The Humoral Immune Response Against the gB Vaccine: Lessons Learnt from Protection in Solid Organ Transplantation

Human cytomegalovirus (hCMV) is considered to be the highest priority for vaccine development. This view is underscored by the significant morbidity associated with congenital hCMV infection and viraemia in transplant patients. Although a number of vaccines have been trialed, none have been licensed...

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Main Authors: Ariane C. Gomes, Paul D. Griffiths, Matthew B. Reeves
Format: Article
Language:English
Published: MDPI AG 2019-07-01
Series:Vaccines
Subjects:
gB
Online Access:https://www.mdpi.com/2076-393X/7/3/67
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spelling doaj-b02a675f791346578f2a5cd8e42f98be2020-11-24T20:53:44ZengMDPI AGVaccines2076-393X2019-07-01736710.3390/vaccines7030067vaccines7030067The Humoral Immune Response Against the gB Vaccine: Lessons Learnt from Protection in Solid Organ TransplantationAriane C. Gomes0Paul D. Griffiths1Matthew B. Reeves2Institute for Immunity and Transplantation, University College London, London NW3 2PF, UKInstitute for Immunity and Transplantation, University College London, London NW3 2PF, UKInstitute for Immunity and Transplantation, University College London, London NW3 2PF, UKHuman cytomegalovirus (hCMV) is considered to be the highest priority for vaccine development. This view is underscored by the significant morbidity associated with congenital hCMV infection and viraemia in transplant patients. Although a number of vaccines have been trialed, none have been licensed. The hCMV vaccine candidate that has performed best in clinical trials to date is the recombinant glycoprotein B (gB) vaccine that has demonstrated protection, ranging from a 43% to 50% efficacy in three independent phase II trials. In this review, we focus on data from the phase II trial performed in solid organ transplant patients and the outcomes of follow-up studies attempting to identify immunological and mechanistic correlates of protection associated with this vaccine strategy. We relate this to other vaccine studies of gB as well as other vaccine strategies to determine areas of commonality and divergence. Finally, through the review, we discuss the unique challenges and opportunities presented with vaccine studies in transplant populations with recommendations that could empower subsequent trials.https://www.mdpi.com/2076-393X/7/3/67cytomegalovirusvaccineantibodiesgB
collection DOAJ
language English
format Article
sources DOAJ
author Ariane C. Gomes
Paul D. Griffiths
Matthew B. Reeves
spellingShingle Ariane C. Gomes
Paul D. Griffiths
Matthew B. Reeves
The Humoral Immune Response Against the gB Vaccine: Lessons Learnt from Protection in Solid Organ Transplantation
Vaccines
cytomegalovirus
vaccine
antibodies
gB
author_facet Ariane C. Gomes
Paul D. Griffiths
Matthew B. Reeves
author_sort Ariane C. Gomes
title The Humoral Immune Response Against the gB Vaccine: Lessons Learnt from Protection in Solid Organ Transplantation
title_short The Humoral Immune Response Against the gB Vaccine: Lessons Learnt from Protection in Solid Organ Transplantation
title_full The Humoral Immune Response Against the gB Vaccine: Lessons Learnt from Protection in Solid Organ Transplantation
title_fullStr The Humoral Immune Response Against the gB Vaccine: Lessons Learnt from Protection in Solid Organ Transplantation
title_full_unstemmed The Humoral Immune Response Against the gB Vaccine: Lessons Learnt from Protection in Solid Organ Transplantation
title_sort humoral immune response against the gb vaccine: lessons learnt from protection in solid organ transplantation
publisher MDPI AG
series Vaccines
issn 2076-393X
publishDate 2019-07-01
description Human cytomegalovirus (hCMV) is considered to be the highest priority for vaccine development. This view is underscored by the significant morbidity associated with congenital hCMV infection and viraemia in transplant patients. Although a number of vaccines have been trialed, none have been licensed. The hCMV vaccine candidate that has performed best in clinical trials to date is the recombinant glycoprotein B (gB) vaccine that has demonstrated protection, ranging from a 43% to 50% efficacy in three independent phase II trials. In this review, we focus on data from the phase II trial performed in solid organ transplant patients and the outcomes of follow-up studies attempting to identify immunological and mechanistic correlates of protection associated with this vaccine strategy. We relate this to other vaccine studies of gB as well as other vaccine strategies to determine areas of commonality and divergence. Finally, through the review, we discuss the unique challenges and opportunities presented with vaccine studies in transplant populations with recommendations that could empower subsequent trials.
topic cytomegalovirus
vaccine
antibodies
gB
url https://www.mdpi.com/2076-393X/7/3/67
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