Evidence map›Paper›PMID 21655252›Full record

ArticlePloS one2011

Phenotypic characterization of HIV-specific CD8+ T cells during early and chronic infant HIV-1 infection.

Jennifer A Slyker, Grace C John-Stewart, Tao Dong, Barbara Lohman-Payne, Marie Reilly, Ann Atzberger, Stephen Taylor, Elizabeth Maleche-Obimbo, Dorothy Mbori-Ngacha, Sarah L Rowland-Jones

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Endothelial Dysfunction in South African Youth Living With Perinatally Acquired Human Immunodeficiency Virus on Antiretroviral Therapy.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
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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

10 authors at 5 institutions in 4 countries.

Jennifer A SlykerMRC Human Immunology Unit, Oxford University, Oxford, United Kingdom. jslyker@uw.edu
Grace C John-Stewart
Tao Dong
Barbara Lohman-Payne
Marie Reilly
Ann Atzberger
Stephen Taylor
Elizabeth Maleche-Obimbo
Dorothy Mbori-Ngacha
Sarah L Rowland-Jones
University of Oxford · GBMRC Human Immunology Unit · GBUniversity of Nairobi · KEUniversity of Washington · USKarolinska Institutet · SE

Funding

University of Washington/Fred Hutch Center for AIDS ResearchP30AI027757 · NIAID · UNIVERSITY OF WASHINGTON · PI Judith Tsui · 1988 to 2026
$104.9M
VENEREAL DISEASET32AI007140 · NIAID · UNIVERSITY OF WASHINGTON · PI Julia Cook Dombrowski · 1985 to 2026
$19.4M
INTERNATIONAL TRAINING GRANT IN EPIDEMIOLOGYD43TW000007 · FIC · UNIVERSITY OF WASHINGTON · PI FARQUHAR, CAREY · 1988 to 2012
$16.3M
Urgent Versus Post-Stabilization ART in HIV+ Children with Severe Co-infectionsR01HD023412 · NICHD · UNIVERSITY OF WASHINGTON · PI Grace C. John-Stewart, DALTON CHEKOKO WAMALWA · 1987 to 2026
$12.2M
Vertical CMV transmission in the setting of maternal HIV-1 infection in KenyaK01AI087369 · NIAID · UNIVERSITY OF WASHINGTON · PI SLYKER, JENNIFER ANN · 2010 to 2014
$616k
FIC NIH HHS D43 TW000007Medical Research Council G0600520Medical Research Council G0801751Medical Research Council G1001046NIAID NIH HHS K01 AI087369NIAID NIH HHS P30 AI027757NIAID NIH HHS T32 AI007140NICHD NIH HHS R01 HD023412NICHD NIH HHS R01 HD-23412
6 · The paper itself

Abstract

Although CD8(+) T cells play an important role in the containment of adult HIV-1 replication, their role in infant HIV-1 infection is not as well understood. Impaired HIV-specific CD8(+) T cell responses may underlie the persistently high viral loads observed in infants. We examined the frequency and phenotype of infant HIV-specific CD8(+) T cells in 7 HIV-infected antiretroviral therapy-naïve infants during the first 2 years of life, using class I HLA tetramers and IFN-γ-ELISPOT. The frequency (0.088-3.9% of CD3(+)CD8(+) cells) and phenotype (CD27(+)CD28(-), CD45RA(+/-), CD57(+/-), HLA-DR(+), CD95(+)) of infant HIV-specific CD8(+) T cells were similar to reports in adults undergoing early infection. Unlike adults, at 23-24 months post-infection a high frequency of HIV-specific CD8(+) T cells expressed HLA-DR (mean 80%, range 68-85%) and CD95 (mean 88%, range 79-96%), suggesting sustained activation and vulnerability to apoptosis. Despite comparable expansion of HIV-specific CD8(+) T cells of a similar phenotype to adults during early infection, infant T cells failed to contain HIV-1 replication, and remained persistently activated and vulnerable to apoptosis during chronic infection.

Indexed as

CD28 AntigensCD57 AntigensCD8-Positive T-Lymphocytesfas ReceptorHIV-1HIV InfectionsHLA-DR AntigensHumansInfantInfant, NewbornLeukocyte Common AntigensTumor Necrosis Factor Receptor Superfamily, Member 7CD28 AntigensCD57 Antigensfas ReceptorHLA-DR AntigensLeukocyte Common AntigensTumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID21655252
PMCPMC3105047
OpenAlexW2079325774

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.