) of Plasmodium yoelii (Py).
22 ubcutaneously injected Plasmodium falciparum circumsporozoite (CS) peptides elicited strong parasite-
23 denovirus expressing a major malaria Ag, the circumsporozoite (CS) protein (AdPyCS), was determined u
24                    The Plasmodium falciparum circumsporozoite (CS) protein (CSP) is a major vaccine t
25 ell epitope derived from a Plasmodium yoelii circumsporozoite (CS) protein (referred to as the PyCS-B
26 ke particle containing Plasmodium falciparum circumsporozoite (CS) protein epitopes, was shown to eli
27 dium uses a PEXEL/VTS motif to introduce the circumsporozoite (CS) protein into the hepatocyte cytopl
28                                              Circumsporozoite (CS) protein is a predominant surface a
29                                              Circumsporozoite (CS) protein is the major surface compo
30                                          The circumsporozoite (CS) protein of malaria parasites (Plas
31 ective recombinant adenovirus expressing the circumsporozoite (CS) protein of Plasmodium yoelii (AdPy
32 viruses expressing selected sequences of the circumsporozoite (CS) protein of the human malaria paras
33 are known to target the repeat region of the circumsporozoite (CS) protein on the parasite surface.
34 rozoites of Plasmodium predominantly express circumsporozoite (CS) protein on their surface, which bi
35               Plasmodium sporozoites display circumsporozoite (CS) protein on their surface, which is
36                                          Two circumsporozoite (CS) protein T cell epitopes, previousl
37  response to the Plasmodium berghei malarial circumsporozoite (CS) protein was severely impaired in C
38 echanism and the specific interaction of the circumsporozoite (CS) protein with liver-specific hepara
39                            Native Plasmodium circumsporozoite (CS) protein, translocated by sporozoit
40 arget for malaria vaccine development is the circumsporozoite (CS) protein, which is expressed on the
41 patitis B surface Ag (HBs) and P. falciparum circumsporozoite (CS) protein-among Tanzanian children i
42                    The Plasmodium falciparum circumsporozoite (CS) protein-based pre-erythrocytic sta
43 e focus on improving the immunogenicity of a circumsporozoite (CS) protein-based vaccine.
44 t, we use an adoptive transfer strategy with circumsporozoite (CS) protein-specific transgenic T cell
45 pecific for the repeat region of the surface circumsporozoite (CS) protein.
46 inimal epitopes of the Plasmodium falciparum circumsporozoite (CS) protein.
47 e repeat sequence of the gene coding for the circumsporozoite (CSP) protein from the AF54087 gene.
48 arly induction of functional IL-21-secreting circumsporozoite (CSP)-specific pTfh cells, together wit
49 anti-repeat Abs that reacted with the native circumsporozoite on P. falciparum sporozoites.
50 s had a striking resemblance to the malarial circumsporozoite precipitate (CSP) reaction.
51 ng monoclonal antibody 3E2 which elicits the circumsporozoite precipitate (CSP)-like reaction and pas
52 phocyte epitope on the Plasmodium falciparum circumsporozoite protein (3D7; amino acids 310 to 319 [E
53 in life and subsequent levels of antibody to circumsporozoite protein (a marker of sporozoite-stage r
54                  After immunization, anti-Pf circumsporozoite protein (anti-PfCSP) (isotype and IgG s
55 ) in BALB/c mice required Plasmodium berghei circumsporozoite protein (CS(252-260))-specific memory C
56 denovirus serotype 35 (Ad35) vector encoding circumsporozoite protein (CS) (Ad35.CS), followed by boo
57                                          The circumsporozoite protein (CS) and the sporozoite surface
58                                              Circumsporozoite protein (CS) is the antigenic target fo
59        T-cell responses directed against the circumsporozoite protein (CS) of Plasmodium falciparum c
60  multiple-epitope string ME (ME-TRAP) or the circumsporozoite protein (CS) of Plasmodium falciparum.
61 ed the H-2K(d)-restricted CTL epitope of the circumsporozoite protein (CS) of Plasmodium yoelii betwe
62 onkeys and humans by eliciting antibodies to circumsporozoite protein (CS) that inhibit sporozoite in
63   The sporozoite's surface is covered by the circumsporozoite protein (CS), and its region II-plus ha
64                                          The circumsporozoite protein (CS), one of the major proteins
65       Despite extensive genetic diversity of circumsporozoite protein (CS), the most successful malar
66                                  The malaria circumsporozoite protein (CS), thrombospondin (TSP), and
67                                          The circumsporozoite protein (CS), which covers the surface
68 on the major sporozoite surface protein, the circumsporozoite protein (CS).
69 related adhesion protein (TRAP) 130-138-, or circumsporozoite protein (CSP) 252-260-derived epitopes
70  against the repeat-region of the Plasmodium circumsporozoite protein (CSP) abrogate sporozoite infec
71 gh antibody titers against the P. falciparum circumsporozoite protein (CSP) and a moderate CD4(+) T c
72 rongly against the pre-erythrocytic antigens circumsporozoite protein (CSP) and liver stage antigen 1
73 obulin G (IgG) antibodies to preerythrocytic circumsporozoite protein (CSP) and liver-stage antigen 1
74 ne constructs based on the Plasmodium yoelii circumsporozoite protein (CSP) and P. yoelii merozoite s
75 tested for the presence of antibodies to the circumsporozoite protein (CSP) and the 42-kDa fragment o
76 ticle that presents a designed P. falciparum circumsporozoite protein (CSP) and the Plasmodium vivax
77 rized sporozoite-specific genes encoding the circumsporozoite protein (CSP) and thrombospondin-relate
78 ncies and median levels of IgG antibodies to circumsporozoite protein (CSP) and thrombospondin-relate
79 or clonotypes and recognizing the Pf-derived circumsporozoite protein (CSP) antigen are found in the
80 g the carboxy- and the amino-terminal of the circumsporozoite protein (CSP) antigen without the centr
81 ns a top priority, and vaccines based on the circumsporozoite protein (CSP) are among the lead candid
82                               The Plasmodium circumsporozoite protein (CSP) binds to salivary glands
83                                          The circumsporozoite protein (CSP) builds up the surface coa
84 nduced shedding of the major surface protein circumsporozoite protein (CSP) exposed the SSP3 ectodoma
85               Here, we have investigated the circumsporozoite protein (CSP) for the presence of a GPI
86 d a distinction in the repeat lengths of the circumsporozoite protein (CSP) gene sequences between P.
87 ency correlates positively with both anti-Pf circumsporozoite protein (CSP) IgG and CD8 + CD69+ effec
88  a plasmid expressing Plasmodium yoelii (Py) circumsporozoite protein (CSP) induces H-2Kd-restricted
89 ral repeat of the Plasmodium falciparum (Pf) circumsporozoite protein (CSP) inhibit parasite activity
90                                          The circumsporozoite protein (CSP) is a target for effector
91  The extended rod-like Plasmodium falciparum circumsporozoite protein (CSP) is comprised of three pri
92                    The Plasmodium falciparum circumsporozoite protein (CSP) is critical for sporozoit
93                                          The circumsporozoite protein (CSP) is one of the most studie
94                                          The circumsporozoite protein (CSP) is the major surface prot
95                               The Plasmodium circumsporozoite protein (CSP) is the major surface prot
96                                              Circumsporozoite protein (CSP) is the most abundant prot
97 on the central and C-terminal regions of the circumsporozoite protein (CSP) of P. falciparum.
98 ic recombinant protein, VMP001, based on the circumsporozoite protein (CSP) of P. vivax.
99 t of the FLAG epitope with an epitope of the circumsporozoite protein (CSP) of Plasmodium falciparum
100 nant that displays a B-cell epitope from the circumsporozoite protein (CSP) of Plasmodium falciparum
101                                          The circumsporozoite protein (CSP) of Plasmodium has several
102                                          The circumsporozoite protein (CSP) on the sporozoite surface
103               Plasmodium sporozoites express circumsporozoite protein (CSP) on their surface, an esse
104                                         IL-5 circumsporozoite protein (CSP) ratios, a helper T cell t
105 nd minor repeat of the Plasmodium falciparum circumsporozoite protein (CSP) respectively.
106 omain (Pfs230-Pro) and a short 36-amino acid circumsporozoite protein (CSP) sequence.
107  markers and diversity in the vaccine target circumsporozoite protein (csp) using nanopore sequencing
108                                              Circumsporozoite protein (CSP) variants of P. vivax, bes
109 d vaccinia virus recombinants expressing the circumsporozoite protein (CSP) were evaluated in the Pla
110                      Several epitopes in the circumsporozoite protein (CSP) were identified as target
111 e combines DNA priming against the P. yoelii circumsporozoite protein (CSP) with a subsequent intrave
112                                          The circumsporozoite protein (CSP), a major surface antigen
113 alaria is based on the Plasmodium falciparum circumsporozoite protein (CSP), a major surface protein
114                                              Circumsporozoite protein (CSP), a predominant surface an
115 ein 2 (LISP2), liver-stage antigen 3 (LSA3), circumsporozoite protein (CSP), and a Plasmodium berghei
116 mbospondin-related anonymous protein (TRAP), circumsporozoite protein (CSP), and export protein 1 (Ex
117 RTS,S malaria vaccine, which is based on the circumsporozoite protein (CSP), demonstrated an increase
118 e sporozoites using a combination of surface circumsporozoite protein (CSP), deoxyribonucleic acid, a
119 including apical membrane antigen 1 (AMA-1), circumsporozoite protein (CSP), erythrocyte binding anti
120      The sporozoite's major surface protein, circumsporozoite protein (CSP), is a multifunctional pro
121                                 The P. vivax circumsporozoite protein (CSP), is considered the leadin
122 ch that targets four P. falciparum antigens: circumsporozoite protein (CSP), liver stage antigen 1 (L
123 udy sought to determine if antibodies to the circumsporozoite protein (CSP), liver-stage antigen 1 (L
124                  Levels of IgG antibodies to circumsporozoite protein (CSP), liver-stage antigen type
125 ation of P. falciparum antigens, such as the circumsporozoite protein (CSP), the basis for the RTS, S
126        Antibodies against the NANP repeat of circumsporozoite protein (CSP), the major surface antige
127 n can be prevented by antibodies against the circumsporozoite protein (CSP), the major surface protei
128                                              Circumsporozoite protein (CSP), the most abundant sporoz
129                  Unlike CTL responses to the circumsporozoite protein (CSP), the population of L3-spe
130 he C-terminal region of the vaccine antigen, circumsporozoite protein (CSP), were associated with a r
131 irected against the NANP tetrapeptide of the circumsporozoite protein (CSP), which comprises the vacc
132 e, RTS,S, based on the Plasmodium falciparum circumsporozoite protein (CSP), will likely be the first
133 eading malaria vaccine in development is the circumsporozoite protein (CSP)-based particle vaccine, R
134 inical efficacy of the Plasmodium falciparum circumsporozoite protein (CSP)-based RTS,S/AS01(E) vacci
135 t leading candidate, RTS,S, is a recombinant circumsporozoite protein (CSP)-based vaccine against Pla
136                                              Circumsporozoite protein (CSP)-specific antibody titers,
137     Tetramer staining for the immunodominant circumsporozoite protein (CSP)-specific CD8(+) T cell ep
138 challenge, the RTS,S/AS01B group had greater circumsporozoite protein (CSP)-specific immune responses
139 odium falciparum sporozoite surface antigen, circumsporozoite protein (CSP).
140 ytic malaria antigen, the Plasmodium berghei circumsporozoite protein (CSP).
141 Ag (RESA), and the dominant B epitope of the circumsporozoite protein (CSP).
142 ination with antibody against the Plasmodium circumsporozoite protein (CSP).
143        The most promising antibody target is circumsporozoite protein (CSP).
144  well-characterized vaccine candidate is the circumsporozoite protein (CSP).
145 NPNA repeat and the C-terminal region of the circumsporozoite protein (CSP).
146 ntly based on targeting antigens such as the circumsporozoite protein (CSP).
147 tibodies and CD4(+) T cells specific for the circumsporozoite protein (CSP).
148 bearing the type I repeat region of P. vivax circumsporozoite protein (CSP).
149 es and sulfatide-binding recombinant malaria circumsporozoite protein (MCSP) inhibit this adhesion.
150 istinct regions on the Plasmodium falciparum circumsporozoite protein (PfCSP) and are highly effectiv
151 body CIS43 targets the Plasmodium falciparum circumsporozoite protein (PfCSP) and prevents malaria in
152  Immunization induces 18-fold higher anti-Pf circumsporozoite protein (PfCSP) antibody levels in prot
153  humans, a recombinant Plasmodium falciparum circumsporozoite protein (PfCSP) candidate vaccine, RTS,
154                    The Plasmodium falciparum circumsporozoite protein (PfCSP) is a sporozoite surface
155 on, as well as the C-terminal domain, of the circumsporozoite protein (PfCSP) of the malaria parasite
156 s (mAbs) targeting the Plasmodium falciparum circumsporozoite protein (PfCSP) on sporozoites (SPZ) an
157 t vaccines elicit antibody responses against circumsporozoite protein (PfCSP) that prevent the infect
158 cination was tested for IgG antibodies to Pf circumsporozoite protein (PfCSP) using enzyme-linked imm
159 immunoglobulin G antibodies to P. falciparum circumsporozoite protein (PfCSP) using enzyme-linked imm
160 f proteins, previously described only for Pf circumsporozoite protein (PfCSP), extends to other repea
161 e repeat region of the Plasmodium falciparum circumsporozoite protein (PfCSP), plateaued after two im
162 body responses to Plasmodium falciparum (Pf) circumsporozoite protein (PfCSP), the primary surface an
163  antigens, such as the Plasmodium falciparum circumsporozoite protein (PfCSP), use both sequence dege
164 accine is based on the Plasmodium falciparum circumsporozoite protein (PfCSP), which is O-fucosylated
165 d sequences within the Plasmodium falciparum circumsporozoite protein (PfCSP).
166 ells, specific for the Plasmodium falciparum circumsporozoite protein (PfCSP).
167  response against Plasmodium falciparum (Pf) circumsporozoite protein (PfCSP).
168 ding two preerythrocytic-stage antigens, the circumsporozoite protein (PkCSP) and sporozoite surface
169          The geometric mean anti-P. knowlesi circumsporozoite protein (PkCSP) titers ranged from 1,76
170 DNA plasmid expressing the Plasmodium yoelii circumsporozoite protein (pPyCSP) protects mice against
171 cine which simultaneously expresses P. vivax circumsporozoite protein (PvCSP) and P25 (Pvs25) protein
172 f a pre-erythrocytic vaccine is the P. vivax circumsporozoite protein (PvCSP).
173 studies indicated that the Plasmodium yoelii circumsporozoite protein (PyCSP) 57-70 region elicits T
174 cine plasmids encoding the Plasmodium yoelii circumsporozoite protein (PyCSP) and murine granulocyte-
175 sly shown that a DNA plasmid encoding the Py circumsporozoite protein (PyCSP) can protect mice agains
176 s neonates (7 days) with a Plasmodium yoelii circumsporozoite protein (PyCSP) DNA vaccine mixed with
177                                          The circumsporozoite protein (PyCSP) of Plasmodium yoelii wa
178  CTL responses against the Plasmodium yoelii circumsporozoite protein (PyCSP), BALB/c mice were immun
179 gimen: one inducing high-titer antibodies to circumsporozoite protein (RTS,S/AS01B) and the other ind
180  antigen-175; liver-stage antigen-1 [LSA-1], circumsporozoite protein [CSP], merozoite surface protei
181  The responses to one antigen (P. falciparum circumsporozoite protein [PfCSP]) were similar among vol
182 y against malaria parasites with the matched circumsporozoite protein allele than against mismatched
183 s showed that age-related antibody levels to Circumsporozoite Protein and 10 merozoite proteins incre
184 A recombinant vaccine based on fusion of the circumsporozoite protein and HBsAg plus a potent adjuvan
185 cine comprising nanoparticles, formed from a circumsporozoite protein and hepatitis B surface antigen
186  composed of a fusion protein of the malaria circumsporozoite protein and hepatitis B surface antigen
187 d based on t1/2, the antibody titers against circumsporozoite protein and merozoite surface protein 1
188 investigations of how antibodies bind to the circumsporozoite protein and neutralize sporozoites.
189 r the last dose, antibodies to P. falciparum circumsporozoite protein and PfSPZ were higher in protec
190 iparum antigens derived from the sporozoite (circumsporozoite protein and sporozoite surface protein
191 epitope overlaps a polymorphic region of the circumsporozoite protein and strain cross-reactivity of
192 cell epitopes and sequences derived from the circumsporozoite protein and the merozoite surface prote
193                           All regions of the circumsporozoite protein are targets of functional antib
194 ria and identifies the amino terminus of the circumsporozoite protein as a target of functional antib
195  parasites matched the vaccine in the entire circumsporozoite protein C-terminal (139 infections), as
196 g T3-T1 and a potent B-cell epitope from the circumsporozoite protein central repeat region were test
197 al Asn-Ala-Asn-Pro (NANP) repeat sequence of circumsporozoite protein correlated with vaccine efficac
198 ibody specific for the Plasmodium falciparum circumsporozoite protein expressed on sporozoites.
199 elieved to be responsible for binding to the circumsporozoite protein found on the surface of the Pla
200 he antigen consists of a hybrid in which the circumsporozoite protein fused to hepatitis B surface an
201  positions and haplotypic regions within the circumsporozoite protein had on vaccine efficacy against
202  induced production of IL-2, INF-gamma, anti-circumsporozoite protein IgG, and proliferative T cells.
203 ombinant adenovirus expressing the P. yoelii circumsporozoite protein in mice.
204    Humoral immunity to Plasmodium falciparum circumsporozoite protein is partly mediated by a polymor
205 pecific to certain parasite genotypes at the circumsporozoite protein locus.
206           A plasmid DNA vaccine encoding the circumsporozoite protein of malaria (pCSP) induces toler
207 genetically fused to the minimally truncated circumsporozoite protein of P. falciparum (MCSP) elicits
208 sted with a DNA vaccine plasmid encoding the circumsporozoite protein of P. relictum exhibited a mode
209           The RTS,S/AS01 vaccine targets the circumsporozoite protein of Plasmodium falciparum and ha
210          We developed a vaccine based on the circumsporozoite protein of Plasmodium falciparum that i
211 -4R)-deficient CD8+ T cells specific for the circumsporozoite protein of Plasmodium yoelii develop a
212       Similar results were obtained when the circumsporozoite protein of Plasmodium yoelii was delive
213 hown that a plasmid DNA vaccine encoding the circumsporozoite protein of the malaria parasite elicits
214  high-quality antibody responses against the circumsporozoite protein of the malaria parasite, Plasmo
215 lonal antibodies targeting the P. falciparum circumsporozoite protein on sporozoites, the infective f
216 icted 9-mer epitope of the Plasmodium yoelii circumsporozoite protein or the nucleoprotein of influen
217 ibody responses to the NANP repeat region of circumsporozoite protein peaked after the third dose of
218 region (amino acids 27-117) of P. falciparum circumsporozoite protein plays a critical role in the in
219 rom samples from 4985 participants to survey circumsporozoite protein polymorphisms.
220 derstanding how monoclonal antibodies to the circumsporozoite protein prevent malaria and highlight e
221 optimal dose of an antibody that targets the circumsporozoite protein prior to challenge with P. viva
222               Mice challenged with exogenous circumsporozoite protein produced antibodies against a d
223 h plasmid DNA encoding the plasmodium yoelii circumsporozoite protein protected one of five strains o
224  linear peptide chimeras (LPCs) based on the circumsporozoite protein protects against experimental c
225 accines containing the Plasmodium falciparum Circumsporozoite protein repeat domain are undergoing hu
226 ine containing minimal Plasmodium falciparum circumsporozoite protein repeat epitopes was assessed fo
227 nt P. berghei parasite bearing P. falciparum Circumsporozoite protein repeats.
228               The protective epitopes on the circumsporozoite protein targeted by monoclonal antibodi
229                                          The circumsporozoite protein that covers the surface of Plas
230 B cell epitopes of the Plasmodium falciparum circumsporozoite protein to compare these with previousl
231      Finally, we amplified gene encoding the circumsporozoite protein to determinate their Plasmodium
232          We conclude that the binding of the circumsporozoite protein to hepatic heparan sulfate prot
233 smodium berghei expressing the P. falciparum circumsporozoite protein to mice.
234 n phase 1 study of a full-length recombinant circumsporozoite protein vaccine (rCSP) administered wit
235  have analyzed the DNA sequences of the Csp (circumsporozoite protein) gene in 24 geographically repr
236 with epitopes from the Plasmodium falciparum circumsporozoite protein, also was localized in the tran
237  surface protein of malaria sporozoites, the circumsporozoite protein, binds to heparan sulfate prote
238   The RTS,S/AS01 malaria vaccine targets the circumsporozoite protein, inducing antibodies associated
239   We measured IgG responses to P. falciparum circumsporozoite protein, liver-stage antigen 1, apical-
240   Humoral responses to the malarial antigens circumsporozoite protein, liver-stage antigen-1, apical
241 rasite chitinase, the 25 kDa protein and the circumsporozoite protein, respectively.
242 s against four of the P.falciparum antigens (circumsporozoite protein, sporozoite surface protein 2,
243 te isolated from the whole mosquito binds to circumsporozoite protein, suggesting a role within the m
244 e in the amino terminus of the P. falciparum circumsporozoite protein, the dominant protein on the sp
245 ting that sequences in Plasmodium falciparum circumsporozoite protein, the target antigen in RTS,S/AS
246 s specific for a conserved sequence from the circumsporozoite protein, which binds to many human leuk
247              The most advanced P. falciparum circumsporozoite protein-based malaria vaccine, RTS,S/AS
248 ed, controlled, phase 2b trial, the low-dose circumsporozoite protein-based vaccine R21, with two dif
249     gammadelta T cells were not required for circumsporozoite protein-specific Ab responses, and gamm
250                                              Circumsporozoite protein-specific antibodies correlate p
251                                    baseline) circumsporozoite protein-specific CD4(+) T-cell response
252 of protective CD8(+) T-cell responses to the circumsporozoite protein.
253 zed protective plasmid encoding P. y. yoelii circumsporozoite protein.
254  T cell epitope of the Plasmodium falciparum circumsporozoite protein.
255  coding for the highly polymorphic antigenic circumsporozoite protein.
256  antibody titers targeting the P. falciparum circumsporozoite protein.
257 adenovirus 35 (Ad35) (ARR) vector expressing circumsporozoite protein.
258 l infected hepatocytes that were pulsed with circumsporozoite protein.
259 D of the malaria parasite Plasmodium berghei circumsporozoite protein.
260 g the L. lactis system for the production of circumsporozoite proteins for preclinical and clinical a
261 rotein-1 (PfExp-1), also called antigen 5.1, circumsporozoite related antigen, or QF116.
262                 Here, we describe a model of circumsporozoite-specific memory CD8 T cell generation t
263                      We show that P. berghei circumsporozoite-specific memory CD8 T cells underwent s
264 ell epitopes present in native P. falciparum circumsporozoite surface protein (PfCSP), were fused in
265 a truncated version of Plasmodium falciparum circumsporozoite surface protein (tCSP) fused to Salmone
266                                         Anti-circumsporozoite titres wane according to a biphasic exp
267                         Pre-vaccination anti-circumsporozoite titres were associated with lower immun

 
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