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1.
Int J Equity Health ; 15(1): 165, 2016 10 04.
Article in English | MEDLINE | ID: mdl-27716301

ABSTRACT

BACKGROUND: Many low- and middle-income countries with a social health insurance system face challenges on their road towards universal health coverage (UHC), especially for people in the informal sector and vulnerable population groups or the informally employed. One way to address this is to subsidize their contributions through general government revenue transfers to the health insurance fund. This paper provides an overview of such health financing arrangements in Asian low- and middle-income countries. The purpose is to assess the institutional design features of government subsidized health insurance type arrangements for vulnerable and informally employed population groups and to explore how these features contribute to UHC progress. METHODS: This regional study is based on a literature search to collect country information on the specific institutional design features of such subsidization arrangements and data related to UHC progress indicators, i.e. population coverage, financial protection and access to care. The institutional design analysis focuses on eligibility rules, targeting and enrolment procedures; financing arrangements; the pooling architecture; and benefit entitlements. RESULTS: Such financing arrangements currently exist in 8 countries with a total of 14 subsidization schemes. The most frequent groups covered are the poor, older persons and children. Membership in these arrangements is mostly mandatory as is full subsidization. An integrated pool for both the subsidized and the contributors exists in half of the countries, which is one of the most decisive features for equitable access and financial protection. Nonetheless, in most schemes, utilization rates of the subsidized are higher compared to the uninsured, but still lower compared to insured formal sector employees. Total population coverage rates, as well as a higher share of the subsidized in the total insured population are related with broader eligibility criteria. CONCLUSIONS: Overall, government subsidized health insurance type arrangements can be effective mechanism to help countries progress towards UHC, yet there is potential to improve on institutional design features as well as implementation.


Subject(s)
Informal Sector , Medical Assistance/organization & administration , Universal Health Insurance/organization & administration , Vulnerable Populations , Asia , Child , Health Services Accessibility , Healthcare Financing , Humans , Medical Assistance/economics , Socioeconomic Factors , Universal Health Insurance/economics
2.
Immunity ; 42(5): 942-52, 2015 May 19.
Article in English | MEDLINE | ID: mdl-25979422

ABSTRACT

CLEC16A variation has been associated with multiple immune-mediated diseases, including type 1 diabetes, multiple sclerosis, systemic lupus erythematosus, celiac disease, Crohn's disease, Addison's disease, primary biliary cirrhosis, rheumatoid arthritis, juvenile idiopathic arthritis, and alopecia areata. Despite strong genetic evidence implicating CLEC16A in autoimmunity, this gene's broad association with disease remains unexplained. We generated Clec16a knock-down (KD) mice in the nonobese diabetic (NOD) model for type 1 diabetes and found that Clec16a silencing protected against autoimmunity. Disease protection was attributable to T cell hyporeactivity, which was secondary to changes in thymic epithelial cell (TEC) stimuli that drive thymocyte selection. Our data indicate that T cell selection and reactivity were impacted by Clec16a variation in thymic epithelium owing to Clec16a's role in TEC autophagy. These findings provide a functional link between human CLEC16A variation and the immune dysregulation that underlies the risk of autoimmunity.


Subject(s)
Autoimmunity/immunology , Epithelial Cells , Lectins, C-Type/metabolism , Monosaccharide Transport Proteins/metabolism , T-Lymphocytes/immunology , Thymus Gland , Animals , Autoimmunity/genetics , Autophagy/immunology , Cell Line , Cells, Cultured , Diabetes Mellitus, Type 1/immunology , Disease Models, Animal , Epithelial Cells/cytology , Epithelial Cells/immunology , Gene Knockdown Techniques , Immunohistochemistry , Lectins, C-Type/genetics , Mice , Mice, Inbred NOD , Monosaccharide Transport Proteins/genetics , Reverse Transcriptase Polymerase Chain Reaction , T-Lymphocytes/cytology , Thymocytes/cytology , Thymocytes/immunology , Thymus Gland/cytology , Thymus Gland/immunology
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