Research priorities for an HIV cure: international AIDS society global scientific strategy 2021

SG Deeks, N Archin, P Cannon, S Collins, RB Jones… - Nature medicine, 2021 - nature.com
Despite the success of antiretroviral therapy (ART) for people living with HIV, lifelong
treatment is required and there is no cure. HIV can integrate in the host genome and persist …

Tau: Enabler of diverse brain disorders and target of rapidly evolving therapeutic strategies

CW Chang, E Shao, L Mucke - Science, 2021 - science.org
BACKGROUND The microtubule-associated protein tau has been implicated in the
pathogenesis of Alzheimer's disease and a range of other neurodegenerative disorders …

Droplet digital PCR of viral‎ DNA/RNA, current progress, challenges, and future perspectives

AA Kojabad, M Farzanehpour… - Journal of Medical …, 2021 - Wiley Online Library
High‐throughput droplet‐based digital PCR (ddPCR) is a refinement of the conventional
polymerase chain reaction (PCR)‎ methods. In ddPCR, DNA/RNA is encapsulated …

[HTML][HTML] HIV-1 remission and possible cure in a woman after haplo-cord blood transplant

J Hsu, K Van Besien, MJ Glesby, S Pahwa, A Coletti… - Cell, 2023 - cell.com
Previously, two men were cured of HIV-1 through CCR5Δ32 homozygous (CCR5Δ32/Δ32)
allogeneic adult stem cell transplant. We report the first remission and possible HIV-1 cure in …

HIV-1 and human genetic variation

PJ McLaren, J Fellay - Nature Reviews Genetics, 2021 - nature.com
Over the past four decades, research on the natural history of HIV infection has described
how HIV wreaks havoc on human immunity and causes AIDS. HIV host genomic research …

Targeting CCR5 as a component of an HIV-1 therapeutic strategy

H Mohamed, T Gurrola, R Berman, M Collins… - Frontiers in …, 2022 - frontiersin.org
Globally, human immunodeficiency virus type 1 (HIV-1) infection is a major health burden for
which successful therapeutic options are still being investigated. Challenges facing current …

Gene therapy: a double-edged sword with great powers

R Tang, Z Xu - Molecular and cellular biochemistry, 2020 - Springer
Gene therapy is the treatment of a disease through transferring genetic material into cells of
the patients. In the recent several years, gene therapy has experienced rapid progress and …

CRISPR-Cas9 mediated exonic disruption for HIV-1 elimination

J Herskovitz, M Hasan, M Patel, WR Blomberg… - …, 2021 - thelancet.com
Background A barrier to HIV-1 cure rests in the persistence of proviral DNA in infected CD4+
leukocytes. The high HIV-1 mutation rate leads to viral diversity, immune evasion, and …

[HTML][HTML] Advances in long-acting slow effective release antiretroviral therapies for treatment and prevention of HIV infection

MU Nayan, B Sillman, M Hasan, S Deodhar… - Advanced Drug Delivery …, 2023 - Elsevier
Adherence to daily oral antiretroviral therapy (ART) is a barrier to both treatment and
prevention of human immunodeficiency virus (HIV) infection. To overcome limitations of life …

CCR5 as a coreceptor for human immunodeficiency virus and simian immunodeficiency viruses: a prototypic love-hate affair

AJ Jasinska, I Pandrea, C Apetrei - Frontiers in Immunology, 2022 - frontiersin.org
CCR5, a chemokine receptor central for orchestrating lymphocyte/cell migration to the sites
of inflammation and to the immunosurveillance, is involved in the pathogenesis of a wide …