Clarissa Van Hecke

ORCID: 0000-0003-3902-8679
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About
Contact & Profiles
Research Areas
  • HIV Research and Treatment
  • HIV/AIDS drug development and treatment
  • Cancer-related molecular mechanisms research
  • HIV/AIDS Research and Interventions
  • RNA Research and Splicing
  • HIV-related health complications and treatments
  • RNA modifications and cancer
  • CAR-T cell therapy research
  • Hepatitis C virus research
  • RNA Interference and Gene Delivery
  • Hormonal Regulation and Hypertension
  • Electrolyte and hormonal disorders
  • Nanowire Synthesis and Applications
  • interferon and immune responses

Ghent University Hospital
2016-2023

Ghent University
2017-2019

University College London
2017

VIB-UGent Center for Inflammation Research
2017

The Royal Free Hospital
2017

Studying the effects of HIV infection on host transcriptome has typically focused protein-coding genes. However, recent advances in field RNA sequencing revealed that long non-coding RNAs (lncRNAs) add an extensive additional layer to cell's molecular network. Here, we performed profiling throughout a primary vitro investigate lncRNA expression at different replication cycle processes (reverse transcription, integration and particle production). Subsequently, guilt-by-association,...

10.1038/srep36111 article EN cc-by Scientific Reports 2016-10-26

The modification of CD4+ T cells with exogenous nucleic acids or proteins is a critical step in several research and therapeutic applications, such as HIV studies cancer immunotherapies. However, efficient cell transfections are not always easily achieved when working these primary hard-to-transfect cells. While the typically performed by viral transduction electroporation, their use associated safety issues cytotoxicity. Vapor nanobubble (VNB) photoporation sensitizing gold nanoparticles...

10.3390/cryst9080411 article EN cc-by Crystals 2019-08-07

HIV-1 DNA quantification serves as an important reservoir biomarker in HIV cure trials. However, the high genetic diversity of represented by different subtypes may bring inaccuracy quantifying and a sensitive validated assay covering diverse is lacking. Therefore, we cross-validated total assays described literature using three-step comparative analysis. First, bioinformatics tool was developed in-house to perform silico evaluation 67 assays. Secondly, these selected were vitro panel and,...

10.1038/s41598-018-35403-6 article EN cc-by Scientific Reports 2018-11-16

Abstract Background Validated biomarkers to evaluate HIV-1 cure strategies are currently lacking, therefore requiring analytical treatment interruption (ATI) in study participants. Little is known about the safety of ATI and its long-term impact on patient health. Objectives was assessed potential predicting viral rebound were evaluated. Methods PBMCs, plasma CSF collected from 11 HIV-1-positive individuals at four different timepoints during (NCT02641756). Total integrated DNA,...

10.1093/jac/dkaa003 article EN Journal of Antimicrobial Chemotherapy 2020-01-03

BackgroundA wide range of host restriction factors (RF) become upregulated upon HIV-1 infection to suppress viral infectivity and may aid viremic control in vivo. This cross-sectional study evaluated RFs dependency HIV infected individuals with progressive or non-progressive infection, as well early late treated cohorts that exhibit different viro-immunological profiles due differences timing treatment-initiation.MethodsThe expression profile IFIT1, MX1, APOBEC3G, SAMHD1, BST2 (encoding...

10.1016/j.ebiom.2019.02.006 article EN cc-by-nc-nd EBioMedicine 2019-02-12

Lately, the interest in long non-coding RNAs (lncRNAs) as potential drug targets and predictive markers context of HIV-1 has peaked, but their vivo expression regulation remains largely unexplored. Therefore, present study examined lncRNA patterns during a clinical antiretroviral treatment interruption (ATI) trial. Peripheral blood mononuclear cells were isolated from ten patients at four timepoints: prior to ATI, 7-15 days after stop, viral rebound 3 months post therapy re-initiation. RNA...

10.3390/ijms24021031 article EN International Journal of Molecular Sciences 2023-01-05
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