Comparative assessment of transmission-blocking vaccine candidates against Plasmodium falciparum

Research output: Contribution to journal › Journal article › Research › peer-review

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Comparative assessment of transmission-blocking vaccine candidates against Plasmodium falciparum. / Kapulu, M C; Da, D F; Miura, K; Li, Y; Blagborough, A M; Churcher, T S; Nikolaeva, D; Williams, Andrew Richard; Goodman, A L; Sangare, I; Turner, A V; Cottingham, M G; Nicosia, A; Straschil, U; Tsuboi, T; Gilbert, S C; Long, Carole A; Sinden, R E; Draper, S J; Hill, A V S; Cohuet, A; Biswas, S.

In: Scientific Reports, Vol. 5, 11193, 2015.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Kapulu, MC, Da, DF, Miura, K, Li, Y, Blagborough, AM, Churcher, TS, Nikolaeva, D, Williams, AR, Goodman, AL, Sangare, I, Turner, AV, Cottingham, MG, Nicosia, A, Straschil, U, Tsuboi, T, Gilbert, SC, Long, CA, Sinden, RE, Draper, SJ, Hill, AVS, Cohuet, A & Biswas, S 2015, 'Comparative assessment of transmission-blocking vaccine candidates against Plasmodium falciparum', Scientific Reports, vol. 5, 11193. https://doi.org/10.1038/srep11193

APA

Kapulu, M. C., Da, D. F., Miura, K., Li, Y., Blagborough, A. M., Churcher, T. S., Nikolaeva, D., Williams, A. R., Goodman, A. L., Sangare, I., Turner, A. V., Cottingham, M. G., Nicosia, A., Straschil, U., Tsuboi, T., Gilbert, S. C., Long, C. A., Sinden, R. E., Draper, S. J., ... Biswas, S. (2015). Comparative assessment of transmission-blocking vaccine candidates against Plasmodium falciparum. Scientific Reports, 5, [11193]. https://doi.org/10.1038/srep11193

Vancouver

Kapulu MC, Da DF, Miura K, Li Y, Blagborough AM, Churcher TS et al. Comparative assessment of transmission-blocking vaccine candidates against Plasmodium falciparum. Scientific Reports. 2015;5. 11193. https://doi.org/10.1038/srep11193

Author

Kapulu, M C ; Da, D F ; Miura, K ; Li, Y ; Blagborough, A M ; Churcher, T S ; Nikolaeva, D ; Williams, Andrew Richard ; Goodman, A L ; Sangare, I ; Turner, A V ; Cottingham, M G ; Nicosia, A ; Straschil, U ; Tsuboi, T ; Gilbert, S C ; Long, Carole A ; Sinden, R E ; Draper, S J ; Hill, A V S ; Cohuet, A ; Biswas, S. / Comparative assessment of transmission-blocking vaccine candidates against Plasmodium falciparum. In: Scientific Reports. 2015 ; Vol. 5.

Bibtex

@article{82845a43f3b94866acd7f02d7f3e3b08,
title = "Comparative assessment of transmission-blocking vaccine candidates against Plasmodium falciparum",
abstract = "Malaria transmission-blocking vaccines (TBVs) target the development of Plasmodium parasites within the mosquito, with the aim of preventing malaria transmission from one infected individual to another. Different vaccine platforms, mainly protein-in-adjuvant formulations delivering the leading candidate antigens, have been developed independently and have reported varied transmission-blocking activities (TBA). Here, recombinant chimpanzee adenovirus 63, ChAd63, and modified vaccinia virus Ankara, MVA, expressing AgAPN1, Pfs230-C, Pfs25, and Pfs48/45 were generated. Antibody responses primed individually against all antigens by ChAd63 immunization in BALB/c mice were boosted by the administration of MVA expressing the same antigen. These antibodies exhibited a hierarchy of inhibitory activity against the NF54 laboratory strain of P. falciparum in Anopheles stephensi mosquitoes using the standard membrane feeding assay (SMFA), with anti-Pfs230-C and anti-Pfs25 antibodies giving complete blockade. The observed rank order of inhibition was replicated against P. falciparum African field isolates in A. gambiae in direct membrane feeding assays (DMFA). TBA achieved was IgG concentration dependent. This study provides the first head-to-head comparative analysis of leading antigens using two different parasite sources in two different vector species, and can be used to guide selection of TBVs for future clinical development using the viral-vectored delivery platform.",
author = "Kapulu, {M C} and Da, {D F} and K Miura and Y Li and Blagborough, {A M} and Churcher, {T S} and D Nikolaeva and Williams, {Andrew Richard} and Goodman, {A L} and I Sangare and Turner, {A V} and Cottingham, {M G} and A Nicosia and U Straschil and T Tsuboi and Gilbert, {S C} and Long, {Carole A} and Sinden, {R E} and Draper, {S J} and Hill, {A V S} and A Cohuet and S Biswas",
year = "2015",
doi = "10.1038/srep11193",
language = "English",
volume = "5",
journal = "Scientific Reports",
issn = "2045-2322",
publisher = "nature publishing group",

}

RIS

TY - JOUR

T1 - Comparative assessment of transmission-blocking vaccine candidates against Plasmodium falciparum

AU - Kapulu, M C

AU - Da, D F

AU - Miura, K

AU - Li, Y

AU - Blagborough, A M

AU - Churcher, T S

AU - Nikolaeva, D

AU - Williams, Andrew Richard

AU - Goodman, A L

AU - Sangare, I

AU - Turner, A V

AU - Cottingham, M G

AU - Nicosia, A

AU - Straschil, U

AU - Tsuboi, T

AU - Gilbert, S C

AU - Long, Carole A

AU - Sinden, R E

AU - Draper, S J

AU - Hill, A V S

AU - Cohuet, A

AU - Biswas, S

PY - 2015

Y1 - 2015

N2 - Malaria transmission-blocking vaccines (TBVs) target the development of Plasmodium parasites within the mosquito, with the aim of preventing malaria transmission from one infected individual to another. Different vaccine platforms, mainly protein-in-adjuvant formulations delivering the leading candidate antigens, have been developed independently and have reported varied transmission-blocking activities (TBA). Here, recombinant chimpanzee adenovirus 63, ChAd63, and modified vaccinia virus Ankara, MVA, expressing AgAPN1, Pfs230-C, Pfs25, and Pfs48/45 were generated. Antibody responses primed individually against all antigens by ChAd63 immunization in BALB/c mice were boosted by the administration of MVA expressing the same antigen. These antibodies exhibited a hierarchy of inhibitory activity against the NF54 laboratory strain of P. falciparum in Anopheles stephensi mosquitoes using the standard membrane feeding assay (SMFA), with anti-Pfs230-C and anti-Pfs25 antibodies giving complete blockade. The observed rank order of inhibition was replicated against P. falciparum African field isolates in A. gambiae in direct membrane feeding assays (DMFA). TBA achieved was IgG concentration dependent. This study provides the first head-to-head comparative analysis of leading antigens using two different parasite sources in two different vector species, and can be used to guide selection of TBVs for future clinical development using the viral-vectored delivery platform.

AB - Malaria transmission-blocking vaccines (TBVs) target the development of Plasmodium parasites within the mosquito, with the aim of preventing malaria transmission from one infected individual to another. Different vaccine platforms, mainly protein-in-adjuvant formulations delivering the leading candidate antigens, have been developed independently and have reported varied transmission-blocking activities (TBA). Here, recombinant chimpanzee adenovirus 63, ChAd63, and modified vaccinia virus Ankara, MVA, expressing AgAPN1, Pfs230-C, Pfs25, and Pfs48/45 were generated. Antibody responses primed individually against all antigens by ChAd63 immunization in BALB/c mice were boosted by the administration of MVA expressing the same antigen. These antibodies exhibited a hierarchy of inhibitory activity against the NF54 laboratory strain of P. falciparum in Anopheles stephensi mosquitoes using the standard membrane feeding assay (SMFA), with anti-Pfs230-C and anti-Pfs25 antibodies giving complete blockade. The observed rank order of inhibition was replicated against P. falciparum African field isolates in A. gambiae in direct membrane feeding assays (DMFA). TBA achieved was IgG concentration dependent. This study provides the first head-to-head comparative analysis of leading antigens using two different parasite sources in two different vector species, and can be used to guide selection of TBVs for future clinical development using the viral-vectored delivery platform.

U2 - 10.1038/srep11193

DO - 10.1038/srep11193

M3 - Journal article

C2 - 26063320

VL - 5

JO - Scientific Reports

JF - Scientific Reports

SN - 2045-2322

M1 - 11193

ER -

ID: 139032106