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  1. Mai CW, Sridhar SB, Karattuthodi MS, Ganesan PM, Shareef J, Lee EL, et al.
    BMJ Open, 2024 Nov 05;14(11):e087064.
    PMID: 39500605 DOI: 10.1136/bmjopen-2024-087064
    INTRODUCTION: Pharmacogenomic testing (PGx) plays a crucial role in improving patient medication safety, yet ethical concerns and limitations impede its clinical implementation in the primary care settings.

    AIMS: To systematically review the current state of PGx in the primary care settings and determine the enablers and challenges of its implementation.

    DESIGN: A scoping review was carried out by adhering to Arksey and O'Malley's 6-stage methodological framework and the 2020 Joanna Briggs Institute and Levac et al. DATA SOURCES: Cochrane Library, EMBASE, Global Health, MEDLINE and PubMed were searched up to 17 July 2023.

    ELIGIBILITY CRITERIA: All peer-reviewed studies in English, reporting the enablers and the challenges of implementing PGx in the primary care settings were included.

    DATE EXTRACTION AND SYNTHESIS: Two independent reviewers extracted the data. Information was synthesised based on the reported enablers and the challenges of implementing PGx testing in the primary care settings. Information was then presented to stakeholders for their inputs.

    RESULTS: 78 studies discussing the implementation of PGx testing are included, of which 57% were published between 2019 and 2023. 68% of the studies discussed PGx testing in the primary care setting as a disease-specific themes. Healthcare professionals were the major stakeholders, with primary care physicians (55%) being the most represented. Enablers encompassed various advantages such as diagnostic and therapeutic benefits, cost reduction and the empowerment of healthcare professionals. Challenges included the absence of sufficient scientific evidence, insufficient training for healthcare professionals, ethical and legal aspects of PGx data, low patient awareness and acceptance and the high costs linked to PGx testing.

    CONCLUSION: PGx testing integration in primary care requires increased consumer awareness, comprehensive healthcare provider training on legal and ethical aspects and global feasibility studies to better understand its implementation challenges. Managing high costs entails streamlining processes, advocating for reimbursement policies and investing in research on innovation and affordability research to improve life expectancy.

  2. Priya S, Malviya R, Chandra P, Sridhar SB, Shareef J, Wadhwa T, et al.
    Parasite Epidemiol Control, 2026 Nov;35:e00557.
    PMID: 42927058 DOI: 10.1016/j.parepi.2026.e00557
    Dengue is a serious mosquito-borne viral disease caused by four antigenically distinct serotypes of the dengue virus, of which DENV-1 and DENV-2 have been found to play significant roles in outbreaks and severe disease across different geographical areas. This review discusses the epidemiology, host-virus interactions, pathogenesis, clinical manifestations, severity, vaccination, and integrated control strategies of DENV-1 and DENV-2. The relevant literature was identified by searching major scientific databases using keywords related to DENV-1, DENV-2, dengue epidemiology, pathogenesis, clinical severity, immune responses, vaccination, and vector control; studies were selected for relevance to the review's objectives. The evidence suggests that DENV-1 and DENV-2 share a number of major mechanisms in causing disease, including viral replication, innate immune modulation, endothelial dysfunction mediated by viral NS1, inflammatory response, and antibody-dependent enhancement, but that clinical outcomes are variable and may depend on viral genotype/lineage, prior dengue exposure, host immunity, age, geographical context, and study population. Furthermore, epidemiological and clinical studies have been unable to rank the severity of DENV-1 and DENV-2, as both serotypes have been reported to cause severe dengue across different settings and conditions. The available data thus suggest that the severity of dengue is multifactorial and not serotype-dependent. Ongoing comparative studies that integrate viral genetics, host immune responses, epidemiology, vaccines, and vector control are needed to enhance serotype-specific dengue prevention and clinical management.
  3. Thakur SK, Malviya R, Chandra P, Sridhar SB, Shareef J, Wadhwa T
    Nanomedicine (Lond), 2026 Nov;21(21):3013-3032.
    PMID: 42965688 DOI: 10.1080/17435889.2026.2754253
    Choroidal melanoma is the most common primary intraocular malignancy, and effective gene therapy remains limited by ocular barriers, tumor heterogeneity, and inefficient nucleic acid delivery. This review critically analyses the molecular rationale, engineering principles, emerging nanoarchitectures, biological validation, and translational prospects of dual-vector nanoengineered mRNA-CRISPR delivery systems for precision gene therapy in choroidal melanoma. The manuscript also highlights key challenges and future strategies for clinical implementation. Current evidence indicates that dual-vector platforms enable independent optimization of mRNA and CRISPR cargos while maintaining coordinated spatiotemporal therapeutic activity. We conducted a literature search in PubMed, Scopus, and Web of Science for relevant studies published from January 2015 to September 2026. Functional cargo partitioning, vector modularity, programmable intracellular trafficking, and ocular-targeted nanoengineering improve delivery precision and reduce biological compromise associated with co-encapsulation. Lipid, polymeric, hybrid, biomimetic, and viral-nonviral architectures each provide distinct engineering advantages depending on therapeutic objectives. Preclinical studies support enhanced genome editing, transient protein restoration, improved tumor suppression, and reduced off-target effects. Nevertheless, manufacturing scalability, regulatory standardization, long-term safety, and clinical validation remain major barriers to translation. Dual-vector nanoengineered mRNA-CRISPR systems represent a promising next-generation platform for precision gene therapy in choroidal melanoma by enabling coordinated and programmable therapeutic delivery. Continued advances in modular nanoengineering, personalized cargo selection, and clinically scalable manufacturing will be essential for successful translation into precision ocular oncology.
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