Rhesus macaque Bcl-6/Bcl-xL B cell immortalization: Discovery of HIV-1 neutralizing antibodies from lymph node.


Journal

Journal of immunological methods
ISSN: 1872-7905
Titre abrégé: J Immunol Methods
Pays: Netherlands
ID NLM: 1305440

Informations de publication

Date de publication:
05 2023
Historique:
received: 03 01 2023
revised: 21 02 2023
accepted: 22 02 2023
medline: 1 5 2023
pubmed: 28 2 2023
entrez: 27 2 2023
Statut: ppublish

Résumé

Many HIV-1 vaccines are designed to elicit neutralizing antibodies, and pre-clinical testing is often carried out in rhesus macaques (RMs). We have therefore adapted a method of B cell immortalization for use with RM B cells. In this system, RM B cells are activated with CD40 ligand and RM IL-21 before transduction with a retroviral vector encoding Bcl-6, Bcl-xL, and green fluorescent protein. Importantly, RM B cells from lymph nodes are more effectively immortalized by this method than B cells from PBMC, a difference not seen in humans. We suggest the discrepancy between these two tissues is due to increased expression of CD40 on RM lymph node B cells. Immortalized RM B cells expand long-term, undergo minimal somatic hypermutation, express surface B cell receptor, and secrete antibodies into culture. This allows for the identification of cells based on antigen specificity and/or functional assays. Here, we show the characterization of this system and its application for the isolation of HIV-1 neutralizing antibodies from a SHIV.CH505-infected animal, both with and without antigen probe. Taken together, we show that Bcl-6/xL immortalization is a valuable and flexible tool for antibody discovery in RMs, but with important distinctions from application of the system in human cells.

Identifiants

pubmed: 36848985
pii: S0022-1759(23)00027-3
doi: 10.1016/j.jim.2023.113445
pii:
doi:

Substances chimiques

HIV Antibodies 0
Antibodies, Neutralizing 0
AIDS Vaccines 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

113445

Informations de copyright

Copyright © 2023. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare no competing interests.

Auteurs

Jakob Samsel (J)

Immunology Laboratory, Vaccine Research Center (VRC), NIAID, NIH, Bethesda, MD, United States of America; Institute for Biomedical Sciences, George Washington University, Washington, D.C., United States of America. Electronic address: jakob.samsel@mail.nih.gov.

Kristin L Boswell (KL)

Immunology Laboratory, Vaccine Research Center (VRC), NIAID, NIH, Bethesda, MD, United States of America.

Timothy Watkins (T)

Immunology Laboratory, Vaccine Research Center (VRC), NIAID, NIH, Bethesda, MD, United States of America.

David R Ambrozak (DR)

Immunology Laboratory, Vaccine Research Center (VRC), NIAID, NIH, Bethesda, MD, United States of America.

Rosemarie Mason (R)

ImmunoTechnology Section, VRC; Humoral Immunology Section, VRC.

Takuya Yamamoto (T)

Immunology Laboratory, Vaccine Research Center (VRC), NIAID, NIH, Bethesda, MD, United States of America.

Sungyoul Ko (S)

ImmunoTechnology Section, VRC.

Yongping Yang (Y)

Structural Biology Section, VRC.

Tongqing Zhou (T)

Structural Biology Section, VRC.

Nicole A Doria-Rose (NA)

Humoral Immunology Section, VRC.

Kathryn E Foulds (KE)

Nonhuman Primate Immunogenicity Core, VRC.

Mario Roederer (M)

ImmunoTechnology Section, VRC.

John R Mascola (JR)

Humoral Immunology Section, VRC.

Peter D Kwong (PD)

Structural Biology Section, VRC.

Lucio Gama (L)

Immunology Laboratory, Vaccine Research Center (VRC), NIAID, NIH, Bethesda, MD, United States of America.

Richard A Koup (RA)

Immunology Laboratory, Vaccine Research Center (VRC), NIAID, NIH, Bethesda, MD, United States of America.

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Classifications MeSH