Antibody dependent cell cytotoxicity is maintained by the unmutated common ancestor of 6F5, a Gp41 conformational epitope targeting antibody that utilizes heavy chain VH1-2.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
29 07 2022
Historique:
received: 31 12 2021
revised: 24 05 2022
accepted: 28 05 2022
pubmed: 11 6 2022
medline: 22 6 2022
entrez: 10 6 2022
Statut: ppublish

Résumé

In studies on monoclonal IgG antibodies (mAbs) from long-term non-progressors (LTNPs), our laboratory has previously described highly mutated Abs against a complex conformational epitope with contributions from both gp41 the N terminal and C terminal heptad repeat helices. Despite using the VH1-2 gene segment, known to contribute to some of the broadest neutralizing Abs against HIV, members of these Abs, termed group 76C Abs, did not exhibit broad neutralization. Because of the high number of mutations and use of VH1-2, our goal was to characterize the non-neutralizing functions of Abs of group 76C, to assess if targeting of the epitope correlates with LTNP, and to assess the maturation of these Abs by comparison to their predicted common ancestor. Serum competition assays showed group 76C Abs were enriched in LTNPs, in comparison to VRC-01. Specific group 76C clones 6F5 and 6F11, expressed as recombinant Abs, both have robust ADCC activity, despite their sequence disparity. Sequence analysis predicted the common ancestor of this clonal group would utilize the germline non-mutated variable gene. We produced a recombinant ancestor Ab (76Canc) with a heavy chain utilizing the germline variable gene sequence paired to the 6F5 light chain. Competition with group 76C recombinant Ab 6F5 confirms 76Canc binds HIV envelope constructs near the original group C epitope. 76Canc demonstrates comparable ADCC to 6F5 and 6F11 when using gp41 constructs of both clade B and clade C. The functional capability of Abs utilizing germline VH1-2 has implications for disease control and vaccine development.

Identifiants

pubmed: 35688727
pii: S0264-410X(22)00719-8
doi: 10.1016/j.vaccine.2022.05.083
pii:
doi:

Substances chimiques

Antibodies, Monoclonal 0
Antibodies, Neutralizing 0
Epitopes 0
HIV Antibodies 0
HIV Envelope Protein gp41 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

4174-4181

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI125119
Pays : United States

Informations de copyright

Copyright © 2022. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Mark Daniel Hicar reports financial support was provided by National Institutes of Health.

Auteurs

Brian H Wrotniak (BH)

Department of Pediatrics, University at Buffalo, Buffalo, NY, USA.

Meghan Garrett (M)

Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

Sarah Baron (S)

Department of Pediatrics, University at Buffalo, Buffalo, NY, USA.

Hakimuddin Sojar (H)

Department of Pediatrics, University at Buffalo, Buffalo, NY, USA.

Alyssa Shon (A)

Department of Medicine, University at Buffalo, Buffalo, NY, USA.

Elizabeth Asiago-Reddy (E)

Department of Medicine, SUNY Upstate, Syracuse, NY, USA.

Jessica Yager (J)

Department of Medicine, SUNY Downstate, New York City, NY, USA.

Spyros Kalams (S)

Department of Internal Medicine, Vanderbilt University, Nashville, TN, USA.

Michael Croix (M)

Department of Pediatrics, University at Buffalo, Buffalo, NY, USA.

Mark D Hicar (MD)

Department of Pediatrics, University at Buffalo, Buffalo, NY, USA. Electronic address: markhica@buffalo.edu.

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Classifications MeSH