Evidence map›Paper›PMID 29321320›Full record

ArticleJournal of virology2018

HIV-1-Specific IgA Monoclonal Antibodies from an HIV-1 Vaccinee Mediate Galactosylceramide Blocking and Phagocytosis.

Saintedym Wills, Kwan-Ki Hwang, Pinghuang Liu, S Moses Dennison, Matthew Zirui Tay, Xiaoying Shen, Justin Pollara, Judith T Lucas, Robert Parks, Supachai Rerks-Ngarm and 17 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of virology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

30 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

27 authors at 9 institutions in 3 countries.

Saintedym Wills *Duke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0003-2379-8679
Kwan-Ki Hwang *Duke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Pinghuang Liu *Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, Heilongjiang, China.
S Moses DennisonDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Matthew Zirui TayDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Xiaoying ShenDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Justin PollaraDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Judith T LucasDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Robert ParksDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Supachai Rerks-NgarmDepartment of Disease Control, Ministry of Public Health, Nonthaburi, Thailand.
Punnee PitisuttithumVaccine Trial Center, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Sorachai NitayapanRoyal Thai Army, Armed Forces Research Institute of Medical Sciences, Bangkok, Thailand.
Jaranit KaewkungwalCenter of Excellence for Biomedical and Public Health Informatics, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Rasmi ThomasU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Jerome H KimU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Nelson L MichaelU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Merlin L RobbU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Mike McRavenDepartment of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
David C MontefioriDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Thomas J HopeDepartment of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Hua-Xin LiaoDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
M Anthony MoodyDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Guido FerrariDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Barton F HaynesDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
S Munir AlamDuke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Mattia Bonsignori *Duke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA.
Georgia D Tomaras *Duke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA gdt@duke.edu.ORCID https://orcid.org/0000-0001-8076-1931
Duke Medical Center · USDuke University · USHenry M. Jackson Foundation · USMahidol University · THNorthwestern University · USWalter Reed Army Institute of Research · USArmed Forces Research Institute of Medical Science · THChinese Academy of Agricultural Sciences · CNMinistry of Public Health · TH

Funding

LC: HIV Vaccine Trials NetworkUM1AI068618 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Margaret Juliana McElrath · 2011 to 2026
$483.6M
Social and Behavioral Sciences CoreP30AI064518 · NIAID · DUKE UNIVERSITY · PI GEORGIA Doris TOMARAS · 2005 to 2026
$50.5M
Physical Resources CoreP01AI120756 · NIAID · DUKE UNIVERSITY · PI TOMARAS, GEORGIA DORIS · 2016 to 2020
$17.1M
Basic Immunology Training ProgramT32AI052077 · NIAID · DUKE UNIVERSITY · PI KRANGEL, MICHAEL S · 2002 to 2024
$4.2M
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
The duality of vaccine elicited HIV specific-IgA antibodies: Providing protection or diminishing protectionF31AI122967 · NIAID · DUKE UNIVERSITY · PI WILLS, SAINTEDYM · 2016 to 2017
$69k
NIAID NIH HHS F31 AI122967NIAID NIH HHS P01 AI120756NIAID NIH HHS P30 AI064518NIAID NIH HHS T32 AI052077NIAID NIH HHS UM1 AI068618NIH HHS K01 OD024877
6 · The paper itself

Abstract

Vaccine-elicited humoral immune responses comprise an array of antibody forms and specificities, with only a fraction contributing to protective host immunity. Elucidation of antibody effector functions responsible for protective immunity against human immunodeficiency virus type 1 (HIV-1) acquisition is a major goal for the HIV-1 vaccine field. Immunoglobulin A (IgA) is an important part of the host defense against pathogens; however, little is known about the role of vaccine-elicited IgA and its capacity to mediate antiviral functions. To identify the antiviral functions of HIV-1-specific IgA elicited by vaccination, we cloned HIV-1 envelope-specific IgA monoclonal antibodies (MAbs) by memory B cell cultures from peripheral blood mononuclear cells from an RV144 vaccinee and produced two IgA clonal cell lines (HG129 and HG130) producing native, nonrecombinant IgA MAbs. The HG129 and HG130 MAbs mediated phagocytosis by monocytes, and HG129 blocked HIV-1 Env glycoprotein binding to galactosylceramide, an alternative HIV-1 receptor. These findings elucidate potential antiviral functions of vaccine-elicited HIV-1 envelope-specific IgA that may act to block HIV-1 acquisition at the portal of entry by preventing HIV-1 binding to galactosylceramide and mediating antibody Fc receptor-mediated virion phagocytosis. Furthermore, these findings highlight the complex and diverse interactions of vaccine-elicited IgA with pathogens that depend on IgA fine specificity and form (e.g., multimeric or monomeric) in the systemic circulation and mucosal compartments.

Indexed as

AIDS VaccinesAntibodies, BlockingAntibodies, MonoclonalCell LineGalactosylceramidesHIV-1HIV AntibodiesHumansImmunoglobulin APhagocytosisAIDS VaccinesAntibodies, BlockingAntibodies, MonoclonalGalactosylceramidesHIV AntibodiesImmunoglobulin AB cellHIV-1IgAmonoclonal antibodiesnonneutralizing antibodiesvaccinevaccines

Identifiers

PMID29321320
PMCPMC5972890
OpenAlexW2784140966

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.