Euroscicon, The BioPark, Hertfordshire, AL78 3AX, UK
Friday, 12 November 2010
This event has CPD accreditation
9:00 – 9:45 Registration
9:45 – 10:00 Introduction by the Chair: Dr Steven Patterson, Imperial College, London
10:00 – 10:30 Wounding the immune system with its own blade: pathogenic consequences of HIV-mediated pDC activation Dr. Adriano Boasso, Imperial College, Dept. Immunology, Chelsea and Westminster Hospital, UK Human immunodeficiency virus (HIV)-1 infection causes progressive impairment of the immune system in humans, characterized by depletion of CD4 T cells and loss of T cell function. Chronic activation of plasmacytoid dendritic cells (pDC) and subsequent production of type I interferon and indoleamine 2,3-dioxygenase may exert suppressive and cytotoxic effects on T cells. We manipulated HIV in order to reduce its ability to activate pDC and induce immunopathogenesis, while preserving its antigenic potential. More potent T cell memory responses were elicited against non pathogenic HIV, demonstrating that pDC activation may be deleterious rather than beneficial in this setting.
10:30 – 11:00 Talk title to be confirmed Dr Siobhan Burns, Institute of Child Health, UK
11:00- 11:10 Speakers photo
11:10 – 11:30 Mid-morning break and poster viewing
11:30 – 12:00 Talk title to be confirmed Professor Stella Knight, Northwick Park and St. Mark's Campus, Imperial College, London, UK
12:00 – 12:30 Talk title to be confirmed Dr Andrew Stagg, Barts and The London School of Medicine and Dentistry, UK airways.
12:30–13:30 Lunch and Poster Viewing
13:30 - 14: 30 Talk title to be confirmed Diane Razanajaona-Doll, Dendritics SAS, France
14:30 – 15:00 Talk title to be confirmed Professor Giovanna Lombardi - King's College School of Medicine, UK
15:00 – 15:30 Afternoon Tea/Coffee and Last Poster Viewing
15:30 – 16:00 Talk to be confirmed
16:00 – 16:30 Human myeloid dendritic cells, different kinds, different properties Dr Steven Patterson, Imperial College, London A number of distinct types of human myeloid dendritic cells (DC) have been identified. These include monocyte derived DC, Langerhans cells, dermal dendritic cells and blood myeloid (BDCA-1) dendritic cells. Much of our present knowledge of human DC biology has been gained from studies of monocyte derived DC and although this has been a highly valuable model it may not reflect the precise biological properties of different DC populations. Knowledge of the biology of these different DC types is important in the development of vaccines which may target a particular DC population. Aspects of the biology of different types of DC will be presented.
17:00 Chairman’s summing up
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