Abstract: Methods of treating autoimmune diseases, such as vitiligo, by using compositions comprising DNA encoding a variant inducible heat shock protein 70 (HSP70i) having a mutation in the dendritic cell binding region thereof (HSP70i435-447) or an isolated variant gene product in the form of HSP70i with a modification in the dendritic cell activating region thereof (HSP70i435-447).

Abstract: Methods of treating autoimmune diseases, such as vitiligo, by using compositions comprising DNA encoding a variant inducible heat shock protein 70 (HSP70i) having a mutation in the dendritic cell binding region thereof (HSP70i435-447) or an isolated variant gene product in the form of HSP70i with a modification in the dendritic cell activating region thereof (HSP70i435-447).

Abstract: Methods of treating autoimmune diseases, such as vitiligo, by using compositions comprising DNA encoding a variant inducible heat shock protein 70 (HSP70i) having a mutation in the dendritic cell binding region thereof (HSP70i435-447) or an isolated variant gene product in the form of HSP70i with a modification in the dendritic cell activating region thereof (HSP70i435-447).

Abstract: A vaccine and method of treatment suitable for treating autoimmune diseases, such as Vitiligo, by using variant peptides representing a sequence of amino acids found in heat shock protein 70. The vaccine includes a peptide derived from inducible heat shock protein 70 and a plasmid containing a full inducible heat shock protein 70 DNA sequence encoding the peptide.

Abstract: Liposomal system formed from a peptide having a ubiquitinatable region and an antigenic region, a pH-sensitive liposomal carrier; and a bilayer-associated adjuvant, such as MPL are useful as vaccine compositions. These compositions are surprisingly effective in inducing an in vivo immune response to the antigen corresponding to the antigenic region.

Abstract: Therapeutic libraries of minigenes encoding at least one characteristic epitope of a target antigen and degenerate variants of major histocompatability class I restricted epitopes are prepared by constructing a population of minigenes of comparable structure (that is having parallel components at each location in the minigene), each species in the population encoding at least one characteristic epitope of the target antigen and one of a plurality a degenerate variants of an MHC Class I-restricted epitope; screening the population of minigenes in an in vitro or in vivo system to confirm the induction of immunological response against the target antigen; and optionally repeating a screening step on one or more subpopulations of the minigenes to select for immunologically-effective subpopulations, which may comprise as few as a single species of the minigene construct.

Abstract: A tentering machine having a compliant drive link allows for a considerable rate of stretch in a tentered fabric, web or film without the distortion or bowing frequently observed with the tentering machines of the prior art. The tentering machine includes two conveyor tracks adjacent to and facing one another, each conveyor track having a number of fabric edge holders slidingly directable thereabout. A fabric, web or film, grasped on opposite edges by the fabric edge holders, is conveyed thereby through the tentering machine in the space between the two conveyor tracks. Widthwise stretching occurs where the conveyor tracks of the tentering machine have sections on each side of the fabric which diverge from one another, while the two conveyor tracks may be parallel to each other on the two sides of the fabric in applications where prevention of shrinkage is of interest. The fabric edge holders on each conveyor track are run at a substantially common speed by drive chains.