Publication:
Immunogenicity of the Conjugate Meningococcal ACWY-TT Vaccine in Children and Adolescents Living with HIV

dc.contributor.authorBerzosa, Arantxa
dc.contributor.authorGuillen, Sara
dc.contributor.authorEpalza, Cristina
dc.contributor.authorEscosa, Luis
dc.contributor.authorNavarro, Maria Luisa
dc.contributor.authorPrieto, Luis M
dc.contributor.authorSainz, Talia
dc.contributor.authorJimenez de Ory, Santiago
dc.contributor.authorMontes Mota, Marina
dc.contributor.authorAbad, Raquel
dc.contributor.authorVazquez-Moreno, Julio Alberto
dc.contributor.authorSerrano García, Irene
dc.contributor.authorRamos-Amador, José Tomás
dc.contributor.funderFundación Familia Alonso
dc.contributor.funderRETICS-Sida (RIS-ISCIII) (España)
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderCentro de Investigación Biomédica en Red - CIBERINFEC (Enfermedades Infecciosas)
dc.contributor.funderEuropean Society for Paediatric Infectious Diseases
dc.date.accessioned2025-03-26T14:19:01Z
dc.date.available2025-03-26T14:19:01Z
dc.date.issued2024
dc.description.abstractBackground: Children and adolescents living with HIV (CALHIV) are at high risk of meningococcal infections and may present lower immune responses to vaccines. The objectives of this study were to assess the immunogenicity of the quadrivalent Men ACWY-TT vaccine (Nimenrix®) in CALHIV after a two-dose schedule and to describe possible HIV-related factors that may affect the immunogenic response. Methods: A multicenter prospective study was designed, including CALHIV followed in five hospitals in Madrid, between 2019 and 2021. Two doses of the Men ACWY-TT vaccine were administered. Serum bactericidal antibody (SBA) assays using rabbit complement (rSBA) against serogroups C, W, and Y were used to determine seroprotection and vaccine response (the proportion achieving a putative protective titer of ≥eight or a ≥four-fold rise in titer from baseline). Serum was collected at baseline, and at 3 and 12 months after vaccination. Results: There were 29 CALHIV included, 76% of whom were perinatally infected. All were receiving TAR and presented a good immunovirological and clinical status overall. At baseline, 45% of CALHIV had seroprotective titers to at least one serogroup, with individual seroprotection rates of 24%, 28%, and 32% against C, W, and Y, respectively. After a two-dose schedule, vaccine response was 83% for each serogroup, eliciting a vaccine response to all serogroups in 69% of them. One year after vaccination, 75% of CALHIV maintained seroprotective titers against the C serogroup, and 96% against W and Y. None of the HIV-related characteristics analyzed could predict vaccine response or antibody duration. Conclusions: CALHIV who received effective TAR and presented a good immuno-virological situation achieved an appropriate vaccine response after two doses of the Men ACWY-TT vaccine, and antibody-mediated protection against serogroups C, W, and Y was maintained in more than 70% of the patients one year after vaccination.
dc.description.peerreviewed
dc.description.sponsorshipFamilia Alonso Foundation had funded this study (JRA.C01ALO). CoRISpe is integrated in the Spanish AIDS Research Network (RIS), supported by the Instituto de Salud Carlos III (Grant nº RD06/0006/0034 and nº RD06/0006/0035). Networking research center CIBER infectious diseases ISCIII (CB21/13/00077) collaborated founding this project. T.S. has been funded by a Springboard Award of the European Society of Pediatric Infectious Diseases (ESPID).
dc.format.number1
dc.format.page30
dc.format.volume12
dc.identifier.citationBerzosa A, Guillen S, Epalza C, Escosa L, Navarro ML, Prieto LM, Sainz T, de Ory SJ, Montes M, Abad R, Vázquez JA, García IS, Ramos-Amador JT. Immunogenicity of the Conjugate Meningococcal ACWY-TT Vaccine in Children and Adolescents Living with HIV. Microorganisms. 2024;12(1):30.
dc.identifier.doi10.3390/microorganisms12010030
dc.identifier.e-issn2076-2607
dc.identifier.journalMicroorganisms
dc.identifier.pubmedID38257857
dc.identifier.urihttps://hdl.handle.net/20.500.12105/26579
dc.language.isoeng
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD06/0006/0034
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD06/0006/0035
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/CB21/13/00077
dc.relation.publisherversionhttps://doi.org/10.3390/microorganisms12010030
dc.repisalud.centroISCIII::Centro Nacional de Microbiología (CNM)
dc.repisalud.institucionISCIII
dc.repisalud.instituteIIS::IdISSC - Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (Madrid)
dc.repisalud.instituteIIS::IdiPAZ - Instituto de Investigación Sanitaria Hospital La Paz (Madrid)
dc.repisalud.instituteIIS::IiSGM - Instituto de Investigación Sanitaria Gregorio Marañón (Madrid)
dc.rights.accessRightsopen access
dc.rights.licenseAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectHIV
dc.subjectMen ACWY-TT vaccines
dc.subjectMeningococcal infection
dc.subjectVaccine response
dc.titleImmunogenicity of the Conjugate Meningococcal ACWY-TT Vaccine in Children and Adolescents Living with HIV
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication
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