Adjuvant-guided type-1 and type-2 immunity: infectious/noninfectious dichotomy defines the class of response.

Traditionally, protein Ags have been injected in CFA (oil with inactivated mycobacteria) to induce immunity and with IFA (oil alone) to induce tolerance. We report here that injection of hen eggwhite lysozyme, a prototypic Ag, in CFA-induced and IFA-induced pools of hen eggwhite lysozyme-specific memory T cells of comparable fine specificity, clonal size, and avidity spectrum, but with type-1 and type-2 cytokine signatures, respectively. This adjuvant-guided induction of virtually unipolar type-1 and type-2 immunity was observed with seven protein Ags and in a total of six mouse strains. Highly polarized type-1 and type-2 immunity are thus readily achievable through the choice of adjuvant, irrespective of the genetic bias of the host and of the nature of the protein Ag. This finding should have far-reaching implications for the development of vaccines against infectious and autoimmune diseases. Furthermore, our demonstration that Ag injected with IFA is as strongly immunogenic for T cells as it is with CFA shows that the presence of the mycobacteria determines not the priming of naive T cells through the second-signal link but the path of downstream differentiation toward CD4 memory cells that express either type-1 or type-2 cytokines.

Induction of TH1 and TH2 immunity in neonatal mice.

The neonatal period has been thought of as a window in ontogeny, during which the developing immune system is particularly susceptible to tolerization. In the present study, the classic system for induction of neonatal tolerance to protein antigens was reexamined in mice. The presumably tolerogenic protocol was found to trigger a vigorous T helper cell type 2 (TH2) immune response. Thus, neonatal "tolerization" induces immune deviation, not tolerance in the immunological sense. Neonates are not immune privileged but generate TH2 or TH1 responses, depending on the mode of immunization.

Thyroid diagnosis by thermogram sequence analysis.

A computerised thermal imaging system for thyroid diagnosis was developed by the authors and it was discovered that the rate of changes of temperature, rather than the absolute values, associated with a sequence of thermograms could help the medical doctors to identify clinical disorders. In order to further enhance the diagnostic capabilities and speed, a new method for medical thermogram analysis has been developed that compresses a sequence of thermograms into one thermogram while retaining the important information such as the geometrical patterns of the objects and the rate of temperature changes of each pixel within the images. As motion artifacts are unavoidable when a patient undergoes minutes of thermogram recording, direct comparison between images is deemed impossible. A high speed image matching algorithm has been developed to provide an absolute geometrical foundation for pixel-to-pixel comparison. The rate of change of temperature of a particular pixel along the sequence is represented by one single parameter after a process of temperature integration which can then be converted into a corresponding gray level for display. The resultant compressed thermogram can give a clear distinction between problem areas and normal ones. Although our emphasis is on thyroid diagnosis, it is anticipated that this new technique can be applicable to other areas of a human body.