Broadly neutralizing antibodies for HIV-1: efficacies, challenges and opportunities.
Yubin LiuWei CaoMing SunTaisheng LiPublished in: Emerging microbes & infections (2020)
Combination antiretroviral therapy (cART) is effective but not curative, and no successful vaccine is currently available for human immunodeficiency virus-1 (HIV-1). Broadly neutralizing antibodies (bNAbs) provide a new approach to HIV-1 prevention and treatment, and these promising candidates advancing into clinical trials have shown certain efficacies in infected individuals. In addition, bNAbs have the potential to kill HIV-1-infected cells and to affect the course of HIV-1 infection by directly engaging host immunity. Nonetheless, challenges accompany the use of bNAbs, including transient suppression of viraemia, frequent emergence of resistant viruses in rebound viraemia, suboptimal efficacy in virus cell-to-cell transmission, and unclear effects on the cell-associated HIV-1 reservoir. In this review, we discuss opportunities and potential strategies to address current challenges to promote the future use of immunotherapy regimens.
Keyphrases
- antiretroviral therapy
- hiv infected
- human immunodeficiency virus
- hiv positive
- hiv infected patients
- hiv aids
- single cell
- hepatitis c virus
- clinical trial
- cell therapy
- induced apoptosis
- mesenchymal stem cells
- stem cells
- cell cycle arrest
- south africa
- oxidative stress
- dengue virus
- signaling pathway
- rectal cancer
- cell proliferation
- combination therapy