Evidence map›Paper›PMID 27591322›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

Boosting of ALVAC-SIV Vaccine-Primed Macaques with the CD4-SIVgp120 Fusion Protein Elicits Antibodies to V2 Associated with a Decreased Risk of SIVmac251 Acquisition.

Shari N Gordon, Namal P M Liyanage, Melvin N Doster, Monica Vaccari, Diego A Vargas-Inchaustegui, Poonam Pegu, Luca Schifanella, Xiaoying Shen, Georgia D Tomaras, Mangala Rao and 17 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 36 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

27 authors at 8 institutions in 1 country.

Shari N GordonAnimal Models and Vaccine Section, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892;ORCID 0000-0001-6715-7334
Namal P M LiyanageAnimal Models and Vaccine Section, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892;ORCID 0000-0001-7362-3282
Melvin N DosterAnimal Models and Vaccine Section, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892;
Monica VaccariAnimal Models and Vaccine Section, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892;
Diego A Vargas-InchausteguiImmune Biology of Retroviral Infection Section, Vaccine Branch, National Cancer Institute, Bethesda, MD 20892;ORCID 0000-0001-7405-9572
Poonam PeguAnimal Models and Vaccine Section, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892;ORCID 0000-0001-7926-3118
Luca SchifanellaAnimal Models and Vaccine Section, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892;
Xiaoying ShenDuke University Medical Center, Durham, NC 27710;
Georgia D TomarasDuke University Medical Center, Durham, NC 27710;ORCID 0000-0001-8076-1931
Mangala RaoU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD 20910;ORCID 0000-0001-9553-4969
Erik A BillingsU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD 20910;ORCID 0000-0002-8963-0484
Jennifer SchwartzProfectus BioSciences Inc., Baltimore, MD 21224;ORCID 0000-0001-8239-8857
Ilia PradoProfectus BioSciences Inc., Baltimore, MD 21224;
Kathryn BobbProfectus BioSciences Inc., Baltimore, MD 21224;
Wenlei ZhangProfectus BioSciences Inc., Baltimore, MD 21224;
David C MontefioriDuke University Medical Center, Durham, NC 27710;ORCID 0000-0003-0856-6319
Kathryn E FouldsVaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892;
Guido FerrariDuke University Medical Center, Durham, NC 27710;ORCID 0000-0001-7747-3349
Marjorie Robert-GuroffImmune Biology of Retroviral Infection Section, Vaccine Branch, National Cancer Institute, Bethesda, MD 20892;
Mario RoedererVaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892;ORCID 0000-0001-7448-7040
Tran B PhanDivision of Infectious Diseases, Department of Medicine, University of California, Irvine School of Medicine, Irvine, CA 92868;
Donald N ForthalDivision of Infectious Diseases, Department of Medicine, University of California, Irvine School of Medicine, Irvine, CA 92868;
Donald M StableinThe Emmes Corporation, Rockville, MD 20850;
Sanjay PhogatSanofi Pasteur, Swiftwater, PA 18370; and.
David J VenzonBiostatistics and Data Management Section, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.ORCID 0000-0002-8990-158X
Timothy FoutsProfectus BioSciences Inc., Baltimore, MD 21224;ORCID 0000-0002-2429-2859
Genoveffa FranchiniAnimal Models and Vaccine Section, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892; franchig@mail.nih.gov.ORCID 0000-0001-5171-9849
National Institutes of Health · USProfectus Biosciences (United States) · USDuke Medical Center · USNational Cancer Institute · USUniversity of California, Irvine · USWalter Reed Army Institute of Research · USEmmes (United States) · USSanofi (United States) · US

Funding

Vaccine Modalities to Prevent HIV-I InfectionZ01BC005688 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FRANCHINI, GENOVEFFA · 1996 to 2008
$4.2M
Intramural NIH HHS Z01 BC005688
6 · The paper itself

Abstract

The recombinant ALVAC vaccine coupled with the monomeric gp120/alum protein have decreased the risk of HIV and SIV acquisition. Ab responses to the V1/V2 regions have correlated with a decreased risk of virus acquisition in both humans and macaques. We hypothesized that the breadth and functional profile of Abs induced by an ALVAC/envelope protein regimen could be improved by substituting the monomeric gp120 boost, with the full-length single-chain (FLSC) protein. FLSC is a CD4-gp120 fusion immunogen that exposes cryptic gp120 epitopes to the immune system. We compared the immunogenicity and relative efficiency of an ALVAC-SIV vaccine boosted either with bivalent FLSC proteins or with monomeric gp120 in alum. FLSC was superior to monomeric gp120 in directing Abs to the C3 α2 helix, the V5 loop, and the V3 region that contains the putative CCR5 binding site. In addition, FLSC boosting elicited significantly higher binding Abs to V2 and increased both the Ab-dependent cellular cytotoxicity activity and the breadth of neutralizing Abs. However, the FLSC vaccine regimen demonstrated only a trend in vaccine efficacy, whereas the monomeric gp120 regimen significantly decreased the risk of SIVmac251 acquisition. In both vaccine regimens, anti-V2 Abs correlated with a decreased risk of virus acquisition but differed with regard to systemic or mucosal origin. In the FLSC regimen, serum Abs to V2 correlated, whereas in the monomeric gp120 regimen, V2 Abs in rectal secretions, the site of viral challenge, were associated with efficacy.

Indexed as

AnimalsAntibodies, ViralCD4 AntigensCell LineGene Products, envMacaca mulattaSAIDS VaccinesSimian Acquired Immunodeficiency SyndromeViral VaccinesALVAC vaccineAntibodies, ViralCD4 AntigensGene Products, envSAIDS VaccinesViral Vaccines

Identifiers

PMID27591322
PMCPMC5026031
OpenAlexW2513999863

What OpenQuestion holds

Textmetadata
LicenceTDM
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.