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Introduction
The research efforts of the Cellular Immunology Section are focused on the cellular activities of immune cells, pathogenesis and the evaluation of vaccine candidate. The ultimate goal of the section is to conduct researches in the areas of pathogenic materials-immune cell interactions, vaccine trials and immunological monitoring system. The laboratory plans to provide the basis for the evaluation of vaccine candidates for Translational Research Division and Vaccine Development Department, where the goal is to design and develop the immunologic strategies and new vaccines for poor.
 
Basic Aspect
Cellular Immunology Section devotes to (1) the analysis of immunologic mechanisms and principles upon challenges of infection or vaccination, (2) the define novel evaluation technology to pre-exist and new vaccines, (3) analysis of pathogen-immune cell interactions, (4) the discovery of antigenic determinants expressed in target pathogen (along with their function) as vaccine or monoclonal antibody targets, (5) define cellular and/or cell surface markers for (pre)clinical studies to human vaccine trials, (6) cytokine biology as it integrates with infection/immunity/vaccines, (7) collaborative clinical trials involving evaluation of vaccine strategies with a range of animal/human diseases, and (8) the development of new immunoassays to analyze immune responses to vaccines from subjects enrolled in vaccine trials.
 
Ongoing project
One of the main goals in the Cellular Immunology Section is to develop immunologic methods and immunoassays to better define the efficacy of vaccine candidates for a range of human infectious diseases. Further the section is interest in the studying interactions of cytokines on the different arms of the immune system to monitor and optimize the responses to vaccines. It is also important to study the role of the immune responses to human diseases and vaccines and to further define and develop immunodominant determinants and modifications of those determinants toward the optimal activation of human immune responses to target antigens and infection. At the same time we would like to clarify the mechanisms to enhance the potency of antigen-presenting cells in the activation and regulation of the immune response for specific T cell activation and to study the mechanism of the immune response mediated by various immunogens, including conjugate vaccine, vector-based vaccines. Currently we are trying to develop simple cell marker(s) to evaluate cellular activities, which could be used in the clinical trials. This work will be developed in conjunction with Humoral Immunology Section and in parallel with response of immunoglobulins. The laboratory devoted to develop specific types of immunoassays to better evaluate immune responses to target pathogenic antigens as a consequence of vaccination.

The Cellular Immunology Section is trying to provide precise and scientifically sounding mechanism behind vaccination based on currently known and accepted concept such as the role of memory cells. Rapid response to produce neutralizing antibodies and enhancing cytotoxicity are the best example phenomenon upon infection after the vaccination or re-infection. Fundamental question for this is what makes host to respond immediately? It is very likely to have certain cells that recognize specifically invading pathogens not through the ordinary pathway (innate and antigen-presenting process) but educated cells that are able to respond fast, for instance MEMORY CELLS. Staining of phenotypes of these cells has been set in the laboratory and can be monitored in vaccinated subjects. Further activation markers, which is simple to be used, are under investigation for the evaluation of clinical vaccine trial.