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MATE functionality can be categorised under two broad headings: (1) structured data capture, presentation and audit, and (2) advanced evidence-based decision support.
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Other limitations include that the EDDC currently does not capture presentations to all EDs in NSW, so we cannot presently provide a 'whole-of-state' description of ED presentations during the last year of life.
During the study period, the EDDC did not capture presentations to all EDs in NSW, so we were unable to provide a "whole-of-state" description of ED presentations during the last year of life.
The gp120 binding pattern is most similar to that previously reported for inactivated influenza virus (Gonzalez et al., 2010) and although the authors suggest there is little similarity to that pattern, the central conclusion of the influenza study, like the present one, was that SIGN-R1+LN macrophages were involved in antigen capture and presentation to B cells.
Although many of these studies are based on samples from modest numbers of patients, there is value in the systematic capture and presentation of this information alongside large-scale studies such as those presented by TCGA and ICGC.
These tissues are associated with mucosal surfaces of almost any organ, but especially those of the digestive, genitourinary, and respiratory tracts, which are constantly exposed to a wide variety of potentially harmful microorganisms and therefore require their own system of antigen capture and presentation to lymphocytes.
First, BDCA2 is a class II C-type lectin involved in antigen capture and presentation [50], [58].
Although the capture and presentation of invading pathogens is essential for inducing adaptive immune responses, some pathogens escape from full degradation and in fact hijack this system to enhance infection [7], [11].
During pathogenic immune responses like EAE, DCs undergo maturation upon capture and presentation of antigens to T cells in lymphoid organs and in perivascular spaces surrounding the cerebral vessels [25].
The capture and presentation of melanocyte related antigens by different sets of dendritic cells in the skin is an interesting problem that needs to be addressed in future studies.
Because lymphoid organs are settled by successive and different waves of innate cells likely to be involved in antigen capture and presentation to T lymphocytes, we examined whether the accessibility of MVA antigen to different APC subpopulations dictates the occurrence and extent of cellular immunity.
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