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Sweat glands are thought of primarily as organs for temperature regulation. Schittek et al. on page 1133 found another valuable function in human sweat: a novel antimicrobial peptide, which they called dermicidin (red). Myoepithelial cells (blue) surround the secretory coil of the eccrine sweat glands (nuclei are green). Dermcidin had antimicro-bial activity at pH and salt concentrations of sweat, making it a candidate for the skin's innate defenses.
A recent workshop was convened under the auspices of the US National Institutes of Health (NIH) to examine the relationship of the innate immune system to autoimmune disorders.
How immature CD4+CD8+ thymocytes become committed to either the CD4 (helper) or CD8 (cytotoxic) lineage is controversial. Genetic ablation of a silencer element in the gene encoding CD4 provides new evidence that CD8 lineage commitment occurs via a stochastic, rather than instructive, mechanism.
Generation of intestinal secretory IgA depends on antigen induction of B cells in organized GALT. A recent paper in Nature reports that in mice the lamina propria provides signals that direct mucosal B cells to undergo Cα class switching and as a basis for SIgA production.
A new family of conserved genes encodes mucin-like glycoproteins. These genes contribute to asthma susceptibility by influencing TH differentiation and cytokine production.
New evidence suggests that mediators of T cell quiescence and immune suppression converge on a common transcriptional program. Tob, a member of a family of anti-proliferation regulators, actively maintains T cell quiescence by interacting with components of the TGF-β signal transduction pathway.
Specialized mouse DCs exist that can recognize the presence of viral pathogens. New evidence shows that these DCs respond by secreting massive amounts of type I IFNs, which may provoke systemic resistance to such pathogens.