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2 nete micronemal proteins chitinase (PgCHT1), circumsporozoite and TRAP-related protein (CTRP), and vo
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
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
12 We assessed the association between anti-circumsporozoite antibody titres and the magnitude and d
15 n the incidence of clinical malaria and anti-circumsporozoite antibody titres using a model of anti-c
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
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
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
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
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
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
44 t, we use an adoptive transfer strategy with circumsporozoite (CS) protein-specific transgenic T cell
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
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
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
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
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
84 nduced shedding of the major surface protein circumsporozoite protein (CSP) exposed the SSP3 ectodoma
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
91 The extended rod-like Plasmodium falciparum circumsporozoite protein (CSP) is comprised of three pri
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
107 markers and diversity in the vaccine target circumsporozoite protein (csp) using nanopore sequencing
109 d vaccinia virus recombinants expressing the circumsporozoite protein (CSP) were evaluated in the Pla
111 e combines DNA priming against the P. yoelii circumsporozoite protein (CSP) with a subsequent intrave
113 alaria is based on the Plasmodium falciparum circumsporozoite protein (CSP), a major surface protein
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
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
125 ation of P. falciparum antigens, such as the circumsporozoite protein (CSP), the basis for the RTS, S
127 n can be prevented by antibodies against the circumsporozoite protein (CSP), the major surface protei
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
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
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,
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
168 ding two preerythrocytic-stage antigens, the circumsporozoite protein (PkCSP) and sporozoite surface
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
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
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
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
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.
204 Humoral immunity to Plasmodium falciparum circumsporozoite protein is partly mediated by a polymor
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
211 -4R)-deficient CD8+ T cells specific for the circumsporozoite protein of Plasmodium yoelii develop a
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
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
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
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
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
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
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
260 g the L. lactis system for the production of circumsporozoite proteins for preclinical and clinical a
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