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1.
Lancet ; 394(10210): 1775-1778, 2019 11 09.
Article in English | MEDLINE | ID: mdl-31676108

ABSTRACT

The Global Kidney Exchange (GKE) programme seeks to facilitate kidney transplants by matching donor-recipient pairs across high-income, medium-income, and low-income countries. The GKE programme pays the medical expenses of people in medium-income and low-income countries, thus enabling them to receive a kidney transplantation they otherwise could not afford. In doing so, the programme increases the global donor pool, and so benefits people in high-income countries by improving their chances of finding a donor match. Nevertheless, the GKE has been accused of being a form of organ trafficking, exploiting the poor, and involving coercion and commodification of donors. We refute these claims, arguing that the GKE promotes global justice and reduces the potential for people in need of kidneys in low-income and medium-income countries to be exploited. Misguided objections should not be allowed to prevent the GKE from realising its potential to reduce suffering and save the lives of rich and poor patients alike.


Subject(s)
Directed Tissue Donation/ethics , Kidney Transplantation/ethics , Humans , Organ Trafficking/ethics , Socioeconomic Factors
3.
5.
Biochem J ; 459(3): 455-66, 2014 May 01.
Article in English | MEDLINE | ID: mdl-24552351

ABSTRACT

Erythroid homoeostasis is primarily controlled by Epo (erythropoietin) receptor signalling; however, the Lyn tyrosine kinase plays an important subsidiary role in regulating the erythroid compartment. Nonetheless, specific erythroid pathways that require Lyn activity and their biological significance remain unclear. To address this, we asked what consequence loss of Lyn had on the ex vivo expansion and maturation of splenic erythroid progenitors and Epo receptor signalling. Pharmacological inhibition of Lyn with PP2 inhibited the survival of terminally differentiated erythroblasts. Less committed erythroid progenitors expanded well, whereas early splenic Lyn(-/-) erythroblasts had attenuated ex vivo expansion, and late stage Lyn(-/-) erythroblasts were retarded in completing morphological maturation ex vivo. Furthermore, immortalized Lyn(-/-) erythroblasts were slower growing, less viable and inhibited in their differentiation. Signalling studies showed that Lyn was required for both positive GAB2/Akt/FoxO3 (forkhead box O3) survival signals as well as negative feedback of JAK2 (Janus kinase 2)/STAT5 (signal transducer and activator of transcription 5) and ERK1/2 (extracellular-signal-regulated kinase 1/2) signals via SHP-1 (Src homology 2 domain-containing protein tyrosine phosphatase 1). During differentiation, Lyn controls survival and cell cycle exit as demonstrated by reduced STAT5 and FoxO3/GSKα/ß (glycogen synthase kinase α/ß) phosphorylation and diminished p27(Kip1) induction in Lyn-deficient erythroblasts. Lyn deficiency alters the balance of pro- and anti-apoptotic molecules (BAD and BclXL), thereby reducing survival and preventing cell cycle exit. Consequently, Lyn facilitates normal erythrocyte production by influencing different stages of erythroid progenitor expansion, and mature cell development and survival signalling.


Subject(s)
Apoptosis Regulatory Proteins/metabolism , Erythroblasts/metabolism , Erythroid Precursor Cells/metabolism , Erythropoiesis , Receptors, Erythropoietin/metabolism , Signal Transduction , src-Family Kinases/metabolism , Animals , Apoptosis Regulatory Proteins/agonists , Apoptosis Regulatory Proteins/antagonists & inhibitors , Cell Differentiation/drug effects , Cell Line, Transformed , Cell Proliferation/drug effects , Cell Survival/drug effects , Cells, Cultured , Embryo, Mammalian/cytology , Erythroblasts/cytology , Erythroblasts/drug effects , Erythroid Precursor Cells/cytology , Erythroid Precursor Cells/drug effects , Erythropoiesis/drug effects , Erythropoietin/pharmacology , Hematinics/pharmacology , Mice , Mice, Inbred C57BL , Mice, Mutant Strains , Protein Kinase Inhibitors/pharmacology , Pyrimidines/pharmacology , Receptors, Erythropoietin/agonists , Signal Transduction/drug effects , Spleen/cytology , src-Family Kinases/antagonists & inhibitors , src-Family Kinases/genetics
6.
Lancet ; 392(10162): 2350, 2018 12 01.
Article in English | MEDLINE | ID: mdl-30527611
7.
Nat Rev Genet ; 9 Suppl 1: S14-9, 2008 10.
Article in English | MEDLINE | ID: mdl-18802416

ABSTRACT

One potential outcome of investing in genomic medicine is the provision of tools for creating a more cost-effective health-care system. Partly with this aim in mind, Thailand has launched two genotyping initiatives: the Thai SNP Discovery Project and the Thai Centre for Excellence in Life Sciences Pharmacogenomics Project. Together, these projects will help Thailand understand the genomic diversity of its population and explore the role that this diversity has in drug response and disease susceptibility in its population. A major future challenge will be for Thailand to integrate genomic medicine in its relatively young universal health-care system.


Subject(s)
Genomics , Universal Health Insurance , Delivery of Health Care/legislation & jurisprudence , Delivery of Health Care/organization & administration , Diffusion of Innovation , Ethnicity , Health Services Accessibility , Humans , Leadership , Politics , Polymorphism, Single Nucleotide , Thailand
8.
Nat Rev Genet ; 9 Suppl 1: S5-9, 2008 10.
Article in English | MEDLINE | ID: mdl-18802419

ABSTRACT

In 2004, the government of Mexico established the National Institute of Genomic Medicine (INMEGEN), to carry out disease-related genomic studies that will address national health problems and stimulate scientific and technological development by generating new commercial products and services in genomic medicine. Towards this end, INMEGEN is carrying out a large-scale genotyping project to map genomic variation within its own population. The initiative is expected to generate a key resource for local researchers to understand disease susceptibility and variation in drug responses, which will contribute to Mexico's goal of developing public health genomics - a field in which Mexico is proving to be a leader amongst emerging economies.


Subject(s)
Academies and Institutes , Developing Countries , Genomics , Public Health , Mexico
9.
Nat Rev Genet ; 9(6): 487-93, 2008 06.
Article in English | MEDLINE | ID: mdl-18487990

ABSTRACT

The notion that developing countries must wait for the developed world to make advances in science and technology that they later import at great cost is being challenged. We have previously argued that developing countries can harness human genetic variation to benefit their populations and economies. Based on our empirical studies of large-scale population genotyping projects in Mexico, India and Thailand, we describe how these resources are being adopted to improve public health and create knowledge-based economies. A significant additional benefit is building the capacity for scientific research and internalizing advances in technology, whatever their source.


Subject(s)
Developing Countries , Genetics, Medical/trends , Genomics/trends , Human Genome Project , Genetic Variation , Genomics/methods , Humans , India , Mexico , Thailand
10.
Nat Rev Genet ; 9 Suppl 1: S19-23, 2008 10.
Article in English | MEDLINE | ID: mdl-18802417

ABSTRACT

The South African government is committed to science and technology innovation, to establishing a knowledge-based economy and to harnessing life-sciences research for health and economic development. Given the constraints and the early stage of development of the field as a whole in South Africa, we found an impressive amount of research on human genomic variation in this country. Encouragingly, South Africa is beginning to apply genomics to address local health needs, including HIV and tuberculosis (TB) infections. We document a number of initiatives in South Africa that are beginning to study genetic variation within the various local indigenous populations. Other early initiatives focus on pharmacogenetic studies, mutation characterization in individual disease genes and genome-wide association studies. Public engagement in genomic issues is spear-headed by The Africa Genome Education Institute.


Subject(s)
Genomics , Biotechnology , Humans , Leadership , Politics , South Africa
11.
Nat Rev Genet ; 9 Suppl 1: S23-7, 2008 10.
Article in English | MEDLINE | ID: mdl-18802418

ABSTRACT

This is a historical moment on the path to genomic medicine - the point at which theory is about to be translated into practice. We have previously described human genome variation studies taking place in Mexico, India, Thailand, and South Africa. Such investments into science and technology will enable these countries to embark on the path to the medical and health applications of genomics, and to benefit economically. Here we provide a perspective on the challenges and opportunities facing these and other countries in the developing world as they begin to harness genomics for the benefit of their populations.


Subject(s)
Delivery of Health Care , Developing Countries , Genomics , Humans , Pharmacogenetics
12.
Nat Rev Genet ; 9 Suppl 1: S9-14, 2008 10.
Article in English | MEDLINE | ID: mdl-18802420

ABSTRACT

India currently has the world's second-largest population along with a fast-growing economy and significant economic disparity. It also continues to experience a high rate of infectious disease and increasingly higher rates of chronic diseases. However, India cannot afford to import expensive technologies and therapeutics nor can it, as an emerging economy, emulate the health-delivery systems of the developed world. Instead, to address these challenges it is looking to biotechnology-based innovation in the field of genomics. The Indian Genome Variation (IGV) consortium, a government-funded collaborative network among seven local institutions, is a reflection of these efforts. The IGV has recently developed the first large-scale database of genomic diversity in the Indian population that will facilitate research on disease predisposition, adverse drug reactions and population migration.


Subject(s)
Genetic Variation , Genome, Human , Awareness , Humans , India/epidemiology , Organizational Innovation , Politics , Private Sector , Public Sector
14.
Nat Genet ; 32(2): 229-32, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12355081

ABSTRACT

Most research into genomics and other related biotechnologies is concerned with the priorities of industrialized nations, and yet a limited number of projects have shown that these technologies could help improve health in developing countries. To encourage the successful application of biotechnology to global health, we carried out a study in which we asked an international group of eminent scientists with expertise in global health issues to identify the top ten biotechnologies for improving health in developing countries. The results offer concrete guidance to those in a position to influence the direction of research and development, and challenge common assumptions about the relevance and affordability of biotechnology for developing countries.


Subject(s)
Biotechnology/trends , Developing Countries , Global Health , Communicable Diseases/diagnosis , Drug Delivery Systems , Forecasting , Vaccines, Synthetic/therapeutic use
15.
Rev Philos Psychol ; 14(1): 113-138, 2023.
Article in English | MEDLINE | ID: mdl-34777639

ABSTRACT

In the first controlled, non-self-report studies to show an influence of university-level ethical instruction on everyday behavior, Schwitzgebel et al. (2020) and Jalil et al. (2020) found that students purchase less meat after exposure to material on the ethics of eating meat. We sought to extend and conceptually replicate this research. Seven hundred thirty students in three large philosophy classes read James Rachels' (2004) "Basic Argument for Vegetarianism", followed by 50-min small-group discussions. Half also viewed a vegetarianism advocacy video containing factory farm footage. A few days after instruction, 54% of students agreed that "eating the meat of factory farmed animals is unethical", compared to 37% before instruction, with no difference between the film and non-film conditions. Also, 39% of students anonymously pledged to avoid eating factory farmed meat for 24 h, again with no statistically detectable difference between conditions. Finally, we obtained 2828 campus food purchase receipts for 113 of the enrolled students who used their Student ID cards for purchases on campus, which we compared with 5033 purchases from a group of 226 students who did not receive the instruction. Meat purchases remained constant in the comparison group and declined among the students exposed to the material, falling from 30% to 23% of purchases overall and from 51% to 42% of purchases of $4.99 or more, with the effect possibly larger in the film condition. Supplementary Information: The online version contains supplementary material available at 10.1007/s13164-021-00583-0.

18.
Health Res Policy Syst ; 10: 18, 2012 Jun 06.
Article in English | MEDLINE | ID: mdl-22672351

ABSTRACT

Biopharmaceutical innovation has had a profound health and economic impact globally. Developed countries have traditionally been the source of most innovations as well as the destination for the resulting economic and health benefits. As a result, most prior research on this sector has focused on developed countries. This paper seeks to fill the gap in research on emerging markets by analyzing factors that influence innovative activity in the indigenous biopharmaceutical sectors of China, India, Brazil, and South Africa. Using qualitative research methodologies, this paper a) shows how biopharmaceutical innovation is taking place within the entrepreneurial sectors of these emerging markets, b) identifies common challenges that indigenous entrepreneurs face, c) highlights the key role played by the state, and d) reveals that the transition to innovation by companies in the emerging markets is characterized by increased global integration. It suggests that biopharmaceutical innovators in emerging markets are capitalizing on opportunities to participate in the drug development value chain and thus developing capabilities and relationships for competing globally both with and against established companies headquartered in developed countries.


Subject(s)
Biopharmaceutics/organization & administration , Developing Countries , Drug Industry/organization & administration , Biopharmaceutics/economics , Biopharmaceutics/legislation & jurisprudence , Biopharmaceutics/trends , Brazil , China , Commerce , Diffusion of Innovation , Drug Industry/economics , Drug Industry/legislation & jurisprudence , Drug Industry/trends , Financing, Organized , Government Programs , Health Workforce/statistics & numerical data , India , Intellectual Property , International Cooperation , Legislation, Drug , Marketing , Research/economics , Research/organization & administration , South Africa , Technology, Pharmaceutical/economics , Technology, Pharmaceutical/legislation & jurisprudence , Technology, Pharmaceutical/organization & administration , Technology, Pharmaceutical/trends
19.
Global Health ; 7: 9, 2011 Apr 20.
Article in English | MEDLINE | ID: mdl-21507259

ABSTRACT

BACKGROUND: Although the World Health Organization had recommended that every child be vaccinated for Hepatitis B by the early 1980s, large multinational pharmaceutical companies held monopolies on the recombinant Hepatitis B vaccine. At a price as high as USD$23 a dose, most Indians families could not afford vaccination. Shantha Biotechnics, a pioneering Indian biotechnology company founded in 1993, saw an unmet need domestically, and developed novel processes for manufacturing Hepatitis B vaccine to reduce prices to less than $1/dose. Further expansion enabled low-cost mass vaccination globally through organizations such as UNICEF. In 2009, Shantha sold over 120 million doses of vaccines. The company was recently acquired by Sanofi-Aventis at a valuation of USD$784 million. METHODS: The case study and grounded research method was used to illustrate how the globalization of healthcare R&D is enabling private sector companies such as Shantha to address access to essential medicines. Sources including interviews, literature analysis, and on-site observations were combined to conduct a robust examination of Shantha's evolution as a major provider of vaccines for global health indications. RESULTS: Shantha's ability to become a significant global vaccine manufacturer and achieve international valuation and market success appears to have been made possible by focusing first on the local health needs of India. How Shantha achieved this balance can be understood in terms of a framework of four guiding principles. First, Shantha identified a therapeutic area (Hepatitis B) in which cost efficiencies could be achieved for reaching the poor. Second, Shantha persistently sought investments and partnerships from non-traditional and international sources including the Foreign Ministry of Oman and Pfizer. Third, Shantha focused on innovation and quality - investing in innovation from the outset yielded the crucial process innovation that allowed Shantha to make an affordable vaccine. Fourth, Shantha constructed its own cGMP facility, which established credibility for vaccine prequalification by the World Health Organization and generated interest from large pharmaceutical companies in its contract research services. These two sources of revenue allowed Shantha to continue to invest in health innovation relevant to the developing world. CONCLUSIONS: The Shantha case study underscores the important role the private sector can play in global health and access to medicines. Home-grown companies in the developing world are becoming a source of low-cost, locally relevant healthcare R&D for therapeutics such as vaccines. Such companies may be compelled by market forces to focus on products relevant to diseases endemic in their country. Sanofi-Aventis' acquisition of Shantha reveals that even large pharmaceutical companies based in the developed world have recognized the importance of meeting the health needs of the developing world. Collectively, these processes suggest an ability to tap into private sector investments for global health innovation, and illustrate the globalization of healthcare R&D to the developing world.

20.
BMC Public Health ; 11: 276, 2011 May 05.
Article in English | MEDLINE | ID: mdl-21545745

ABSTRACT

BACKGROUND: Adequate infant and young child nutrition demands high rates of breastfeeding and good access to nutrient rich complementary foods, requiring public sector action to promote breastfeeding and home based complementary feeding, and private sector action to refrain from undermining breastfeeding and to provide affordable, nutrient rich complementary foods. Unfortunately, due to a lack of trust, the public and private sectors, from both the North and the South, do not work well together in achieving optimal infant and young child nutrition. DISCUSSION: As the current debate in infant and young child nutrition is reminiscent of the "sweatshop" debate fifteen years ago, we argue that lessons from the sweatshops debate regarding cooperation between public and private sectors - and specific organizational experiences such as the Ethical Trading Initiative in which companies, trade unions, and civil society organizations work together to enhance implementation of labour standards and address alleged allegations - could serve as a model for improving cooperation and trust between public, civil society and private groups, and ultimately health, in infant and young child nutrition. SUMMARY: Lessons from the sweatshops debate could serve as a model to promote cooperation and trust between public and private groups, such that they learn to work together towards their common goal of improving infant and young child nutrition.


Subject(s)
Child Nutrition Disorders/prevention & control , Infant Nutrition Disorders/prevention & control , Learning , Public-Private Sector Partnerships , Adolescent , Breast Feeding , Child , Humans , Infant , Infant, Newborn
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