학술논문

Ethical considerations in global HIV phylogenetic research
Document Type
article
Source
The Lancet HIV. 5(11)
Subject
Biomedical and Clinical Sciences
Public Health
Health Sciences
HIV/AIDS
Infectious Diseases
Genetics
8.3 Policy
ethics
and research governance
Health and social care services research
8.1 Organisation and delivery of services
Infection
Good Health and Well Being
Biomedical Research
Guidelines as Topic
HIV
HIV Infections
Human Rights
Humans
Phylogeny
Research Design
Risk Assessment
Ethics in HIV Phylogenetics Working Group
Medical and Health Sciences
Biomedical and clinical sciences
Health sciences
Language
Abstract
Phylogenetic analysis of pathogens is an increasingly powerful way to reduce the spread of epidemics, including HIV. As a result, phylogenetic approaches are becoming embedded in public health and research programmes, as well as outbreak responses, presenting unique ethical, legal, and social issues that are not adequately addressed by existing bioethics literature. We formed a multidisciplinary working group to explore the ethical issues arising from the design of, conduct in, and use of results from HIV phylogenetic studies, and to propose recommendations to minimise the associated risks to both individuals and groups. We identified eight key ethical domains, within which we highlighted factors that make HIV phylogenetic research unique. In this Review, we endeavoured to provide a framework to assist researchers, public health practitioners, and funding institutions to ensure that HIV phylogenetic studies are designed, done, and disseminated in an ethical manner. Our conclusions also have broader relevance for pathogen phylogenetics.