Evidence map›Paper›PMID 40687432›Full record

ReviewInternational journal of microbiology2025

The Confluence of HIV-1 and HIV-2: Implications for Disease Progression and Insights for Therapy.

Edwin Magomere, Charles Ochieng' Olwal, Becky Ewurama Tetteh, Mark Appeaning, Thumbi Ndung'u, George Boateng Kyei, Peter Kojo Quashie

Abstract readReview
In one paragraph

Review in International journal of microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. 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

7 authors.

Edwin MagomereWest African Centre for Cell Biology of Infectious Pathogens, College of Basic and Applied Sciences, University of Ghana, Accra, Ghana.ORCID https://orcid.org/0000-0002-7735-1576
Charles Ochieng' OlwalWest African Centre for Cell Biology of Infectious Pathogens, College of Basic and Applied Sciences, University of Ghana, Accra, Ghana.ORCID https://orcid.org/0000-0003-1747-2963
Becky Ewurama TettehWest African Centre for Cell Biology of Infectious Pathogens, College of Basic and Applied Sciences, University of Ghana, Accra, Ghana.ORCID https://orcid.org/0009-0003-7014-8983
Mark AppeaningWest African Centre for Cell Biology of Infectious Pathogens, College of Basic and Applied Sciences, University of Ghana, Accra, Ghana.ORCID https://orcid.org/0000-0001-5633-4024
Thumbi Ndung'uAfrica Health Research Institute, University of KwaZulu Natal, Durban, South Africa.ORCID https://orcid.org/0000-0003-2962-3992
George Boateng KyeiDepartment of Virology, Noguchi Memorial Institute for Medical Research, University of Ghana, Accra, Ghana.ORCID https://orcid.org/0000-0002-8678-4656
Peter Kojo QuashieWest African Centre for Cell Biology of Infectious Pathogens, College of Basic and Applied Sciences, University of Ghana, Accra, Ghana.ORCID https://orcid.org/0000-0003-4114-5460

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two distinct types of human immunodeficiency virus (HIV), namely, HIV-1 and HIV-2 exist. HIV-1 is responsible for the global pandemic and has an aggressive pathogenesis. On the contrary, HIV-2 is not only less aggressive but also confined to West and Central African regions. Even after four decades of HIV research, a scalable cure or effective vaccine against HIV remains elusive. Consequently, the concept of a functional cure or vaccine, targeting to limit disease progression, allowing sufficient time for the immune response to clear the virus, has gained traction. Efforts to identify new therapeutic targets for development of a functional cure have focused on elite controllers, that is, individuals who naturally control HIV-1 infection in the absence of antiretroviral therapy. However, little progress has been associated with these efforts perhaps due to the scarcity of elite controllers, who make up only 0.15% of HIV-1 infected population globally. A distinct but largely unexplored subset of HIV patients comprise HIV-1 and HIV-2 dually infected individuals. This group of patients naturally presents with an attenuated disease progression phenotype akin to natural controllers. In this review, we discuss the attenuated disease progression phenomenon in dually infected individuals and offer potential explanations for this unanticipated observation. Additionally, we propose potential therapeutic and/or vaccine strategies that could leverage interactions of HIV-1 and HIV-2. Such strategies are likely to inform alternative therapeutics. A thorough understanding of the mechanism underlying the attenuated disease progression phenotype in HIV dually infected individuals is crucial for the design of a functional cure.

Indexed as

attenuated progressioncocirculationdisease progressiondual infectionHIV-1 and HIV-2therapeuticsviral interactions

Identifiers

PMID40687432
PMCPMC12271722

What OpenQuestion holds

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LicenceCC BY
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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.