Evidence map›Paper›PMID 35911681›Full record

ReviewFrontiers in immunology2022

Challenges and Opportunities of Therapies Targeting Early Life Immunity for Pediatric HIV Cure.

Stella J Berendam, Ashley N Nelson, Bhrugu Yagnik, Ria Goswami, Tiffany M Styles, Margaret A Neja, Caroline T Phan, Sedem Dankwa, Alliyah U Byrd, Carolina Garrido and 4 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

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  13. Accelerated CD8iScience · 2024
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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

14 authors at 5 institutions in 1 country.

Stella J BerendamDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Ashley N NelsonDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Bhrugu YagnikDepartment of Microbiology and Immunology, Emory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA, United States.
Ria GoswamiDepartment of Pediatrics, Weill Cornell Medicine, New York, NY, United States.
Tiffany M StylesDepartment of Microbiology and Immunology, Emory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA, United States.
Margaret A NejaDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, United States.
Caroline T PhanDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Sedem DankwaDepartment of Pediatrics, Weill Cornell Medicine, New York, NY, United States.
Alliyah U ByrdDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Carolina GarridoDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Rama R AmaraDepartment of Microbiology and Immunology, Emory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA, United States.
Ann ChahroudiDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, United States.
Sallie R PermarDepartment of Pediatrics, Weill Cornell Medicine, New York, NY, United States.
Genevieve G FoudaDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
Duke University · USEmory University · USWeill Cornell Medicine · USChildren's Healthcare of Atlanta · USCornell University · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
Pediatric Adolescent Virus Elimination (PAVE) Martin Delaney CollaboratoryUM1AI164566 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Ann M Chahroudi, Deborah Persaud · 2021 to 2026
$35.5M
Ruth L. Kirschstein National Research Service Award (NRSA)- T32T32AI007392 · NIAID · DUKE UNIVERSITY · PI Amy Lynn Corneli, Guido Ferrari · 1990 to 2026
$9.8M
The origin, predictors, and immune correlates of viral rebound in orally SHIV infected infant monkeysP01AI131276 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI FOUDA AMOU OU, GENEVIEVE GINY · 2017 to 2021
$8.3M
Immune interventions in SIV-infected ART-suppressed infant macaquesR01AI133706 · NIAID · EMORY UNIVERSITY · PI CHAHROUDI, ANN M · 2017 to 2021
$4.1M
NIAID NIH HHS P01 AI131276NIAID NIH HHS R01 AI133706NIAID NIH HHS T32 AI007392NIAID NIH HHS UM1 AI164566NIH HHS P51 OD011132
6 · The paper itself

Abstract

Early initiation of antiretroviral therapy (ART) significantly improves clinical outcomes and reduces mortality of infants/children living with HIV. However, the ability of infected cells to establish latent viral reservoirs shortly after infection and to persist during long-term ART remains a major barrier to cure. In addition, while early ART treatment of infants living with HIV can limit the size of the virus reservoir, it can also blunt HIV-specific immune responses and does not mediate clearance of latently infected viral reservoirs. Thus, adjunctive immune-based therapies that are geared towards limiting the establishment of the virus reservoir and/or mediating the clearance of persistent reservoirs are of interest for their potential to achieve viral remission in the setting of pediatric HIV. Because of the differences between the early life and adult immune systems, these interventions may need to be tailored to the pediatric settings. Understanding the attributes and specificities of the early life immune milieu that are likely to impact the virus reservoir is important to guide the development of pediatric-specific immune-based interventions towards viral remission and cure. In this review, we compare the immune profiles of pediatric and adult HIV elite controllers, discuss the characteristics of cellular and anatomic HIV reservoirs in pediatric populations, and highlight the potential values of current cure strategies using immune-based therapies for long-term viral remission in the absence of ART in children living with HIV.

Indexed as

CD4-Positive T-LymphocytesHIV InfectionsAdultChildHumansInfantSecondary Preventioncureearly life immunityHIV cure strategiesimmune-based therapiespediatric HIV

Identifiers

PMID35911681
PMCPMC9325996
OpenAlexW4285084060

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.