Evidence map›Paper›PMID 25398324›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Antibody to the gp120 V1/V2 loops and CD4+ and CD8+ T cell responses in protection from SIVmac251 vaginal acquisition and persistent viremia.

Shari N Gordon, Melvin N Doster, Rhonda C Kines, Brandon F Keele, Egidio Brocca-Cofano, Yongjun Guan, Poonam Pegu, Namal P M Liyanage, Monica Vaccari, Nicolas Cuburu and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

29 citing papers in PubMed, 37 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

22 authors at 8 institutions in 2 countries.

Shari N GordonAnimal Models and Retroviral Vaccines Section, National Cancer Institute, Bethesda, MD 20892;
Melvin N DosterAnimal Models and Retroviral Vaccines Section, National Cancer Institute, Bethesda, MD 20892;
Rhonda C KinesLaboratory of Cellular Oncology, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20982;
Brandon F KeeleAIDS and Cancer Virus Program, Leidos Biomedical Research, Frederick National Laboratory for Cancer Research, Frederick, MD 21702;
Egidio Brocca-CofanoVaccine Branch, National Cancer Institute, Bethesda, MD 20892;
Yongjun GuanDivision of Basic Science and Vaccine Research, Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD 21201;
Poonam PeguAnimal Models and Retroviral Vaccines Section, National Cancer Institute, Bethesda, MD 20892;
Namal P M LiyanageAnimal Models and Retroviral Vaccines Section, National Cancer Institute, Bethesda, MD 20892;
Monica VaccariAnimal Models and Retroviral Vaccines Section, National Cancer Institute, Bethesda, MD 20892;
Nicolas CuburuLaboratory of Cellular Oncology, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20982;
Christopher B BuckLaboratory of Cellular Oncology, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20982;
Guido FerrariDepartment of Surgery, Duke University Medical Center, Durham, NC 27710;
David MontefioriDepartment of Surgery, Duke University Medical Center, Durham, NC 27710;
Michael PiatakAIDS and Cancer Virus Program, Leidos Biomedical Research, Frederick National Laboratory for Cancer Research, Frederick, MD 21702;
Jeffrey D LifsonAIDS and Cancer Virus Program, Leidos Biomedical Research, Frederick National Laboratory for Cancer Research, Frederick, MD 21702;
Anastasia M XenophontosAnimal Models and Retroviral Vaccines Section, National Cancer Institute, Bethesda, MD 20892;
David VenzonBiostatistics and Data Management Section, National Cancer Institute, Bethesda, MD 20892; and.
Marjorie Robert-GuroffVaccine Branch, National Cancer Institute, Bethesda, MD 20892;
Barney S GrahamVaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892.
Douglas R LowyLaboratory of Cellular Oncology, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20982;
John T SchillerLaboratory of Cellular Oncology, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20982;
Genoveffa FranchiniAnimal Models and Retroviral Vaccines Section, National Cancer Institute, Bethesda, MD 20892; franchig@mail.nih.gov.
National Cancer Institute · USCenter for Cancer Research · USDuke University Hospital · USFrederick National Laboratory for Cancer Research · USLeidos (United States) · USNational Cancer Institute · UANational Institute of Allergy and Infectious Diseases · USUniversity of Maryland, Baltimore · US

Funding

Development of a Vaccine for HIVAIDS: Cellular ImmunityZIABC011062 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ROBERT-GUROFF, MARJORIE · 2009 to 2020
$12.8M
Vaccine Modalities to Prevent HIV-I InfectionZ01BC005688 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FRANCHINI, GENOVEFFA · 1996 to 2008
$4.2M
CCR NIH HHS HHSN261200800001CIntramural NIH HHS Z01 BC005688NCI NIH HHS HHSN261200800001EPHS HHS HHSN266200400088C
6 · The paper itself

Abstract

The human papillomavirus pseudovirions (HPV-PsVs) approach is an effective gene-delivery system that can prime or boost an immune response in the vaginal tract of nonhuman primates and mice. Intravaginal vaccination with HPV-PsVs expressing SIV genes, combined with an i.m. gp120 protein injection, induced humoral and cellular SIV-specific responses in macaques. Priming systemic immune responses with i.m. immunization with ALVAC-SIV vaccines, followed by intravaginal HPV-PsV-SIV/gp120 boosting, expanded and/or recruited T cells in the female genital tract. Using a stringent repeated low-dose intravaginal challenge with the highly pathogenic SIVmac251, we show that although these regimens did not demonstrate significant protection from virus acquisition, they provided control of viremia in a number of animals. High-avidity Ab responses to the envelope gp120 V1/V2 region correlated with delayed SIVmac251 acquisition, whereas virus levels in mucosal tissues were inversely correlated with antienvelope CD4(+) T cell responses. CD8(+) T cell depletion in animals with controlled viremia caused an increase in tissue virus load in some animals, suggesting a role for CD8(+) T cells in virus control. This study highlights the importance of CD8(+) cells and antienvelope CD4(+) T cells in curtailing virus replication and antienvelope V1/V2 Abs in preventing SIVmac251 acquisition.

Indexed as

AlphapapillomavirusAnimalsAntibodies, ViralAntibody SpecificityCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDisease Models, AnimalFemaleGenetic VectorsLymphocyte DepletionMacaca mulattaMolecular Sequence DataMucous MembranePeptide FragmentsSAIDS VaccinesSimian Acquired Immunodeficiency SyndromeAntibodies, ViralPeptide FragmentsSAIDS VaccinesVaccines, DNAViral Envelope Proteins

Identifiers

PMID25398324
PMCPMC4335709
OpenAlexW2116835799

What OpenQuestion holds

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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.