Evidence map›Paper›PMID 37878666›Full record

ArticlePLoS pathogens2023

High throughput analysis of B cell dynamics and neutralizing antibody development during immunization with a novel clade C HIV-1 envelope.

Rohini Mopuri, Sarah Welbourn, Tysheena Charles, Pooja Ralli-Jain, David Rosales, Samantha Burton, Areeb Aftab, Kirti Karunakaran, Kathryn Pellegrini, William Kilembe and 5 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 39% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 3 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 2 countries.

Rohini MopuriEmory National Primate Research Center, Emory University, Atlanta, Georgia, United States of America.
Sarah WelbournEmory National Primate Research Center, Emory University, Atlanta, Georgia, United States of America.
Tysheena CharlesEmory National Primate Research Center, Emory University, Atlanta, Georgia, United States of America.
Pooja Ralli-JainDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, United States of America.
David RosalesDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, United States of America.
Samantha BurtonEmory National Primate Research Center, Emory University, Atlanta, Georgia, United States of America.
Areeb AftabDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, United States of America.
Kirti KarunakaranEmory National Primate Research Center, Emory University, Atlanta, Georgia, United States of America.
Kathryn PellegriniEmory National Primate Research Center, Emory University, Atlanta, Georgia, United States of America.
William KilembeCenter for Family Health Research in Zambia, Lusaka, Zambia.
Etienne KaritaCenter for Family Health Research, Kigali, Rwanda.
Sandrasegaram GnanakaranTheoretical Division, Los Alamos National Laboratory, Los Alamos, New Mexico, United States of America.
Amit A UpadhyayEmory National Primate Research Center, Emory University, Atlanta, Georgia, United States of America.
Steven E BosingerEmory National Primate Research Center, Emory University, Atlanta, Georgia, United States of America.
Cynthia A DerdeynDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, United States of America.ORCID 0000-0002-1220-513X
Emory University · USUniversity of Washington · USCentre for Infectious Disease Research in Zambia · ZMLos Alamos National Laboratory · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
Virology and Molecular Biomarkers CoreP30AI050409 · NIAID · EMORY UNIVERSITY · PI Ann M Chahroudi, Colleen F Kelley · 2002 to 2026
$74.0M
Role of V1V2 in HIV transmission and pathogenesisR01AI058706 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DERDEYN, CYNTHIA ANN · 2004 to 2016
$6.7M
Using DNA/MVA/protein immunization of rhesus macaques to investigate how the background of the HIV-1 envelope and nature of the protein boost shape the genetic and functional antibody landscape.R01AI128837 · NIAID · EMORY UNIVERSITY · PI BOSINGER, STEVEN EDWARD, DERDEYN, CYNTHIA ANN · 2017 to 2021
$5.9M
Chemical Biology of Infectious Diseases (CBID) Training ProgramT32AI112541 · NIAID · VANDERBILT UNIVERSITY · PI Eric P Skaar · 2015 to 2026
$4.0M
Illumina NovaSeq 6000 High Throughput DNA Sequencer for Emory UniversityS10OD026799 · OD · EMORY UNIVERSITY · PI BOSINGER, STEVEN EDWARD · 2019 to 2019
$985k
NIAID NIH HHS P30 AI050409NIAID NIH HHS R01 AI058706NIAID NIH HHS R01 AI128837NIAID NIH HHS T32 AI112541NIH HHS P51 OD011132NIH HHS S10 OD026799
6 · The paper itself

Abstract

A protective HIV-1 vaccine has been hampered by a limited understanding of how B cells acquire neutralizing activity. Our previous vaccines expressing two different HIV-1 envelopes elicited robust antigen specific serum IgG titers in 20 rhesus macaques; yet serum from only two animals neutralized the autologous virus. Here, we used high throughput immunoglobulin receptor and single cell RNA sequencing to characterize the overall expansion, recall, and maturation of antigen specific B cells longitudinally over 90 weeks. Diversification and expansion of many B cell clonotypes occurred broadly in the absence of serum neutralization. However, in one animal that developed neutralization, two neutralizing B cell clonotypes arose from the same immunoglobulin germline and were tracked longitudinally. Early antibody variants with high identity to germline neutralized the autologous virus while later variants acquired somatic hypermutation and increased neutralization potency. The early engagement of precursors capable of neutralization with little to no SHM followed by prolonged affinity maturation allowed the two neutralizing lineages to successfully persist despite many other antigen specific B cells. The findings provide new insight into B cells responding to HIV-1 envelope during heterologous prime and boost immunization in rhesus macaques and the development of selected autologous neutralizing antibody lineages.

Indexed as

AIDS VaccinesHIV-1HIV InfectionsHIV SeropositivityAnimalsAntibodies, Neutralizingenv Gene Products, Human Immunodeficiency VirusHIV AntibodiesImmunizationMacaca mulattaAIDS VaccinesAntibodies, Neutralizingenv Gene Products, Human Immunodeficiency VirusHIV Antibodies

Identifiers

PMID37878666
PMCPMC10627474
OpenAlexW4387934801

What OpenQuestion holds

Textmetadata
LicenceCC0
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.