Are International Units of Anti-HBs Antibodies Always Indicative of Hepatitis B Virus Neutralizing Activity?

HBV infectivity neutralization HBV vaccine anti-HBs international units anti-HBs neutralizing activity

Journal

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

Informations de publication

Date de publication:
04 Apr 2023
Historique:
received: 06 03 2023
revised: 31 03 2023
accepted: 01 04 2023
medline: 28 4 2023
pubmed: 28 4 2023
entrez: 28 4 2023
Statut: epublish

Résumé

Anti-HBs antibodies are elicited upon hepatitis B vaccination, and concentrations above 10 mIU/mL are considered protective. Our aim was to assess the relationship between IU/mL of anti-HBs and neutralization activity. Immunoglobulins G (IgGs) were purified from individuals who received a serum-derived vaccine (Group 1), a recombinant vaccine, Genevac-B or Engerix-B (Group 2), or who recovered from acute infection (Group 3). IgGs were tested for anti-HBs, anti-preS1, and anti-preS2 antibodies and for their neutralizing activity in an in vitro infection assay. Anti-HBs IUs/mL value did not strictly correlate with neutralization activity. The Group 1 antibodies demonstrated a greater neutralizing activity than those of Group 2. Anti-preS1 antibodies were detected in Groups 1 and 3, and anti-preS2 in Group 1 and Group 2/Genhevac-B, but the contribution of anti-preS antibodies to neutralization could not be demonstrated. Virions bearing immune escape HBsAg variants were less susceptible to neutralization than wild-type virions. The level of anti-HBs antibodies in IUs is not sufficient to assess neutralizing activity. Consequently, (i) an in vitro neutralization assay should be included in the quality control procedures of antibody preparations intended for HB prophylaxis or immunotherapy, and (ii) a greater emphasis should be placed on ensuring that vaccine genotype/subtype matches with that of the circulating HBV.

Identifiants

pubmed: 37112703
pii: vaccines11040791
doi: 10.3390/vaccines11040791
pmc: PMC10147002
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Maladies infectieuses émergentes
ID : ANRS MIE ECTZ117561

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Auteurs

Yada Aronthippaitoon (Y)

Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50100, Thailand.
LUCENT International Collaboration, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50100, Thailand.

Nathan Szerman (N)

Laboratoire de Bactériologie-Virologie-Hygiène, CHRU, Université of Tours, INSERM U1259, 37044 Tours, France.

Nicole Ngo-Giang-Huong (N)

Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50100, Thailand.
LUCENT International Collaboration, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50100, Thailand.
Institut de Recherche pour le Développement (IRD), MIVEGEC, CNRS, Agropolis, University of Montpellier, 34394 Montpellier, France.

Syria Laperche (S)

Institut National de la Transfusion Sanguine, CNR Risques Infectieux Transfusionnels, 75015 Paris, France.
Etablissement Français du Sang, La Plaine, 93218 Saint-Denis, France.

Marie-Noelle Ungeheuer (MN)

Center for Translational Science, ICAReB, Institut Pasteur, 75015 Paris, France.

Camille Sureau (C)

Institut National de la Transfusion Sanguine, CNR Risques Infectieux Transfusionnels, 75015 Paris, France.

Woottichai Khamduang (W)

Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50100, Thailand.
LUCENT International Collaboration, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50100, Thailand.

Catherine Gaudy-Graffin (C)

Laboratoire de Bactériologie-Virologie-Hygiène, CHRU, Université of Tours, INSERM U1259, 37044 Tours, France.

Classifications MeSH