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1.
Travel Med Infect Dis ; 22: 25-29, 2018.
Article in English | MEDLINE | ID: mdl-29458088

ABSTRACT

The irrational use of antibiotics is increasing in Jordanian refugee camps and consequently so too is bacterial resistance. About one-third of health expenditures at UNRWA health centers in Jordan are attributed to antibiotics. OBJECTIVE: We studied knowledge, attitude and behaviour of Palestine refugees attending UNRWA health centers in Jordan regarding antibiotic use in order to plan public health interventions accordingly. METHODS: A cross-sectional, interviewer-administered survey among 250 adult Palestine refugees at four different health centers was conducted. RESULTS: Irrational antibiotic use was widespread: 63% of patients share antibiotics at home, 38% use left-over antibiotics and 60% purchase antibiotics directly from the pharmacy without prescription (OTC) .1 At the same time, knowledge about antibiotics side effects, resistance, and target agent was low. 90% of patients trust their doctor, however long waiting hours prevent them from seeking medical advice, which significantly increased self-medication. CONCLUSIONS: Our findings suggest a strong need for public education about antibiotics. In addition, health institutional level improvements such as shorter waiting hours and strict regulations prohibiting dispensing without prescription are necessary to combat growing bacterial resistance.


Subject(s)
Anti-Bacterial Agents , Arabs/statistics & numerical data , Drug Resistance, Bacterial , Health Knowledge, Attitudes, Practice , Primary Health Care/statistics & numerical data , Refugees/statistics & numerical data , Adult , Cross-Sectional Studies , Female , Health Services Accessibility/standards , Health Services Accessibility/statistics & numerical data , Humans , Jordan , Male , Risk Factors , Self Medication/statistics & numerical data , United Nations
2.
Nat Commun ; 7: 10875, 2016 Feb 26.
Article in English | MEDLINE | ID: mdl-26915335

ABSTRACT

Autoimmune diseases and other inflammatory conditions are characterized by large lymphocytic tissue infiltrates in which T and B cells can be found in close contact. Here, using a murine airway inflammation model, we compare antigen-specific T and B cells in lung tissue versus lung-draining lymph node. In the lung we identify a B-cell population exhibiting a classical germinal centre phenotype without being organized into ectopic lymphoid tissue. By contrast, classical CXCR5(+) Bcl-6(+) T follicular helper cells are not present. Nevertheless, lung-infiltrating T cells exhibit follicular helper-like properties including the potential to provide help to naive B cells. The lung tissue is also a survival niche for memory T and B cells remaining in residual peribronchial infiltrates after resolution of inflammation. Collectively, this study shows the importance of T/B cooperation not only in lymph nodes but also in inflamed peripheral tissues for local antibody responses to infection and autoimmunity.


Subject(s)
B-Lymphocytes/immunology , Germinal Center/immunology , Lung/immunology , Lymphocyte Cooperation/immunology , Pneumonia/immunology , T-Lymphocyte Subsets/immunology , T-Lymphocytes, Helper-Inducer/immunology , Animals , Antibody Formation/immunology , Autoimmunity/immunology , Coculture Techniques , Disease Models, Animal , Enzyme-Linked Immunosorbent Assay , Flow Cytometry , Inflammation , Lymph Nodes/immunology , Lymphoid Tissue/immunology , Mice , Mice, Transgenic , Ovalbumin/toxicity , Pneumonia/chemically induced , Proto-Oncogene Proteins c-bcl-6 , Receptors, Antigen, T-Cell/genetics , Receptors, CXCR5
3.
J Exp Med ; 212(2): 217-33, 2015 Feb 09.
Article in English | MEDLINE | ID: mdl-25646266

ABSTRACT

The co-stimulators ICOS (inducible T cell co-stimulator) and CD28 are both important for T follicular helper (TFH) cells, yet their individual contributions are unclear. Here, we show that each molecule plays an exclusive role at different stages of TFH cell development. While CD28 regulated early expression of the master transcription factor Bcl-6, ICOS co-stimulation was essential to maintain the phenotype by regulating the novel TFH transcription factor Klf2 via Foxo1. Klf2 directly binds to Cxcr5, Ccr7, Psgl-1, and S1pr1, and low levels of Klf2 were essential to maintain this typical TFH homing receptor pattern. Blocking ICOS resulted in relocation of fully developed TFH cells back to the T cell zone and reversion of their phenotype to non-TFH effector cells, which ultimately resulted in breakdown of the germinal center response. Our study describes for the first time the exclusive role of ICOS and its downstream signaling in the maintenance of TFH cells by controlling their anatomical localization in the B cell follicle.


Subject(s)
Gene Expression Regulation , Inducible T-Cell Co-Stimulator Protein/metabolism , Kruppel-Like Transcription Factors/genetics , Kruppel-Like Transcription Factors/metabolism , Phenotype , T-Lymphocyte Subsets , T-Lymphocytes, Helper-Inducer/immunology , T-Lymphocytes, Helper-Inducer/metabolism , Animals , CD28 Antigens/metabolism , Cell Differentiation/genetics , Cell Differentiation/immunology , Down-Regulation , Female , Forkhead Box Protein O1 , Forkhead Transcription Factors/metabolism , Gene Expression , Germinal Center/immunology , Germinal Center/metabolism , Humans , Inducible T-Cell Co-Stimulator Ligand/metabolism , Membrane Glycoproteins/metabolism , Mice , Mice, Knockout , Palatine Tonsil/immunology , Palatine Tonsil/metabolism , Protein Binding , Receptors, CCR7/metabolism , Receptors, CXCR5/metabolism , Signal Transduction , T-Lymphocytes, Helper-Inducer/cytology
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