Abstract

BackgroundThe banking of biological samples raises a number of ethical issues in relation to the storage, export and re-use of samples. Whilst there is a growing body of literature exploring participant perspectives in North America and Europe, hardly any studies have been reported in Africa. This is problematic in particular in light of the growing amount of research taking place in Africa, and with the rise of biobanking practices also on the African continent. In order to investigate the perspectives of African research participants, we conducted a study with research participants in a TB study in the Western Cape, South Africa.MethodsSemi-structured interviews were conducted using an interview guide which drew on the most prominent themes expressed in current literature on sample storage, re-use and exportation. Interviews were conducted in Afrikaans and subsequently translated into English by the same interviewer. Interviews were transcribed verbatim and analysed qualitatively.ResultsThe results of our study indicate that the majority of participants were supportive of giving one-time consent to the storage and re-use of their samples. The concept of research being for a “good cause” was a central prerequisite. Additionally, a significant minority requested that they be re-contacted if a future use was not stipulated on the original consent. There was also considerable variation in how participants understood the concept of a ‘good cause’, with participants describing three distinct categories of research, of which two were generally thought to constitute ‘good cause’ research. Research that was for-profit was considered to fall outside the spectrum of ‘good cause’ research. Participants displayed confidence in the abilities of the researchers to make future decisions regarding sample use, but seemed unaware of the role of ethics committees in either this process or more generally.ConclusionsParticipants expressed a wide and complex range of views about issues of sample storage and re-use, and they showed a great deal of trust in researchers. Participants’ willingness to have their samples stored and re-used is consistent with findings from existing studies. However, in contrast to existing literature, participants were generally not in favour of for-profit research. Further research needs to be done to explore these ideas in other communities, both in South Africa and other countries.

Highlights

  • The banking of biological samples raises a number of ethical issues in relation to the storage, export and re-use of samples

  • Our study aimed to provide a preliminary exploration into these issues, seeking to qualitatively explore the views of research participants on sample storage and re-use

  • In order to explore the views of South African research participants on sample storage and re-use, we set out to conduct a qualitative sociological research study with participants in a current tuberculosis (TB) research project in a high density, low-income urban area in the Western Cape, South Africa

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Summary

Introduction

The banking of biological samples raises a number of ethical issues in relation to the storage, export and re-use of samples. Whilst there is a growing body of literature exploring participant perspectives in North America and Europe, hardly any studies have been reported in Africa. This is problematic in particular in light of the growing amount of research taking place in Africa, and with the rise of biobanking practices on the African continent. Following the sequencing of the human genome, advances in genetics have opened up a plethora of research strategies to investigate disease [1] Pivotal to such strategies is the long-term storage of samples, either as isolated collections or in centralised biobanks, and the re-use of samples and data for multiple projects [2]. Others have argued that broad consent subverts the principle of good informed consent by providing little to no information about ‘future use’ [5]

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