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Herpes simplex virus types 1 and 2 remain clinically important human pathogens, even in the face of one of the most powerful antiviral drugs, acyclovir. In this month's issue, articles from Crute et al. (386) and Kleymann et al. (392) describe two distinct classes of drugs that act on a novel target, the helicase-primase complex of herpes simplex virus. The cover image shows a color-enhanced transmission electron micrograph of herpes simplex virions. Magnification, x40,000.
Is CD4+ cell depletion due to rapid elimination by HIV and failure of the immune system to replace these cells at the required rate? Increasing evidence suggests that this is not the case, and that infection-induced immune activation drives both viral replication and CD4+ cell depletion.
The only targets for clinical treatment of herpes simplex virus infections have been the viral enzymes thymidine kinase and DNA polymerase. Now, animal experiments show the healing benefits of new antiherpes drugs that act on the viral helicase–primase complex and appear superior to the standard treatment, acyclovir.
A study suggesting that many genes, each conferring a small risk, account for most cases of breast cancer could have important implications for population-based prevention programs—provided that the genes can be identified.
Type 1 diabetes has long been thought of as a T cell–mediated disease. Now, a new study in mice makes a strong case that maternal autoantibodies can play an essential role in the initiation of diabetes. (pages 399–402)
Tumor cells engineered to overexpress molecules that activate an immune response have shown therapeutic promise in preventing growth of cancers. In a new study, tumor cells studded with a ligand-mimicking antibody fragment beckon their own destruction. (pages 343–348)
A small-molecular-weight drug originally developed to treat cancer produces sustained reduction in body weight in obese mice by a novel hypothalamic mechanism. The findings suggest new targets for the development of anti-obesity drugs.
The finding that CD39 on Langerhans cells modulates inflammation and immunity in the skin might lead to new strategies to alter immune responses to benefit patients and suggests a new in vitro technique for assessing the irritant potential of topical agents. (pages 358–365)
Proteasome inhibitors have served as critical tools to investigate protein degradation in eukaryotic cells. Now, these inhibitors are proving effective in the treatment of cancer and inflammatory disorders, most recently in animal models of psoriasis.