TY - JOUR
T1 - Synergizing Proteolysis-Targeting Chimeras and Nanoscale Exosome-Based Delivery Mechanisms for HIV and Antiviral Therapeutics
AU - Mukerjee, Nobendu
AU - Maitra, Swastika
AU - Ghosh, Arabinda
AU - Sengupta, Tapti
AU - Alexiou, Athanasios
AU - Subramaniyan, Vetriselvan
AU - Anand, Krishnan
N1 - Funding Information:
The authors would like to acknowledge their respective departments for the conduct of the study.
Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/2/23
Y1 - 2024/2/23
N2 - The global fight against Human Immunodeficiency Virus (HIV) and related viral infections stands at a pivotal juncture, demanding groundbreaking therapeutic strategies. Facing the challenges of existing antiviral treatments, such as viral resistance and nonspecific actions, this paper unveils a transformative approach. We introduce an innovative synergy between proteolysis-targeting chimeras (PROTACs) and exosome-based delivery mechanisms, heralding an innovative era in combating HIV and similar viral diseases. PROTACs emerge as a trailblazing solution, strategically targeting and decomposing crucial viral proteins, and thus, obstructing viral replication and diminishing pathogenesis. Complementing this, the use of exosome-based delivery systems─nature’s own nanoscale couriers─ensures the precise and effective transportation of these dynamic chimeras directly to infected cells and viral reservoirs. This synergistic strategy is not just a leap forward in HIV therapy; it represents a paradigm shift in antiviral interventions at large. The path to realizing the full potential of these avant-garde technologies lies in sustained research investments, cross-disciplinary collaborations, and rigorous safety and efficacy trials. By channeling these efforts toward HIV, a cornerstone in global health research, we are not just envisioning but actively forging path-breaking advancements in antiviral therapeutics. This represents more than scientific progress; it is a beacon of hope, promising to significantly uplift the lives of those battling these formidable diseases.
AB - The global fight against Human Immunodeficiency Virus (HIV) and related viral infections stands at a pivotal juncture, demanding groundbreaking therapeutic strategies. Facing the challenges of existing antiviral treatments, such as viral resistance and nonspecific actions, this paper unveils a transformative approach. We introduce an innovative synergy between proteolysis-targeting chimeras (PROTACs) and exosome-based delivery mechanisms, heralding an innovative era in combating HIV and similar viral diseases. PROTACs emerge as a trailblazing solution, strategically targeting and decomposing crucial viral proteins, and thus, obstructing viral replication and diminishing pathogenesis. Complementing this, the use of exosome-based delivery systems─nature’s own nanoscale couriers─ensures the precise and effective transportation of these dynamic chimeras directly to infected cells and viral reservoirs. This synergistic strategy is not just a leap forward in HIV therapy; it represents a paradigm shift in antiviral interventions at large. The path to realizing the full potential of these avant-garde technologies lies in sustained research investments, cross-disciplinary collaborations, and rigorous safety and efficacy trials. By channeling these efforts toward HIV, a cornerstone in global health research, we are not just envisioning but actively forging path-breaking advancements in antiviral therapeutics. This represents more than scientific progress; it is a beacon of hope, promising to significantly uplift the lives of those battling these formidable diseases.
KW - Exosome-based delivery
KW - HIV
KW - Microbots
KW - PROTACs
KW - TETRACs
UR - http://www.scopus.com/inward/record.url?scp=85185296165&partnerID=8YFLogxK
U2 - 10.1021/acsanm.3c04537
DO - 10.1021/acsanm.3c04537
M3 - Review Article
AN - SCOPUS:85185296165
SN - 2574-0970
VL - 7
SP - 3499
EP - 3514
JO - ACS Applied Nano Materials
JF - ACS Applied Nano Materials
IS - 4
ER -