Evidence map›Paper›PMID 18066039›Full record

ReviewNature biotechnology2007

The growth and potential of human antiviral monoclonal antibody therapeutics.

Wayne A Marasco, Jianhua Sui

Open access · bronzeAbstract readReview
In one paragraph

Review in Nature biotechnology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 146 papers.

0numbers the graph read from it
0cells of the map it votes in
146citing papers in PubMed
11.4field-weighted citation impact, top 1% 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

146 citing papers in PubMed, 279 citations in OpenAlex.

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  20. Dengue: Update on Clinically Relevant Therapeutic Strategies and Vaccines.Current treatment options in infectious diseases · 2023
    Review

86 more citing papers are in PubMed but not listed here.

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

2 authors at 2 institutions in 1 country.

Wayne A MarascoDepartment of Cancer Immunology & AIDS, Dana-Farber Cancer Institute and Department of Medicine, Harvard Medical School 44, Binney Street, Boston, Massachusetts 02115, USA. wayne_marasco@dfci.harvard.edu
Jianhua Sui
Dana-Farber/Harvard Cancer Center · USHarvard University · US

Funding

Human Mab Cocktails to Prevent & Treat H5N1 Avian InfluenzaU01AI074518 · NIAID · DANA-FARBER CANCER INST · PI MARASCO, WAYNE A. · 2007 to 2011
$7.2M
Immunotherapeutics for Treatment of Flavivirus InfectionU01AI070343 · NIAID · YALE UNIVERSITY · PI FIKRIG, EROL · 2006 to 2010
$6.6M
Human Antibodies and Targeted Vaccines Against SARS-CoVU01AI061318 · NIAID · DANA-FARBER CANCER INSTITUTE · PI MARASCO, WAYNE A. · 2004 to 2008
$3.6M
Human Anti-Macaque CCR5 Mabs for Passive ImmunotherapyR01AI052829 · NIAID · DANA-FARBER CANCER INSTITUTE · PI MARASCO, WAYNE A. · 2003 to 2007
$1.9M
Studies of CCR5 Conformational Heterogeneity &HIV EntryR01AI060456 · NIAID · DANA-FARBER CANCER INSTITUTE · PI MARASCO, WAYNE A. · 2004 to 2008
$1.9M
NIAID NIH HHS AI060456NIAID NIH HHS AI061318NIAID NIH HHS AI070343NIAID NIH HHS AI074518NIAID NIH HHS AI52829NIAID NIH HHS R01 AI052829NIAID NIH HHS R01 AI060456NIAID NIH HHS U01 AI061318NIAID NIH HHS U01 AI070343NIAID NIH HHS U01 AI074518
6 · The paper itself

Abstract

Monoclonal antibodies (mAbs) have long provided powerful research tools for virologists to understand the mechanisms of virus entry into host cells and of antiviral immunity. Even so, commercial development of human (or humanized) mAbs for the prophylaxis, preemptive and acute treatment of viral infections has been slow. This is surprising, as new antibody discovery tools have increased the speed and precision with which potent neutralizing human antiviral mAbs can be identified. As longstanding barriers to antiviral mAb development, such as antigenic variability of circulating viral strains and the ability of viruses to undergo neutralization escape, are being overcome, deeper insight into the mechanisms of mAb action and engineering of effector functions are also improving the efficacy of antiviral mAbs. These successes, in both industrial and academic laboratories, coupled with ongoing changes in the biomedical and regulatory environments, herald an era when the commercial development of human antiviral mAb therapies will likely surge.

Indexed as

Drug DesignForecastingAntibodies, MonoclonalAntiviral AgentsDrug IndustryHumansVirus DiseasesAntibodies, MonoclonalAntiviral Agents

Identifiers

PMID18066039
PMCPMC7097443
OpenAlexW2000984427

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.