scholarly journals Reply to Commentary: “Are HIV-Infected Candidates for Participation in Risky Cure-Related Studies Otherwise Healthy?”

2017 ◽  
Vol 13 (1) ◽  
pp. 23-25 ◽  
Author(s):  
Karine Dubé ◽  
Laurie Sylla ◽  
Lynda Dee

We respond to Eyal et al.’s commentary focusing on how people living with HIV participating in HIV cure-related studies are defined. We argue that the types of participants enrolled in research cannot be dissociated from the study interventions, the types of anticipated risks, and the background standard of care. As the field of HIV cure research advances, more nuance and granularity will be needed to define research criteria and acceptable risk/benefit ratios for cure study participants, as well as specific tiered protocol designs that serve to protect various participant populations from untoward risks, especially in very early phase research with interventions known to have potentially serious toxicities. We highlight key lessons from the ACTIVATE study involving a latency-reversing agent, Panobinostat, for HIV cure study design involving “otherwise healthy volunteers”.

2017 ◽  
Vol 13 (1) ◽  
pp. 3-17 ◽  
Author(s):  
Karine Dubé ◽  
Lynda Dee ◽  
David Evans ◽  
Laurie Sylla ◽  
Jeff Taylor ◽  
...  

Early-phase HIV cure research is conducted against a background of highly effective antiretroviral therapy, and involves risky interventions in individuals who enjoy an almost normal life expectancy. To explore perceptions of three ethical topics in the context of HIV cure research—(a) equipoise, (b) risk–benefit ratios, and (c) “otherwise healthy volunteers”—we conducted 36 in-depth interviews (IDIs) with three groups of purposively selected key informants: clinician-researchers ( n = 11), policy-makers and bioethicists ( n = 13), and people living with HIV (PLWHIV; n = 12). Our analysis revealed variability in perceptions of equipoise. Second, most key informants believed there was no clear measure of risk–benefit ratios in HIV cure research, due in part to the complexity of weighing (sometimes unknown) risks to participants and (sometimes speculative) benefits to science and society. Third, most clinician-researchers and policy-makers/bioethicists viewed potential HIV cure study participants as “otherwise healthy volunteers,” but this perception was not shared among PLWHIV in our study.


2017 ◽  
Vol 3 (1) ◽  
pp. 40-71 ◽  
Author(s):  
Karine Dubé ◽  
David Evans ◽  
Laurie Sylla ◽  
Jeff Taylor ◽  
Bryan J. Weiner ◽  
...  

PLoS ONE ◽  
2020 ◽  
Vol 15 (3) ◽  
pp. e0229733 ◽  
Author(s):  
Jennifer Power ◽  
Gary W. Dowsett ◽  
Andrew Westle ◽  
Joseph D. Tucker ◽  
Sophie Hill ◽  
...  

2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Karine Dubé ◽  
John Kanazawa ◽  
Jeff Taylor ◽  
Lynda Dee ◽  
Nora Jones ◽  
...  

Abstract Background The pursuit of a cure for HIV is a high priority for researchers, funding agencies, governments and people living with HIV (PLWH). To date, over 250 biomedical studies worldwide are or have been related to discovering a safe, effective, and scalable HIV cure, most of which are early translational research and experimental medicine. As HIV cure research increases, it is critical to identify and address the ethical challenges posed by this research. Methods We conducted a scoping review of the growing HIV cure research ethics literature, focusing on articles published in English peer-reviewed journals from 2013 to 2021. We extracted and summarized key developments in the ethics of HIV cure research. Twelve community advocates actively engaged in HIV cure research provided input on this summary and suggested areas warranting further ethical inquiry and foresight via email exchange and video conferencing. Discussion Despite substantial scholarship related to the ethics of HIV cure research, additional attention should focus on emerging issues in six categories of ethical issues: (1) social value (ongoing and emerging biomedical research and scalability considerations); (2) scientific validity (study design issues, such as the use of analytical treatment interruptions and placebos); (3) fair selection of participants (equity and justice considerations); (4) favorable benefit/risk balance (early phase research, benefit-risk balance, risk perception, psychological risks, and pediatric research); (5) informed consent (attention to language, decision-making, informed consent processes and scientific uncertainty); and (6) respect for enrolled participants and community (perspectives of people living with HIV and affected communities and representation). Conclusion HIV cure research ethics has an unfinished agenda. Scientific research and bioethics should work in tandem to advance ethical HIV cure research. Because the science of HIV cure research will continue to rapidly advance, ethical considerations of the major themes we identified will need to be revisited and refined over time.


PLoS ONE ◽  
2018 ◽  
Vol 13 (8) ◽  
pp. e0202647 ◽  
Author(s):  
Jennifer Power ◽  
Andrew Westle ◽  
Gary W. Dowsett ◽  
Jayne Lucke ◽  
Joseph D. Tucker ◽  
...  

2019 ◽  
Vol 46 (3) ◽  
pp. 212-219 ◽  
Author(s):  
Robert Steel

Modern antiretroviral therapies (ART) are capable of suppressing HIV in the bloodstream to undetectable levels. Nonetheless, people living with HIV must maintain lifelong adherence to ART to avoid the re-emergence of the infection. So despite the existence and efficacy of ART, there is still substantial interest in development of a cure. But HIV cure trials can be risky, their success is as of yet unlikely, and the medical gain of being cured is limited against a baseline of ART access. The medical prospect associated with participation in cure research thus look poor. Are the risks and burdens that HIV cure research places on participants so high that it is unethical, at present, to conduct it? In this paper, I answer ‘no’. I start my argument by describing a foundational way of thinking about the ethical justification for regulatory limits on research risk; I then apply this way of thinking to HIV cure trials. In offering this analysis, I confine my attention to studies enrolling competent adults and I also do not consider risks research may pose to third parties or society. Rather, my concern is to engage with the thought that some trials are so risky that performing them is an ethically unacceptable way to treat the participants themselves. I reject this thought and instead argue that there is no level of risk, no matter how high, that inherently mistreats a participant.


2016 ◽  
Vol 2 (3) ◽  
pp. 170-174 ◽  
Author(s):  
Qingyan Ma ◽  
Feng Wu ◽  
Gail Henderson ◽  
Stuart Rennie ◽  
Zachary C. Rich ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document