This applies specifically to any single study as well as across the entire immune literature. For example, several studies in the elderly have reported reduced lymphocyte proliferation to new antigens,30,31 and others have reported an increased number of CD8+ T cells lacking the co-stimulatory molecule CD28;32–34 but would they be observed in any one individual? The technologies discussed above enable a GSK2656157 mouse high-bandwidth (though not yet comprehensive) enumeration of immune system components and their abundance at the

cell subset, serum protein, gene expression, or Inhibitors,research,lifescience,medical sequence level, providing the first answers to these questions. At present, the high-bandwidth technologies available and discussed here measure distinct components of the immune system: cells types, their communication Inhibitors,research,lifescience,medical with one another, functionality, and specificity. Although these parts are rich in novel information, a more sophisticated level of analysis would integrate multiple components to glean a full view of immunity in man (Figure 3A). The interconnected nature of the immune system would suggest that one layer strongly affects another, yet at this stage it is not clear to what extent measures of one layer would be informative towards another. For instance, to what degree can one estimate serum

protein measures from the abundance Inhibitors,research,lifescience,medical of measured gene expression for gene coding that protein, or learn about cell subset frequencies from measured Inhibitors,research,lifescience,medical gene expression data,20 cell signaling from cell subsets, or cell signaling response from the serum protein which stimulate them? Initial findings from our lab and those of others suggest that the different components of the immune system do indeed reflect what is going on in other parts of the system, but that the reflected information is only partial and a full picture cannot be gleaned without surveying additional

components. Figure 3 A model for one-stop shop human Inhibitors,research,lifescience,medical immune monitoring and a standardized, hospital-driven, immunome project. From these findings, a profiling methodology arises which calls for one-stop shop immune monitoring.35 That is, comprehensive measurement of multiple parts of the immune system from a single sample. Such Adenylyl cyclase profiling, deployed now in an increasing number of “immune monitoring centers” around the world, ourselves included, is yielding massive amounts of data on the immune system of a single individual (Figure 3B).36 Powerful information may be gained through the use of standardized sample assays and shared data repositories that will allow sample comparisons across diseases and experiments. Paralleling the grand scale nature of the Human Genome Project, a call for a large scale “Immunome” project has been made, with the purpose of assaying the diversity of the human immune system in health and disease and establishing proper metrics of immune health.