Evidence map›Paper›PMID 16775339›Full record

ArticleJournal of virology2006

Role of maternal autologous neutralizing antibody in selective perinatal transmission of human immunodeficiency virus type 1 escape variants.

Ruth Dickover, Eileen Garratty, Karina Yusim, Catherine Miller, Bette Korber, Yvonne Bryson

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

56 citing papers in PubMed, 99 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

6 authors at 2 institutions in 1 country.

Ruth DickoverDepartment of Pediatrics, David Geffen School of Medicine at UCLA, University of California-Los Angeles, 10833 LeConte Ave., Los Angeles, CA 90095, USA.
Eileen Garratty
Karina Yusim
Catherine Miller
Bette Korber
Yvonne Bryson
Los Alamos National Laboratory · USUniversity of California, Los Angeles · US

Funding

ZDV &3TC NEVIRAPINE COMBINATION THERAPY IN HIV 1 INFECTED INFANTS &M01RR000865 · NCRR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WASHINGTON, ARNOLD E. · 1985 to 2011
$43.4M
CELLULAR IMMUNITY TO HIV IN MOTHERS AND INFANTSR01AI032440 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI UITTENBOGAART, CHRISTEL H. · 1991 to 2000
$402k
METHODS FOR EARLY HIV INFECTION DIAGNOSISR01HD026621 · NICHD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BRYSON, YVONNE J · 1990 to 1992
–
FACTORS INFLUENCING MATERNAL-FETAL HIV TRANSMISSIONR01HD030629 · NICHD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BRYSON, YVONNE J · 1993 to 1997
–
CELLULAR IMMUNE FACTORS IN VERTICAL TRANSMISSION OF HIVR55AI032440 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PLAEGER, SUSAN F. · 1996 to 1996
–
NCRR NIH HHS RR 00865NIAID NIH HHS AI 32440NICHD NIH HHS HD 26621NICHD NIH HHS HD 30629
6 · The paper itself

Abstract

Perinatal human immunodeficiency virus type 1 (HIV-1) transmission is characterized by acquisition of a homogeneous viral quasispecies, yet the selective factors responsible for this genetic bottleneck are unclear. We examined the role of maternal autologous neutralizing antibody (aNAB) in selective transmission of HIV-1 escape variants to infants. Maternal sera from 38 infected mothers at the time of delivery were assayed for autologous neutralizing antibody activity against maternal time-of-delivery HIV-1 isolates in vitro. Maternal sera were also tested for cross-neutralization of infected-infant-first-positive-time-point viral isolates. Heteroduplex and DNA sequence analyses were then performed to identify the initial infecting virus as a neutralization-sensitive or escape HIV-1 variant. In utero transmitters (n = 14) were significantly less likely to have aNAB to their own HIV-1 strains at delivery than nontransmitting mothers (n = 17, 14.3% versus 76.5%, P = 0.003). Cross-neutralization assays of infected-infant-first-positive-time-point HIV-1 isolates indicated that while 14/21 HIV-1-infected infant first positive time point isolates were resistant to their own mother's aNAB, no infant isolate was inherently resistant to antibody neutralization by all sera tested. Furthermore, both heteroduplex (n = 21) and phylogenetic (n = 9) analyses showed that selective perinatal transmission and/or outgrowth of maternal autologous neutralization escape HIV-1 variants occurs in utero and intrapartum. These data indicate that maternal autologous neutralizing antibody can exert powerful protective and selective effects in perinatal HIV-1 transmission and therefore has important implications for vaccine development.

Indexed as

Maternal-Fetal ExchangeAdultAIDS VaccinesAntibodies, ViralBase SequenceFemaleHIV-1HIV SeropositivityHumansInfant, NewbornLabor, ObstetricMolecular Sequence DataNeutralization TestsPhylogenyPregnancyPregnancy Complications, InfectiousAIDS VaccinesAntibodies, Viral

Identifiers

PMID16775339
PMCPMC1488973
OpenAlexW2167983396

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.