Evidence map›Paper›PMID 30842326›Full record

ArticleJournal of virology2019

Bridging Vaccine-Induced HIV-1 Neutralizing and Effector Antibody Responses in Rabbit and Rhesus Macaque Animal Models.

Justin Pollara, Dorothy I Jones, Tori Huffman, R Whitney Edwards, Maria Dennis, Shuk Hang Li, Shalini Jha, Derrick Goodman, Amit Kumar, Celia C LaBranche and 7 more

Abstract read
In one paragraph

Article in Journal of virology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

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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

17 authors.

Justin PollaraDepartment of Surgery, Duke University School of Medicine, Durham, North Carolina, USA justin.pollara@duke.edu.
Dorothy I JonesDepartment of Pathology, Duke University School of Medicine, Durham, North Carolina, USA.
Tori HuffmanDepartment of Surgery, Duke University School of Medicine, Durham, North Carolina, USA.
R Whitney EdwardsDepartment of Surgery, Duke University School of Medicine, Durham, North Carolina, USA.
Maria DennisHuman Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
Shuk Hang LiHuman Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
Shalini JhaDepartment of Surgery, Duke University School of Medicine, Durham, North Carolina, USA.
Derrick GoodmanHuman Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
Amit KumarHuman Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
Celia C LaBrancheDepartment of Surgery, Duke University School of Medicine, Durham, North Carolina, USA.ORCID 0000-0002-6653-6655
David C MontefioriDepartment of Surgery, Duke University School of Medicine, Durham, North Carolina, USA.
Genevieve G FoudaHuman Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.
Thomas J HopeDepartment of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID 0000-0001-7183-8319
Georgia D TomarasDepartment of Surgery, Duke University School of Medicine, Durham, North Carolina, USA.ORCID 0000-0001-8076-1931
Herman F StaatsHuman Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.ORCID 0000-0003-1039-1087
Guido Ferrari *Department of Surgery, Duke University School of Medicine, Durham, North Carolina, USA.
Sallie R Permar *Human Vaccine Institute, Duke University School of Medicine, Durham, North Carolina, USA.

Funding

Social and Behavioral Sciences CoreP30AI064518 · NIAID · DUKE UNIVERSITY · PI Nwora Lance Okeke · 2005 to 2026
$50.5M
Project 2: RNA vaccination in early life to induce potent and broad HIV Env-specific antibody responsesP01AI117915 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI DE PARIS, KRISTINA, PERMAR, SALLIE R. · 2015 to 2024
$21.2M
Physical Resources CoreP01AI120756 · NIAID · DUKE UNIVERSITY · PI TOMARAS, GEORGIA DORIS · 2016 to 2020
$17.1M
Mucosal vaccination to protect against HIV-1 infection at mucosal sitesR01AI102747 · NIAID · DUKE UNIVERSITY · PI STAATS, HERMAN F · 2012 to 2015
$2.3M
Combined Hepatitis B and HIV-1 envelope vaccination to augment T cell help via linked recognition of unrelated antigensK01OD024877 · OD · DUKE UNIVERSITY · PI POLLARA, JUSTIN JOSEPH · 2017 to 2019
$1.0M
NIAID NIH HHS P01 AI117915NIAID NIH HHS P01 AI120756NIAID NIH HHS P30 AI064518NIAID NIH HHS R01 AI102747NIH HHS K01 OD024877
6 · The paper itself

Abstract

Studies in animal models are essential prerequisites for clinical trials of candidate HIV vaccines. Small animals, such as rabbits, are used to evaluate promising strategies prior to further immunogenicity and efficacy testing in nonhuman primates. Our goal was to determine how HIV-specific vaccine-elicited antibody responses, epitope specificity, and Fc-mediated functions in the rabbit model can predict those in the rhesus macaque (RM) model. Detailed comparisons of the HIV-1-specific IgG response were performed on serum from rabbits and RM given identical modified vaccinia virus Ankara-prime/gp120-boost immunization regimens. We found that vaccine-induced neutralizing antibody, gp120-binding antibody levels and immunodominant specificities, antibody-dependent cellular phagocytosis of HIV-1 virions, and antibody-dependent cellular cytotoxicity (ADCC) responses against gp120-coated target cells were similar in rabbits and RM. However, we also identified characteristics of humoral immunity that differed across species. ADCC against HIV-infected target cells was elicited in rabbits but not in RM, and we observed differences among subdominantly targeted epitopes. Human Fc receptor binding assays and analysis of antibody-cell interactions indicated that rabbit vaccine-induced antibodies effectively recruited and activated human natural killer cells, while vaccine-elicited RM antibodies were unable to activate either human or RM NK cells. Thus, our data demonstrate that both Fc-independent and Fc-dependent functions of rabbit antibodies can be measured with commonly used

Indexed as

AIDS VaccinesAnimalsAntibodies, NeutralizingAntibody FormationB-Lymphocyte SubsetsDisease Models, AnimalEpitopesHIV-1HIV AntibodiesHIV Envelope Protein gp120HIV InfectionsHIV SeropositivityHumansMacaca mulattaRabbitsSpecies SpecificityAIDS VaccinesAntibodies, NeutralizingEpitopesHIV AntibodiesHIV Envelope Protein gp120ADCCADCPantibody Fc functionsHIV-1 vaccinesrabbit modelrhesus macaques

Identifiers

PMID30842326
PMCPMC6498063

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Registered trials

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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.