A click chemistry amplified nanopore assay for ultrasensitive quantification of HIV-1 p24 antigen in clinical samples.
Xiaojun WeiXiaoqin WangZehui ZhangYuanyuan LuoZixin WangWen XiongPiyush K JainJohn R MonnierHui WangTony Y HuChuanbing TangHelmut AlbrechtChang LiuPublished in: Nature communications (2022)
Despite major advances in HIV testing, ultrasensitive detection of early infection remains challenging, especially for the viral capsid protein p24, which is an early virological biomarker of HIV-1 infection. Here, To improve p24 detection in patients missed by immunological tests that dominate the diagnostics market, we show a click chemistry amplified nanopore (CAN) assay for ultrasensitive quantitative detection. This strategy achieves a 20.8 fM (0.5 pg/ml) limit of detection for HIV-1 p24 antigen in human serum, demonstrating 20~100-fold higher analytical sensitivity than nanocluster-based immunoassays and clinically used enzyme-linked immunosorbent assay, respectively. Clinical validation of the CAN assay in a pilot cohort shows p24 quantification at ultra-low concentration range and correlation with CD4 count and viral load. We believe that this strategy can improve the utility of p24 antigen in detecting early infection and monitoring HIV progression and treatment efficacy, and also can be readily modified to detect other infectious diseases.
Keyphrases
- hiv testing
- antiretroviral therapy
- men who have sex with men
- label free
- hiv positive
- hiv infected
- human immunodeficiency virus
- high throughput
- loop mediated isothermal amplification
- gold nanoparticles
- hiv aids
- hepatitis c virus
- real time pcr
- end stage renal disease
- infectious diseases
- quantum dots
- hiv infected patients
- ejection fraction
- peritoneal dialysis
- sars cov
- single molecule
- high resolution
- randomized controlled trial
- newly diagnosed
- south africa
- small molecule
- sensitive detection
- drug discovery
- combination therapy