Novel Surrogate Neutralizing Assay Supports Parvovirus B19 Vaccine Development for Children with Sickle Cell Disease.

VP1u aplastic crisis enzyme-linked immunosorbent assay neutralization assay parvovirus B19 sickle cell disease vaccine

Journal

Vaccines
ISSN: 2076-393X
Titre abrégé: Vaccines (Basel)
Pays: Switzerland
ID NLM: 101629355

Informations de publication

Date de publication:
04 Aug 2021
Historique:
received: 13 06 2021
revised: 27 07 2021
accepted: 27 07 2021
entrez: 28 8 2021
pubmed: 29 8 2021
medline: 29 8 2021
Statut: epublish

Résumé

Children with sickle cell disease (SCD) suffer life-threatening transient aplastic crisis (TAC) when infected with parvovirus B19. In utero, infection of healthy fetuses may result in anemia, hydrops, and death. Unfortunately, although promising vaccine candidates exist, no product has yet been licensed. One barrier to vaccine development has been the lack of a cost-effective, standardized parvovirus B19 neutralization assay. To fill this void, we evaluated the unique region of VP1 (VP1u), which contains prominent targets of neutralizing antibodies. We discovered an antigenic cross-reactivity between VP1 and VP2 that, at first, thwarted the development of a surrogate neutralization assay. We overcame the cross-reactivity by designing a mutated VP1u (VP1uAT) fragment. A new VP1uAT ELISA yielded results well correlated with neutralization (Spearman's correlation coefficient = 0.581;

Identifiants

pubmed: 34451986
pii: vaccines9080860
doi: 10.3390/vaccines9080860
pmc: PMC8402426
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NCI NIH HHS
ID : P30 CA21765
Pays : United States
Organisme : American Lebanese Syrian Associated Charities
ID : ALSAC
Organisme : Children's Infection Defense Center at St. Jude Children's Research Hospital
ID : CIDC
Organisme : Intramural Research Program of NHLBI, NIH
ID : NHLBI
Organisme : Novartis Vaccines and Diagnostics
ID : Novartis

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Auteurs

Rhiannon R Penkert (RR)

Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

Sumana Chandramouli (S)

Novartis Vaccines and Diagnostics, Cambridge, MA 02139, USA.

Philip R Dormitzer (PR)

Novartis Vaccines and Diagnostics, Cambridge, MA 02139, USA.

Ethan C Settembre (EC)

Novartis Vaccines and Diagnostics, Cambridge, MA 02139, USA.

Robert E Sealy (RE)

Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

Susan Wong (S)

Hematology Branch, National Heart, Lung and Blood Institute, Bethesda, MD 20892, USA.

Neal S Young (NS)

Hematology Branch, National Heart, Lung and Blood Institute, Bethesda, MD 20892, USA.

Yilun Sun (Y)

Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

Li Tang (L)

Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

Alyssa Cotton (A)

Department of Hematology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

Jola Dowdy (J)

Department of Hematology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

Randall T Hayden (RT)

Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

Jane S Hankins (JS)

Department of Hematology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

Julia L Hurwitz (JL)

Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Department of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, TN 38163, USA.

Classifications MeSH