Evidence map›Paper›PMID 38386494›Full record

ArticleAIDS research and human retroviruses2024

"This Is Actually a Really Unique Moment in Time": Navigating Long-Acting HIV Treatment and HIV Cure Research with Analytical Treatment Interruptions-A Qualitative Interview Study in the United States.

Karine Dubé, Amaya Perez-Brumer, Hursch Patel, Carina Zhou, Lynda Dee, Gail Graham, Steven Meanley, Morgan Mari Philbin

Open access · greenAbstract read
In one paragraph

Article in AIDS research and human retroviruses, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
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

8 authors at 7 institutions in 2 countries.

Karine DubéDivision of Infectious Diseases and Global Public Health, School of Medicine, University of California San Diego, San Diego, California, USA.ORCID 0000-0003-3458-1539
Amaya Perez-BrumerDalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Hursch PatelDivision of Infectious Diseases and Global Public Health, School of Medicine, University of California San Diego, San Diego, California, USA.
Carina ZhouDivision of Infectious Diseases and Global Public Health, School of Medicine, University of California San Diego, San Diego, California, USA.
Lynda DeeAIDS Action Baltimore, Baltimore, Maryland, USA.
Gail GrahamPATIENTS Program, University of Maryland, College Park, Maryland, USA.
Steven MeanleyDepartment of Family and Community Health, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Morgan Mari PhilbinDivision of Vulnerable Populations, Department of Medicine, University of California San Francisco, San Francisco, California, USA.
University of California System · USAIDS United · USUniversity of California, San Francisco · USUniversity of Maryland, College Park · USUniversity of North Carolina at Chapel Hill · USUniversity of Pennsylvania · USUniversity of Toronto · CA

Funding

BEAT-HIV: Delaney Collaboratory to Cure HIV-1 Infection by Combination ImmunotherapyUM1AI164570 · NIAID · WISTAR INSTITUTE · PI Luis J Montaner, James L. Riley · 2021 to 2026
$34.7M
First-in-human study of two anti-SARS CoV-2 antibodies in health volunteersUM1AI126620 · NIAID · WISTAR INSTITUTE · PI MONTANER, LUIS J, RILEY, JAMES L. · 2016 to 2021
$24.5M
Penn Mental Health AIDS Research CenterP30MH097488 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI Knashawn Hodge Morales · 2013 to 2026
$23.5M
Investigating Psychosocial Experiences of HIV Cure Trial Participants Undergoing Extended HIV Treatment Interruptions: Implications for Ethical ConductR01MH126768 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DUBE, KARINE, SAUCEDA, JOHN ANDREW · 2021 to 2025
$3.6M
Optimizing HIV adherence by developing a shared decision support tool to facilitate women's choice between oral and LAI ARTR34MH124552 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PHILBIN, MORGAN MARI · 2021 to 2023
$773k
Pilot Integration of Participant-Centered Outcomes in HIV Cure Research in the United States: Implications for Ethical ConductR21MH118120 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DUBE, KARINE · 2019 to 2020
$566k
Perceptions of Risks and Benefits of Participating in HIV Cure-related Research among Diverse Youth and Young Adults Living with HIV in the United StatesR21MH122280 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DUBE, KARINE, SABERI, PARYA · 2020 to 2021
$458k
NIAID NIH HHS UM1 AI126620NIAID NIH HHS UM1 AI164570NIMH NIH HHS P30 MH097488NIMH NIH HHS R01 MH126768NIMH NIH HHS R21 MH118120NIMH NIH HHS R21 MH122280NIMH NIH HHS R34 MH124552
6 · The paper itself

Abstract

Advancements in long-acting (LA) HIV treatment and cure research with analytical treatment interruptions (ATIs) have generated important scientific and implementation questions. There is an urgent need to examine challenges navigating the evolving HIV treatment and cure research landscape. From August to October 2022, we conducted 26 semistructured interviews with biomedical researchers and community members representing a predominantly woman demographic to explore the complexity of navigating the rapidly evolving HIV therapeutic and HIV cure research landscape. We purposively sampled individuals recruited from the AIDS Clinical Trials Group and the Martin Delaney Collaboratories for HIV Cure Research. Audio files were transcribed verbatim and analyzed through a thematic approach, using an inductive and iterative process. Among 26 participants, 10 were biomedical researchers and 16 community members, including 11 were people with HIV. Three main themes emerged: (1) We are at a pivotal moment in the evolving landscape of HIV therapeutics and LA HIV treatment and HIV cure research should not be siloed but considered together; (2) There are challenges with engagement in HIV cure research and in switching between oral daily antiretroviral treatment and LA formulations and, mainly, the prolonged pharmacokinetic tail of these compounds matched with limited patient education about their impacts; and (3) There are unique opportunities as a result of this evolving therapeutic landscape, including the key role of decision support for people with HIV, centering around patient autonomy, and the need to learn from the lived experiences of people with HIV who choose LA treatment and/or participation in HIV cure research. Despite a bias toward the woman gender, our study identifies key considerations for navigating concurrent LA HIV treatment and HIV cure research with ATIs from both community members and biomedical researchers' perspectives. Achieving optimal HIV control remains a formidable challenge, necessitating robust interdisciplinary collaborations and engagement with key stakeholders.

Indexed as

Anti-HIV AgentsHIV InfectionsQualitative ResearchAdultBiomedical ResearchFemaleHumansInterviews as TopicMaleMiddle AgedUnited StatesAnti-HIV Agentsanalytical treatment interruptionsantiretroviral treatmentHIVHIV cure researchHIV treatmentlong-acting formulationspharmacokinetic tailsociobehavioral research

Identifiers

PMID38386494
PMCPMC11386995
OpenAlexW4392031950

What OpenQuestion holds

Textmetadata
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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.