Multi-Dose Priming Regimens of PfSPZ Vaccine: Safety and Efficacy against Controlled Human Malaria Infection in Equatoguinean Adults

Plasmodium falciparum sporozoite (PfSPZ) Vaccine is composed of radiation-attenuated, aseptic, purified cryopreserved PfSPZ. Multiple clinical trials empirically assessing two to six doses have shown multi-dose priming (two to four doses the first week) to be optimal for protection in both 4- and 16...

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Veröffentlicht in:The American journal of tropical medicine and hygiene 2022-04, Vol.106 (4), p.1215-1226
Hauptverfasser: Jongo, Said Abdallah, Church, L W Preston, Nchama, Vicente Urbano Nsue Ndong, Hamad, Ali, Chuquiyauri, Raul, Kassim, Kamaka Ramadhani, Athuman, Thabit, Deal, Anna, Natasha, K C, Mtoro, Ali, Mpina, Maxmillian, Nyakarungu, Elizabeth, Bidjimi, Gertrudis Owono, Owono, Marta Alene, Mayé, Escolástica Raquel Mansogo, Mangue, Martín Eká Ondó, Okomo, Genaro Nsué Nguema, Pasialo, Beltrán Ekuá Ntutumu, Mandumbi, Dolores Mbang Ondó, Mikue, María-Silvia A López, Mochomuemue, Fortunata Lobede, Obono, Mariano Obiang, Besahá, Juan Carlos Momo, Bijeri, José Raso, Abegue, Gabriel Mbá, Veri, Yolanda Rimoy, Bela, Ines Toichoa, Chochi, Federico Comsil, Lima Sánchez, José Enrique, Pencelli, Vanessa, Gayozo, Griselda, Nlang, José Antonio Esono Mbá, Schindler, Tobias, James, Eric R, Abebe, Yonas, Lemiale, Laurence, Stabler, Thomas C, Murshedkar, Tooba, Chen, Mei-Chun, Schwabe, Christopher, Ratsirarson, Josea, Rivas, Matilde Riloha, Ayekaba, Mitoha Ondo'o, Milang, Diosdado Vicente Nsué, Falla, Carlos Cortés, Phiri, Wonder P, García, Guillermo A, Maas, Carl D, Nlavo, Bonifacio Manguire, Tanner, Marcel, Billingsley, Peter F, Kim Lee Sim, B, Daubenberger, Claudia, Hoffman, Stephen L, Abdulla, Salim, Richie, Thomas L
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container_issue 4
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container_title The American journal of tropical medicine and hygiene
container_volume 106
creator Jongo, Said Abdallah
Church, L W Preston
Nchama, Vicente Urbano Nsue Ndong
Hamad, Ali
Chuquiyauri, Raul
Kassim, Kamaka Ramadhani
Athuman, Thabit
Deal, Anna
Natasha, K C
Mtoro, Ali
Mpina, Maxmillian
Nyakarungu, Elizabeth
Bidjimi, Gertrudis Owono
Owono, Marta Alene
Mayé, Escolástica Raquel Mansogo
Mangue, Martín Eká Ondó
Okomo, Genaro Nsué Nguema
Pasialo, Beltrán Ekuá Ntutumu
Mandumbi, Dolores Mbang Ondó
Mikue, María-Silvia A López
Mochomuemue, Fortunata Lobede
Obono, Mariano Obiang
Besahá, Juan Carlos Momo
Bijeri, José Raso
Abegue, Gabriel Mbá
Veri, Yolanda Rimoy
Bela, Ines Toichoa
Chochi, Federico Comsil
Lima Sánchez, José Enrique
Pencelli, Vanessa
Gayozo, Griselda
Nlang, José Antonio Esono Mbá
Schindler, Tobias
James, Eric R
Abebe, Yonas
Lemiale, Laurence
Stabler, Thomas C
Murshedkar, Tooba
Chen, Mei-Chun
Schwabe, Christopher
Ratsirarson, Josea
Rivas, Matilde Riloha
Ayekaba, Mitoha Ondo'o
Milang, Diosdado Vicente Nsué
Falla, Carlos Cortés
Phiri, Wonder P
García, Guillermo A
Maas, Carl D
Nlavo, Bonifacio Manguire
Tanner, Marcel
Billingsley, Peter F
Kim Lee Sim, B
Daubenberger, Claudia
Hoffman, Stephen L
Abdulla, Salim
Richie, Thomas L
description Plasmodium falciparum sporozoite (PfSPZ) Vaccine is composed of radiation-attenuated, aseptic, purified cryopreserved PfSPZ. Multiple clinical trials empirically assessing two to six doses have shown multi-dose priming (two to four doses the first week) to be optimal for protection in both 4- and 16-week regimens. In this randomized, double-blind, normal saline (NS) placebo-controlled trial, four groups (G) of 18- to 32-year-old Equatoguineans received multi-dose priming regimens with or without a delayed final dose at 4 or 16 weeks. The regimens were G1: days 1, 3, 5, 7, and 113; G2: days 1, 3, 5, and 7; G3: days 1, 3, 5, 7, and 29; and G4: days 1, 8, and 29. All doses were 9 × 105 PfSPZ. Tolerability, safety, immunogenicity, and vaccine efficacy (VE) against homologous controlled human malaria infection (CHMI) 6-7 weeks after vaccination were assessed to down-select the best regimen. All four regimens were safe and well tolerated, with no significant differences in adverse events (AEs) between vaccinees (N = 84) and NS controls (N = 20) or between regimens. Out of 19 controls, 13 developed Pf parasitemia by quantitative polymerase chain reaction (qPCR) after CHMI. Only the vaccine regimen administered on study days 1, 8, and 29 gave significant protection (7/21 vaccinees versus 13/19 controls infected, VE 51.3%, P = 0.03, Barnard's test, two-tailed). There were no significant differences in antibodies against Pf circumsporozoite protein (PfCSP), a major SPZ antigen, between protected and nonprotected vaccinees or controls pre-CHMI. The six controls not developing Pf parasitemia had significantly higher antibodies to blood stage antigens Pf exported protein 1 (PfEXP1) and Pf merozoite surface protein 1 (PfMSP1) than the controls who developed parasitemia, suggesting naturally acquired immunity against Pf limited infections in controls. This study identified a safe, protective, 4-week, multi-dose prime vaccination regimen for assessment in future trials of PfSPZ Vaccine.
doi_str_mv 10.4269/ajtmh.21-0942
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Multiple clinical trials empirically assessing two to six doses have shown multi-dose priming (two to four doses the first week) to be optimal for protection in both 4- and 16-week regimens. In this randomized, double-blind, normal saline (NS) placebo-controlled trial, four groups (G) of 18- to 32-year-old Equatoguineans received multi-dose priming regimens with or without a delayed final dose at 4 or 16 weeks. The regimens were G1: days 1, 3, 5, 7, and 113; G2: days 1, 3, 5, and 7; G3: days 1, 3, 5, 7, and 29; and G4: days 1, 8, and 29. All doses were 9 × 105 PfSPZ. Tolerability, safety, immunogenicity, and vaccine efficacy (VE) against homologous controlled human malaria infection (CHMI) 6-7 weeks after vaccination were assessed to down-select the best regimen. All four regimens were safe and well tolerated, with no significant differences in adverse events (AEs) between vaccinees (N = 84) and NS controls (N = 20) or between regimens. Out of 19 controls, 13 developed Pf parasitemia by quantitative polymerase chain reaction (qPCR) after CHMI. Only the vaccine regimen administered on study days 1, 8, and 29 gave significant protection (7/21 vaccinees versus 13/19 controls infected, VE 51.3%, P = 0.03, Barnard's test, two-tailed). There were no significant differences in antibodies against Pf circumsporozoite protein (PfCSP), a major SPZ antigen, between protected and nonprotected vaccinees or controls pre-CHMI. The six controls not developing Pf parasitemia had significantly higher antibodies to blood stage antigens Pf exported protein 1 (PfEXP1) and Pf merozoite surface protein 1 (PfMSP1) than the controls who developed parasitemia, suggesting naturally acquired immunity against Pf limited infections in controls. This study identified a safe, protective, 4-week, multi-dose prime vaccination regimen for assessment in future trials of PfSPZ Vaccine.</description><identifier>ISSN: 0002-9637</identifier><identifier>EISSN: 1476-1645</identifier><identifier>DOI: 10.4269/ajtmh.21-0942</identifier><identifier>PMID: 35130487</identifier><language>eng</language><publisher>United States: Institute of Tropical Medicine</publisher><subject>Malaria ; Proteins ; Vaccines</subject><ispartof>The American journal of tropical medicine and hygiene, 2022-04, Vol.106 (4), p.1215-1226</ispartof><rights>Copyright Institute of Tropical Medicine Apr 2022</rights><rights>2022 by The American Society of Tropical Medicine and Hygiene 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3302-78ecca2cdd44ed9866ca85a3cb358b1d7838b77f5272cb3e6e695d51a6fe719a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8991366/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8991366/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35130487$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jongo, Said Abdallah</creatorcontrib><creatorcontrib>Church, L W Preston</creatorcontrib><creatorcontrib>Nchama, Vicente Urbano Nsue Ndong</creatorcontrib><creatorcontrib>Hamad, Ali</creatorcontrib><creatorcontrib>Chuquiyauri, Raul</creatorcontrib><creatorcontrib>Kassim, Kamaka Ramadhani</creatorcontrib><creatorcontrib>Athuman, Thabit</creatorcontrib><creatorcontrib>Deal, Anna</creatorcontrib><creatorcontrib>Natasha, K C</creatorcontrib><creatorcontrib>Mtoro, Ali</creatorcontrib><creatorcontrib>Mpina, Maxmillian</creatorcontrib><creatorcontrib>Nyakarungu, Elizabeth</creatorcontrib><creatorcontrib>Bidjimi, Gertrudis Owono</creatorcontrib><creatorcontrib>Owono, Marta Alene</creatorcontrib><creatorcontrib>Mayé, Escolástica Raquel Mansogo</creatorcontrib><creatorcontrib>Mangue, Martín Eká Ondó</creatorcontrib><creatorcontrib>Okomo, Genaro Nsué Nguema</creatorcontrib><creatorcontrib>Pasialo, Beltrán Ekuá Ntutumu</creatorcontrib><creatorcontrib>Mandumbi, Dolores Mbang Ondó</creatorcontrib><creatorcontrib>Mikue, María-Silvia A López</creatorcontrib><creatorcontrib>Mochomuemue, Fortunata Lobede</creatorcontrib><creatorcontrib>Obono, Mariano Obiang</creatorcontrib><creatorcontrib>Besahá, Juan Carlos Momo</creatorcontrib><creatorcontrib>Bijeri, José Raso</creatorcontrib><creatorcontrib>Abegue, Gabriel Mbá</creatorcontrib><creatorcontrib>Veri, Yolanda Rimoy</creatorcontrib><creatorcontrib>Bela, Ines Toichoa</creatorcontrib><creatorcontrib>Chochi, Federico Comsil</creatorcontrib><creatorcontrib>Lima Sánchez, José Enrique</creatorcontrib><creatorcontrib>Pencelli, Vanessa</creatorcontrib><creatorcontrib>Gayozo, Griselda</creatorcontrib><creatorcontrib>Nlang, José Antonio Esono Mbá</creatorcontrib><creatorcontrib>Schindler, Tobias</creatorcontrib><creatorcontrib>James, Eric R</creatorcontrib><creatorcontrib>Abebe, Yonas</creatorcontrib><creatorcontrib>Lemiale, Laurence</creatorcontrib><creatorcontrib>Stabler, Thomas C</creatorcontrib><creatorcontrib>Murshedkar, Tooba</creatorcontrib><creatorcontrib>Chen, Mei-Chun</creatorcontrib><creatorcontrib>Schwabe, Christopher</creatorcontrib><creatorcontrib>Ratsirarson, Josea</creatorcontrib><creatorcontrib>Rivas, Matilde Riloha</creatorcontrib><creatorcontrib>Ayekaba, Mitoha Ondo'o</creatorcontrib><creatorcontrib>Milang, Diosdado Vicente Nsué</creatorcontrib><creatorcontrib>Falla, Carlos Cortés</creatorcontrib><creatorcontrib>Phiri, Wonder P</creatorcontrib><creatorcontrib>García, Guillermo A</creatorcontrib><creatorcontrib>Maas, Carl D</creatorcontrib><creatorcontrib>Nlavo, Bonifacio Manguire</creatorcontrib><creatorcontrib>Tanner, Marcel</creatorcontrib><creatorcontrib>Billingsley, Peter F</creatorcontrib><creatorcontrib>Kim Lee Sim, B</creatorcontrib><creatorcontrib>Daubenberger, Claudia</creatorcontrib><creatorcontrib>Hoffman, Stephen L</creatorcontrib><creatorcontrib>Abdulla, Salim</creatorcontrib><creatorcontrib>Richie, Thomas L</creatorcontrib><title>Multi-Dose Priming Regimens of PfSPZ Vaccine: Safety and Efficacy against Controlled Human Malaria Infection in Equatoguinean Adults</title><title>The American journal of tropical medicine and hygiene</title><addtitle>Am J Trop Med Hyg</addtitle><description>Plasmodium falciparum sporozoite (PfSPZ) Vaccine is composed of radiation-attenuated, aseptic, purified cryopreserved PfSPZ. Multiple clinical trials empirically assessing two to six doses have shown multi-dose priming (two to four doses the first week) to be optimal for protection in both 4- and 16-week regimens. In this randomized, double-blind, normal saline (NS) placebo-controlled trial, four groups (G) of 18- to 32-year-old Equatoguineans received multi-dose priming regimens with or without a delayed final dose at 4 or 16 weeks. The regimens were G1: days 1, 3, 5, 7, and 113; G2: days 1, 3, 5, and 7; G3: days 1, 3, 5, 7, and 29; and G4: days 1, 8, and 29. All doses were 9 × 105 PfSPZ. Tolerability, safety, immunogenicity, and vaccine efficacy (VE) against homologous controlled human malaria infection (CHMI) 6-7 weeks after vaccination were assessed to down-select the best regimen. All four regimens were safe and well tolerated, with no significant differences in adverse events (AEs) between vaccinees (N = 84) and NS controls (N = 20) or between regimens. Out of 19 controls, 13 developed Pf parasitemia by quantitative polymerase chain reaction (qPCR) after CHMI. Only the vaccine regimen administered on study days 1, 8, and 29 gave significant protection (7/21 vaccinees versus 13/19 controls infected, VE 51.3%, P = 0.03, Barnard's test, two-tailed). There were no significant differences in antibodies against Pf circumsporozoite protein (PfCSP), a major SPZ antigen, between protected and nonprotected vaccinees or controls pre-CHMI. The six controls not developing Pf parasitemia had significantly higher antibodies to blood stage antigens Pf exported protein 1 (PfEXP1) and Pf merozoite surface protein 1 (PfMSP1) than the controls who developed parasitemia, suggesting naturally acquired immunity against Pf limited infections in controls. This study identified a safe, protective, 4-week, multi-dose prime vaccination regimen for assessment in future trials of PfSPZ 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L</creator><creator>Abdulla, Salim</creator><creator>Richie, Thomas L</creator><general>Institute of Tropical Medicine</general><general>The American Society of Tropical Medicine and Hygiene</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20220406</creationdate><title>Multi-Dose Priming Regimens of PfSPZ Vaccine: Safety and Efficacy against Controlled Human Malaria Infection in Equatoguinean Adults</title><author>Jongo, Said Abdallah ; Church, L W Preston ; Nchama, Vicente Urbano Nsue Ndong ; Hamad, Ali ; Chuquiyauri, Raul ; Kassim, Kamaka Ramadhani ; Athuman, Thabit ; Deal, Anna ; Natasha, K C ; Mtoro, Ali ; Mpina, Maxmillian ; Nyakarungu, Elizabeth ; Bidjimi, Gertrudis Owono ; Owono, Marta Alene ; Mayé, Escolástica Raquel Mansogo ; Mangue, Martín Eká Ondó ; Okomo, Genaro Nsué Nguema ; Pasialo, Beltrán Ekuá Ntutumu ; Mandumbi, Dolores Mbang Ondó ; Mikue, María-Silvia A López ; Mochomuemue, Fortunata Lobede ; Obono, Mariano Obiang ; Besahá, Juan Carlos Momo ; Bijeri, José Raso ; Abegue, Gabriel Mbá ; Veri, Yolanda Rimoy ; Bela, Ines Toichoa ; Chochi, Federico Comsil ; Lima Sánchez, José Enrique ; Pencelli, Vanessa ; Gayozo, Griselda ; Nlang, José Antonio Esono Mbá ; Schindler, Tobias ; James, Eric R ; Abebe, Yonas ; Lemiale, Laurence ; Stabler, Thomas C ; Murshedkar, Tooba ; Chen, Mei-Chun ; Schwabe, Christopher ; Ratsirarson, Josea ; Rivas, Matilde Riloha ; Ayekaba, Mitoha Ondo'o ; Milang, Diosdado Vicente Nsué ; Falla, Carlos Cortés ; Phiri, Wonder P ; García, Guillermo A ; Maas, Carl D ; Nlavo, Bonifacio Manguire ; Tanner, Marcel ; Billingsley, Peter F ; Kim Lee Sim, B ; Daubenberger, Claudia ; Hoffman, Stephen L ; Abdulla, Salim ; Richie, Thomas L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3302-78ecca2cdd44ed9866ca85a3cb358b1d7838b77f5272cb3e6e695d51a6fe719a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Malaria</topic><topic>Proteins</topic><topic>Vaccines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jongo, Said Abdallah</creatorcontrib><creatorcontrib>Church, L W Preston</creatorcontrib><creatorcontrib>Nchama, Vicente Urbano Nsue Ndong</creatorcontrib><creatorcontrib>Hamad, Ali</creatorcontrib><creatorcontrib>Chuquiyauri, Raul</creatorcontrib><creatorcontrib>Kassim, Kamaka Ramadhani</creatorcontrib><creatorcontrib>Athuman, Thabit</creatorcontrib><creatorcontrib>Deal, Anna</creatorcontrib><creatorcontrib>Natasha, K C</creatorcontrib><creatorcontrib>Mtoro, Ali</creatorcontrib><creatorcontrib>Mpina, Maxmillian</creatorcontrib><creatorcontrib>Nyakarungu, Elizabeth</creatorcontrib><creatorcontrib>Bidjimi, Gertrudis Owono</creatorcontrib><creatorcontrib>Owono, Marta Alene</creatorcontrib><creatorcontrib>Mayé, Escolástica Raquel Mansogo</creatorcontrib><creatorcontrib>Mangue, Martín Eká Ondó</creatorcontrib><creatorcontrib>Okomo, Genaro Nsué Nguema</creatorcontrib><creatorcontrib>Pasialo, Beltrán Ekuá Ntutumu</creatorcontrib><creatorcontrib>Mandumbi, Dolores Mbang Ondó</creatorcontrib><creatorcontrib>Mikue, María-Silvia A López</creatorcontrib><creatorcontrib>Mochomuemue, Fortunata Lobede</creatorcontrib><creatorcontrib>Obono, Mariano Obiang</creatorcontrib><creatorcontrib>Besahá, Juan Carlos Momo</creatorcontrib><creatorcontrib>Bijeri, José Raso</creatorcontrib><creatorcontrib>Abegue, Gabriel Mbá</creatorcontrib><creatorcontrib>Veri, Yolanda Rimoy</creatorcontrib><creatorcontrib>Bela, Ines Toichoa</creatorcontrib><creatorcontrib>Chochi, Federico Comsil</creatorcontrib><creatorcontrib>Lima Sánchez, José Enrique</creatorcontrib><creatorcontrib>Pencelli, Vanessa</creatorcontrib><creatorcontrib>Gayozo, Griselda</creatorcontrib><creatorcontrib>Nlang, José Antonio Esono Mbá</creatorcontrib><creatorcontrib>Schindler, Tobias</creatorcontrib><creatorcontrib>James, Eric R</creatorcontrib><creatorcontrib>Abebe, Yonas</creatorcontrib><creatorcontrib>Lemiale, Laurence</creatorcontrib><creatorcontrib>Stabler, Thomas C</creatorcontrib><creatorcontrib>Murshedkar, Tooba</creatorcontrib><creatorcontrib>Chen, Mei-Chun</creatorcontrib><creatorcontrib>Schwabe, Christopher</creatorcontrib><creatorcontrib>Ratsirarson, Josea</creatorcontrib><creatorcontrib>Rivas, Matilde Riloha</creatorcontrib><creatorcontrib>Ayekaba, Mitoha Ondo'o</creatorcontrib><creatorcontrib>Milang, Diosdado Vicente Nsué</creatorcontrib><creatorcontrib>Falla, Carlos Cortés</creatorcontrib><creatorcontrib>Phiri, Wonder P</creatorcontrib><creatorcontrib>García, Guillermo A</creatorcontrib><creatorcontrib>Maas, Carl D</creatorcontrib><creatorcontrib>Nlavo, Bonifacio Manguire</creatorcontrib><creatorcontrib>Tanner, Marcel</creatorcontrib><creatorcontrib>Billingsley, Peter F</creatorcontrib><creatorcontrib>Kim Lee Sim, B</creatorcontrib><creatorcontrib>Daubenberger, Claudia</creatorcontrib><creatorcontrib>Hoffman, Stephen L</creatorcontrib><creatorcontrib>Abdulla, Salim</creatorcontrib><creatorcontrib>Richie, Thomas L</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of tropical medicine and hygiene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jongo, Said Abdallah</au><au>Church, L W Preston</au><au>Nchama, Vicente Urbano Nsue Ndong</au><au>Hamad, Ali</au><au>Chuquiyauri, Raul</au><au>Kassim, Kamaka Ramadhani</au><au>Athuman, Thabit</au><au>Deal, Anna</au><au>Natasha, K C</au><au>Mtoro, Ali</au><au>Mpina, Maxmillian</au><au>Nyakarungu, Elizabeth</au><au>Bidjimi, Gertrudis Owono</au><au>Owono, Marta Alene</au><au>Mayé, Escolástica Raquel Mansogo</au><au>Mangue, Martín Eká Ondó</au><au>Okomo, Genaro Nsué Nguema</au><au>Pasialo, Beltrán Ekuá Ntutumu</au><au>Mandumbi, Dolores Mbang Ondó</au><au>Mikue, María-Silvia A López</au><au>Mochomuemue, Fortunata Lobede</au><au>Obono, Mariano Obiang</au><au>Besahá, Juan Carlos Momo</au><au>Bijeri, José Raso</au><au>Abegue, Gabriel Mbá</au><au>Veri, Yolanda Rimoy</au><au>Bela, Ines Toichoa</au><au>Chochi, Federico Comsil</au><au>Lima Sánchez, José Enrique</au><au>Pencelli, Vanessa</au><au>Gayozo, Griselda</au><au>Nlang, José Antonio Esono Mbá</au><au>Schindler, Tobias</au><au>James, Eric R</au><au>Abebe, Yonas</au><au>Lemiale, Laurence</au><au>Stabler, Thomas C</au><au>Murshedkar, Tooba</au><au>Chen, Mei-Chun</au><au>Schwabe, Christopher</au><au>Ratsirarson, Josea</au><au>Rivas, Matilde Riloha</au><au>Ayekaba, Mitoha Ondo'o</au><au>Milang, Diosdado Vicente Nsué</au><au>Falla, Carlos Cortés</au><au>Phiri, Wonder P</au><au>García, Guillermo A</au><au>Maas, Carl D</au><au>Nlavo, Bonifacio Manguire</au><au>Tanner, Marcel</au><au>Billingsley, Peter F</au><au>Kim Lee Sim, B</au><au>Daubenberger, Claudia</au><au>Hoffman, Stephen L</au><au>Abdulla, Salim</au><au>Richie, Thomas L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multi-Dose Priming Regimens of PfSPZ Vaccine: Safety and Efficacy against Controlled Human Malaria Infection in Equatoguinean Adults</atitle><jtitle>The American journal of tropical medicine and hygiene</jtitle><addtitle>Am J Trop Med Hyg</addtitle><date>2022-04-06</date><risdate>2022</risdate><volume>106</volume><issue>4</issue><spage>1215</spage><epage>1226</epage><pages>1215-1226</pages><issn>0002-9637</issn><eissn>1476-1645</eissn><abstract>Plasmodium falciparum sporozoite (PfSPZ) Vaccine is composed of radiation-attenuated, aseptic, purified cryopreserved PfSPZ. Multiple clinical trials empirically assessing two to six doses have shown multi-dose priming (two to four doses the first week) to be optimal for protection in both 4- and 16-week regimens. In this randomized, double-blind, normal saline (NS) placebo-controlled trial, four groups (G) of 18- to 32-year-old Equatoguineans received multi-dose priming regimens with or without a delayed final dose at 4 or 16 weeks. The regimens were G1: days 1, 3, 5, 7, and 113; G2: days 1, 3, 5, and 7; G3: days 1, 3, 5, 7, and 29; and G4: days 1, 8, and 29. All doses were 9 × 105 PfSPZ. Tolerability, safety, immunogenicity, and vaccine efficacy (VE) against homologous controlled human malaria infection (CHMI) 6-7 weeks after vaccination were assessed to down-select the best regimen. All four regimens were safe and well tolerated, with no significant differences in adverse events (AEs) between vaccinees (N = 84) and NS controls (N = 20) or between regimens. Out of 19 controls, 13 developed Pf parasitemia by quantitative polymerase chain reaction (qPCR) after CHMI. Only the vaccine regimen administered on study days 1, 8, and 29 gave significant protection (7/21 vaccinees versus 13/19 controls infected, VE 51.3%, P = 0.03, Barnard's test, two-tailed). There were no significant differences in antibodies against Pf circumsporozoite protein (PfCSP), a major SPZ antigen, between protected and nonprotected vaccinees or controls pre-CHMI. The six controls not developing Pf parasitemia had significantly higher antibodies to blood stage antigens Pf exported protein 1 (PfEXP1) and Pf merozoite surface protein 1 (PfMSP1) than the controls who developed parasitemia, suggesting naturally acquired immunity against Pf limited infections in controls. This study identified a safe, protective, 4-week, multi-dose prime vaccination regimen for assessment in future trials of PfSPZ Vaccine.</abstract><cop>United States</cop><pub>Institute of Tropical Medicine</pub><pmid>35130487</pmid><doi>10.4269/ajtmh.21-0942</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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subjects Malaria
Proteins
Vaccines
title Multi-Dose Priming Regimens of PfSPZ Vaccine: Safety and Efficacy against Controlled Human Malaria Infection in Equatoguinean Adults
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