» Articles » PMID: 30876875

Longitudinal Analysis Reveals Early Development of Three MPER-Directed Neutralizing Antibody Lineages from an HIV-1-Infected Individual

Abstract

Lineage-based vaccine design is an attractive approach for eliciting broadly neutralizing antibodies (bNAbs) against HIV-1. However, most bNAb lineages studied to date have features indicative of unusual recombination and/or development. From an individual in the prospective RV217 cohort, we identified three lineages of bNAbs targeting the membrane-proximal external region (MPER) of the HIV-1 envelope. Antibodies RV217-VRC42.01, -VRC43.01, and -VRC46.01 used distinct modes of recognition and neutralized 96%, 62%, and 30%, respectively, of a 208-strain virus panel. All three lineages had modest levels of somatic hypermutation and normal antibody-loop lengths and were initiated by the founder virus MPER. The broadest lineage, VRC42, was similar to the known bNAb 4E10. A multimeric immunogen based on the founder MPER activated B cells bearing the unmutated common ancestor of VRC42, with modest maturation of early VRC42 intermediates imparting neutralization breadth. These features suggest that VRC42 may be a promising template for lineage-based vaccine design.

Citing Articles

Progress and Challenges in HIV-1 Vaccine Research: A Comprehensive Overview.

Boomgarden A, Upadhyay C Vaccines (Basel). 2025; 13(2).

PMID: 40006695 PMC: 11860913. DOI: 10.3390/vaccines13020148.


Differences in neutralizing antibody sensitivities and envelope characteristics indicate distinct antigenic properties of Nigerian HIV-1 subtype G and CRF02_AG.

Wieczorek L, Chang D, Sanders-Buell E, Zemil M, Martinez E, Schoen J Virol J. 2024; 21(1):148.

PMID: 38951814 PMC: 11218331. DOI: 10.1186/s12985-024-02394-y.


RAIN: machine learning-based identification for HIV-1 bNAbs.

Foglierini M, Nortier P, Schelling R, Winiger R, Jacquet P, ODell S Nat Commun. 2024; 15(1):5339.

PMID: 38914562 PMC: 11196741. DOI: 10.1038/s41467-024-49676-1.


RAIN: a Machine Learning-based identification for HIV-1 bNAbs.

Perez L, Foglierini M Res Sq. 2024; .

PMID: 38903123 PMC: 11188109. DOI: 10.21203/rs.3.rs-4023897/v1.


Affinity gaps among B cells in germinal centers drive the selection of MPER precursors.

Ray R, Schiffner T, Wang X, Yan Y, Rantalainen K, Lee C Nat Immunol. 2024; 25(6):1083-1096.

PMID: 38816616 PMC: 11147770. DOI: 10.1038/s41590-024-01844-7.


References
1.
Kwong P, Mascola J . Human antibodies that neutralize HIV-1: identification, structures, and B cell ontogenies. Immunity. 2012; 37(3):412-25. PMC: 4706166. DOI: 10.1016/j.immuni.2012.08.012. View

2.
Weaver G, Villar R, Kanekiyo M, Nabel G, Mascola J, Lingwood D . In vitro reconstitution of B cell receptor-antigen interactions to evaluate potential vaccine candidates. Nat Protoc. 2016; 11(2):193-213. PMC: 6956844. DOI: 10.1038/nprot.2016.009. View

3.
Scherer E, Smith R, Simonich C, Niyonzima N, Carter J, Galloway D . Characteristics of memory B cells elicited by a highly efficacious HPV vaccine in subjects with no pre-existing immunity. PLoS Pathog. 2014; 10(10):e1004461. PMC: 4199765. DOI: 10.1371/journal.ppat.1004461. View

4.
Langer G, Cohen S, Lamzin V, Perrakis A . Automated macromolecular model building for X-ray crystallography using ARP/wARP version 7. Nat Protoc. 2008; 3(7):1171-9. PMC: 2582149. DOI: 10.1038/nprot.2008.91. View

5.
Moody M, Pedroza-Pacheco I, Vandergrift N, Chui C, Lloyd K, Parks R . Immune perturbations in HIV-1-infected individuals who make broadly neutralizing antibodies. Sci Immunol. 2017; 1(1):aag0851. PMC: 5589960. DOI: 10.1126/sciimmunol.aag0851. View