Eczema vaccinatum is a potentially fatal, disseminated viral skin infection that develops in individuals with atopic dermatitis after exposure to the vaccinia virus (VV). Despite advances in modern medicine, there are few options for those suffering from disseminated VV infections. Ceragenins (CSAs) are synthetic antimicrobial compounds designed to mimic the structure and function of endogenous antimicrobial peptides (AMPs). We show that CSA-13 exhibits potent antiviral activity against VV by (1) direct antiviral effects against VV; and (2) stimulating the expression of endogenous AMPs with known antiviral activity against VV. In addition, we show that a topical application of CSA-13 penetrates the skin and reduces subsequent satellite lesion formation. This suggests that treatment with CSA-13 may be an intervention for individuals with a disseminated VV skin infection.

Degranulation of basophils and mast cells, releasing histamine, plays a central role in allergic reactions. Degranulation is a response to cell surface receptor aggregation caused by association of receptors with antibodies bound to multivalent antigens. Tools used in studying this process have included small-molecule divalent antigens, but they suffer from weak signaling due to small aggregate size. We have prepared trivalent antigens that allow formation of larger aggregates and potent responses from mast cells.Aggregation of cell surface receptors is a common mechanism involved in signal transduction across cell membranes. 1 This mechanism is used, for example, by receptors that are intrinsic protein tyrosine kinases (i. e., autophosphorylation of aggregated receptors), 2,3 such as the epidermal growth factor receptor, the platelet derived growth factor receptor, and the high affinity receptor for IgE (Fcε RI), which plays a central role in allergic reactions. 4,5 Early steps in the initiation of signaling by this class of receptors are similar: multivalent interactions with a ligand lead to aggregation of receptors and enhanced phosphorylation of tyrosines, which can be recognized by cytoplasmic regulatory molecules.FcεRI receptors are found on the surface of mast cells, basophils, and rat basophilic leukemia (RBL) cells, and these receptors bind the Fc (invariant) region of the divalent antibody IgE. When multiple IgE molecules bind a polyvalent antigen and in turn associate with FcεRI on a cell surface, aggregates of these receptors are generated (Figure 1). Formation of aggregates can in some cases trigger calcium release and degranulation (export of histamine).* paul_savage@byu.edu . Supporting Information Available:Experimental details for the degranulation experiments; a synthetic scheme for 8a and 8b; synthetic details for the preparation of the di-and tri-valent antigens (6a, 6b, 7a, 7b, 8a and 8b); and 1 H NMR spectra for 6a, 6b, 7a, 7b, 8a and 8b. For example, it has been observed that aggregation caused by IgE dimers are less effective than those caused by larger IgE oligomers at stimulating cellular responses 6 and that cellular responses are inhibited when an optimal degree of aggregation is exceeded. 9 The factors that cause an aggregate to be a robust signaling unit, an inhibitor of signal transduction, or a nonsignaling unit remain to be fully elucidated. NIH Public AccessThe importance of influences of ligand-induced receptor aggregates on cellular signals has prompted significant effort in developing means for quantitative analysis of the interactions between multivalent ligands and cell surface receptors. 10 An attractive approach to studing IgE -FcεRI aggregation involves the use of synthetic symmetric divalent ligands, which are the simplest type of ligand capable of aggregating receptors. The interaction of divalent IgE antibodies with a divalent ligand can result in an IgE -FcεRI aggregate spectrum that contains only linear chains and rings of various sizes (including one to on...