Safety and Immunogenicity of Radiation-Attenuated PfSPZ Vaccine in Equatoguinean Infants, Children, and Adults
The radiation-attenuated Plasmodium falciparum sporozoites (PfSPZ) Vaccine has demonstrated safety and immunogenicity in 5-month-old to 50-year-old Africans in multiple trials. Except for one, each trial has restricted enrollment to either infants and children or adults < 50 years old. This trial...
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creator | Jongo, Said A Urbano Nsue Ndong Nchama, Vicente Church, L W Preston Olotu, Ally Manock, Stephen R Schindler, Tobias Mtoro, Ali Kc, Natasha Devinsky, Orrin Zan, Elcin Hamad, Ali Nyakarungu, Elizabeth Mpina, Maxmillian Deal, Anna Bijeri, José Raso Ondo Mangue, Martin Eka Ntutumu Pasialo, Beltrán Ekua Nguema, Genaro Nsue Rivas, Matilde Riloha Chemba, Mwajuma Ramadhani, Kamaka K James, Eric R Stabler, Thomas C Abebe, Yonas Riyahi, Pouria Saverino, Elizabeth S Sax, Julian Hosch, Salome Tumbo, Anneth Gondwe, Linda Segura, J Luis Falla, Carlos Cortes Phiri, Wonder Philip Hergott, Dianna E B García, Guillermo A Maas, Carl Murshedkar, Tooba Billingsley, Peter F Tanner, Marcel Ayekaba, Mitoha Ondo'o Sim, B Kim Lee Daubenberger, Claudia Richie, Thomas L Abdulla, Salim Hoffman, Stephen L |
description | The radiation-attenuated Plasmodium falciparum sporozoites (PfSPZ) Vaccine has demonstrated safety and immunogenicity in 5-month-old to 50-year-old Africans in multiple trials. Except for one, each trial has restricted enrollment to either infants and children or adults < 50 years old. This trial was conducted in Equatorial Guinea and assessed the safety, tolerability, and immunogenicity of three direct venous inoculations of 1.8 × 106 or 2.7 × 106 PfSPZ, of PfSPZ Vaccine, or normal saline administered at 8-week intervals in a randomized, double-blind, placebo-controlled trial stratified by age (6-11 months and 1-5, 6-10, 11-17, 18-35, and 36-61 years). All doses were successfully administered. In all, 192/207 injections (93%) in those aged 6-61 years were rated as causing no or mild pain. There were no significant differences in solicited adverse events (AEs) between vaccinees and controls in any age group (P ≥ 0.17). There were no significant differences between vaccinees and controls with respect to the rates or severity of unsolicited AEs or laboratory abnormalities. Development of antibodies to P. falciparum circumsporozoite protein occurred in 67/69 vaccinees (97%) and 0/15 controls. Median antibody levels were highest in infants and 1-5-year-olds and declined progressively with age. Antibody responses in children were greater than in adults protected against controlled human malaria infection. Robust immunogenicity, combined with a benign AE profile, indicates children are an ideal target for immunization with PfSPZ Vaccine. |
doi_str_mv | 10.4269/ajtmh.22-0773 |
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Except for one, each trial has restricted enrollment to either infants and children or adults < 50 years old. This trial was conducted in Equatorial Guinea and assessed the safety, tolerability, and immunogenicity of three direct venous inoculations of 1.8 × 106 or 2.7 × 106 PfSPZ, of PfSPZ Vaccine, or normal saline administered at 8-week intervals in a randomized, double-blind, placebo-controlled trial stratified by age (6-11 months and 1-5, 6-10, 11-17, 18-35, and 36-61 years). All doses were successfully administered. In all, 192/207 injections (93%) in those aged 6-61 years were rated as causing no or mild pain. There were no significant differences in solicited adverse events (AEs) between vaccinees and controls in any age group (P ≥ 0.17). There were no significant differences between vaccinees and controls with respect to the rates or severity of unsolicited AEs or laboratory abnormalities. Development of antibodies to P. falciparum circumsporozoite protein occurred in 67/69 vaccinees (97%) and 0/15 controls. Median antibody levels were highest in infants and 1-5-year-olds and declined progressively with age. Antibody responses in children were greater than in adults protected against controlled human malaria infection. Robust immunogenicity, combined with a benign AE profile, indicates children are an ideal target for immunization with PfSPZ Vaccine.</description><identifier>ISSN: 0002-9637</identifier><identifier>EISSN: 1476-1645</identifier><identifier>DOI: 10.4269/ajtmh.22-0773</identifier><identifier>PMID: 37160281</identifier><language>eng</language><publisher>United States: Institute of Tropical Medicine</publisher><subject>Age groups ; Antibodies ; Clinical trials ; Disease transmission ; Immunity (Disease) ; Malaria ; Parasites ; Radiation ; Side effects ; Vaccines</subject><ispartof>The American journal of tropical medicine and hygiene, 2023-07, Vol.109 (1), p.138-146</ispartof><rights>Copyright Institute of Tropical Medicine Jul 2023</rights><rights>The author(s) 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-d78c70c3b0bff4b6c06aed76a1b4a028179d83f336728f89cfcd5ec23fd2a0983</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/PMC10324022/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324022/$$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/37160281$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jongo, Said A</creatorcontrib><creatorcontrib>Urbano Nsue Ndong Nchama, Vicente</creatorcontrib><creatorcontrib>Church, L W Preston</creatorcontrib><creatorcontrib>Olotu, Ally</creatorcontrib><creatorcontrib>Manock, Stephen R</creatorcontrib><creatorcontrib>Schindler, Tobias</creatorcontrib><creatorcontrib>Mtoro, Ali</creatorcontrib><creatorcontrib>Kc, Natasha</creatorcontrib><creatorcontrib>Devinsky, Orrin</creatorcontrib><creatorcontrib>Zan, Elcin</creatorcontrib><creatorcontrib>Hamad, Ali</creatorcontrib><creatorcontrib>Nyakarungu, Elizabeth</creatorcontrib><creatorcontrib>Mpina, Maxmillian</creatorcontrib><creatorcontrib>Deal, Anna</creatorcontrib><creatorcontrib>Bijeri, José Raso</creatorcontrib><creatorcontrib>Ondo Mangue, Martin Eka</creatorcontrib><creatorcontrib>Ntutumu Pasialo, Beltrán Ekua</creatorcontrib><creatorcontrib>Nguema, Genaro Nsue</creatorcontrib><creatorcontrib>Rivas, Matilde Riloha</creatorcontrib><creatorcontrib>Chemba, Mwajuma</creatorcontrib><creatorcontrib>Ramadhani, Kamaka K</creatorcontrib><creatorcontrib>James, Eric R</creatorcontrib><creatorcontrib>Stabler, Thomas C</creatorcontrib><creatorcontrib>Abebe, Yonas</creatorcontrib><creatorcontrib>Riyahi, Pouria</creatorcontrib><creatorcontrib>Saverino, Elizabeth S</creatorcontrib><creatorcontrib>Sax, Julian</creatorcontrib><creatorcontrib>Hosch, Salome</creatorcontrib><creatorcontrib>Tumbo, Anneth</creatorcontrib><creatorcontrib>Gondwe, Linda</creatorcontrib><creatorcontrib>Segura, J Luis</creatorcontrib><creatorcontrib>Falla, Carlos Cortes</creatorcontrib><creatorcontrib>Phiri, Wonder Philip</creatorcontrib><creatorcontrib>Hergott, Dianna E B</creatorcontrib><creatorcontrib>García, Guillermo A</creatorcontrib><creatorcontrib>Maas, Carl</creatorcontrib><creatorcontrib>Murshedkar, Tooba</creatorcontrib><creatorcontrib>Billingsley, Peter F</creatorcontrib><creatorcontrib>Tanner, Marcel</creatorcontrib><creatorcontrib>Ayekaba, Mitoha Ondo'o</creatorcontrib><creatorcontrib>Sim, B Kim Lee</creatorcontrib><creatorcontrib>Daubenberger, Claudia</creatorcontrib><creatorcontrib>Richie, Thomas L</creatorcontrib><creatorcontrib>Abdulla, Salim</creatorcontrib><creatorcontrib>Hoffman, Stephen L</creatorcontrib><title>Safety and Immunogenicity of Radiation-Attenuated PfSPZ Vaccine in Equatoguinean Infants, Children, and Adults</title><title>The American journal of tropical medicine and hygiene</title><addtitle>Am J Trop Med Hyg</addtitle><description>The radiation-attenuated Plasmodium falciparum sporozoites (PfSPZ) Vaccine has demonstrated safety and immunogenicity in 5-month-old to 50-year-old Africans in multiple trials. Except for one, each trial has restricted enrollment to either infants and children or adults < 50 years old. This trial was conducted in Equatorial Guinea and assessed the safety, tolerability, and immunogenicity of three direct venous inoculations of 1.8 × 106 or 2.7 × 106 PfSPZ, of PfSPZ Vaccine, or normal saline administered at 8-week intervals in a randomized, double-blind, placebo-controlled trial stratified by age (6-11 months and 1-5, 6-10, 11-17, 18-35, and 36-61 years). All doses were successfully administered. In all, 192/207 injections (93%) in those aged 6-61 years were rated as causing no or mild pain. There were no significant differences in solicited adverse events (AEs) between vaccinees and controls in any age group (P ≥ 0.17). There were no significant differences between vaccinees and controls with respect to the rates or severity of unsolicited AEs or laboratory abnormalities. Development of antibodies to P. falciparum circumsporozoite protein occurred in 67/69 vaccinees (97%) and 0/15 controls. Median antibody levels were highest in infants and 1-5-year-olds and declined progressively with age. Antibody responses in children were greater than in adults protected against controlled human malaria infection. Robust immunogenicity, combined with a benign AE profile, indicates children are an ideal target for immunization with PfSPZ Vaccine.</description><subject>Age groups</subject><subject>Antibodies</subject><subject>Clinical trials</subject><subject>Disease transmission</subject><subject>Immunity (Disease)</subject><subject>Malaria</subject><subject>Parasites</subject><subject>Radiation</subject><subject>Side 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Except for one, each trial has restricted enrollment to either infants and children or adults < 50 years old. This trial was conducted in Equatorial Guinea and assessed the safety, tolerability, and immunogenicity of three direct venous inoculations of 1.8 × 106 or 2.7 × 106 PfSPZ, of PfSPZ Vaccine, or normal saline administered at 8-week intervals in a randomized, double-blind, placebo-controlled trial stratified by age (6-11 months and 1-5, 6-10, 11-17, 18-35, and 36-61 years). All doses were successfully administered. In all, 192/207 injections (93%) in those aged 6-61 years were rated as causing no or mild pain. There were no significant differences in solicited adverse events (AEs) between vaccinees and controls in any age group (P ≥ 0.17). There were no significant differences between vaccinees and controls with respect to the rates or severity of unsolicited AEs or laboratory abnormalities. Development of antibodies to P. falciparum circumsporozoite protein occurred in 67/69 vaccinees (97%) and 0/15 controls. Median antibody levels were highest in infants and 1-5-year-olds and declined progressively with age. Antibody responses in children were greater than in adults protected against controlled human malaria infection. Robust immunogenicity, combined with a benign AE profile, indicates children are an ideal target for immunization with PfSPZ Vaccine.</abstract><cop>United States</cop><pub>Institute of Tropical Medicine</pub><pmid>37160281</pmid><doi>10.4269/ajtmh.22-0773</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection |
subjects | Age groups Antibodies Clinical trials Disease transmission Immunity (Disease) Malaria Parasites Radiation Side effects Vaccines |
title | Safety and Immunogenicity of Radiation-Attenuated PfSPZ Vaccine in Equatoguinean Infants, Children, and Adults |
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