Evidence map›Paper›PMID 27852851›Full record

ArticleJournal of virology2017

Identification of Human Anti-HIV gp160 Monoclonal Antibodies That Make Effective Immunotoxins.

Seth H Pincus, Kejing Song, Grace A Maresh, Dean H Hamer, Dimiter S Dimitrov, Weizao Chen, Mei-Yun Zhang, Victor F Ghetie, Po-Ying Chan-Hui, James E Robinson and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2017. 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
1.3field-weighted citation impact, top 19% 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

21 citing papers in PubMed, 27 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

11 authors at 6 institutions in 1 country.

Seth H PincusResearch Institute for Children, Children's Hospital, New Orleans, Louisiana, USA spincu@lsuhsc.edu.
Kejing SongResearch Institute for Children, Children's Hospital, New Orleans, Louisiana, USA.
Grace A MareshResearch Institute for Children, Children's Hospital, New Orleans, Louisiana, USA.
Dean H HamerLaboratory of Biochemistry, Center for Cancer Research, NCI, Bethesda, Maryland, USA.
Dimiter S DimitrovCancer and Inflammation Program, Center for Cancer Research, NCI, Frederick, Maryland, USA.
Weizao ChenCancer and Inflammation Program, Center for Cancer Research, NCI, Frederick, Maryland, USA.
Mei-Yun ZhangCancer and Inflammation Program, Center for Cancer Research, NCI, Frederick, Maryland, USA.
Victor F GhetieDepartments of Immunology and Microbiology, UT Southwestern Medical Center, Dallas, Texas, USA.
Po-Ying Chan-HuiTheraclone Sciences, Seattle, Washington, USA.
James E RobinsonDepartment of Pediatrics, Tulane University School of Medicine, New Orleans, Louisiana, USA.
Ellen S VitettaDepartments of Immunology and Microbiology, UT Southwestern Medical Center, Dallas, Texas, USA.
Center for Cancer Research · USChildren's Hospital of New Orleans · USSouthwestern Medical CenterSouthwestern Medical Center · USTheraclone Sciences (United States) · USTulane University · US

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Leigh Lamonica · 2012 to 2026
$69.1M
Neutralizing Antibody Induction by Centralized GenesP01AI061734 · NIAID · DUKE UNIVERSITY · PI LIAO, HUA-XIN · 2005 to 2009
$11.7M
Antibody-based therapeutics and vaccines against AIDSZIABC011155 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DIMITROV, DIMITER S · 2009 to 2017
$2.6M
Furin Inhibition in HIV DiseaseR21AI058714 · NIAID · LOUISIANA STATE UNIV HSC NEW ORLEANS · PI PINCUS, SETH H. · 2004 to 2006
$554k
IN VIVO ACTIVITY OF ANTIGP41 IMMUNOTOXINSR01CA074690 · NCI · MONTANA STATE UNIVERSITY (BOZEMAN) · PI PINCUS, SETH H. · 1998 to 1999
–
NCI NIH HHS R01 CA074690NIAID NIH HHS P01 AI061734NIAID NIH HHS R21 AI058714NIGMS NIH HHS U54 GM104940
6 · The paper itself

Abstract

The envelope (Env) glycoprotein of HIV is the only intact viral protein expressed on the surface of both virions and infected cells. Env is the target of neutralizing antibodies (Abs) and has been the subject of intense study in efforts to produce HIV vaccines. Therapeutic anti-Env Abs can also exert antiviral effects via Fc-mediated effector mechanisms or as cytotoxic immunoconjugates, such as immunotoxins (ITs). In the course of screening monoclonal antibodies (MAbs) for their ability to deliver cytotoxic agents to infected or Env-transfected cells, we noted disparities in their functional activities. Different MAbs showed diverse functions that did not correlate with each other. For example, MAbs against the external loop region of gp41 made the most effective ITs against infected cells but did not neutralize virus and bound only moderately to the same cells that they killed so effectively when they were used in ITs. There were also differences in IT-mediated killing among transfected and infected cell lines that were unrelated to the binding of the MAb to the target cells. Our studies of a well-characterized antigen demonstrate that MAbs against different epitopes have different functional activities and that the binding of one MAb can influence the interaction of other MAbs that bind elsewhere on the antigen. These results have implications for the use of MAbs and ITs to kill HIV-infected cells and eradicate persistent reservoirs of HIV infection. IMPORTANCE: There is increased interest in using antibodies to treat and cure HIV infection. Antibodies can neutralize free virus and kill cells already carrying the virus. The virus envelope (Env) is the only HIV protein expressed on the surfaces of virions and infected cells. In this study, we examined a panel of human anti-Env antibodies for their ability to deliver cell-killing toxins to HIV-infected cells and to perform other antiviral functions. The ability of an antibody to make an effective immunotoxin could not be predicted from its other functional characteristics, such as its neutralizing activity. Anti-HIV immunotoxins could be used to eliminate virus reservoirs that persist despite effective antiretroviral therapy.

Indexed as

Antibodies, MonoclonalCD4 AntigensCell LineEpitopesHIV-1HIV AntibodiesHIV Envelope Protein gp160HIV InfectionsHumansImmunotoxinsNeutralization TestsProtein BindingProtein MultimerizationAntibodies, MonoclonalCD4 AntigensEpitopesHIV AntibodiesHIV Envelope Protein gp160Immunotoxinsepitopegp160HIV envelopeimmunotoxinmonoclonal antibody

Identifiers

PMID27852851
PMCPMC5244328
OpenAlexW2550738779

What OpenQuestion holds

Textmetadata
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.