{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T05:14:53Z","timestamp":1790140493246,"version":"4.0.1"},"reference-count":30,"publisher":"Oxford University Press (OUP)","issue":"11","license":[{"start":{"date-parts":[[2004,12,1]],"date-time":"2004-12-01T00:00:00Z","timestamp":1101859200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2004,12,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>To determine whether inhaled immunostimulatory DNA sequence oligonucleotides containing CpG motifs mitigate the pathophysiologic manifestation of the asthmatic phenotype (airways hyperresponsiveness and airways remodeling), rhesus monkeys with experimentally induced allergic airways disease were treated seven times with inhaled immunostimulatory oligonucleotides (or sham) periodically for 33 weeks. Airways hyperresponsiveness was reduced twofold in immunostimulatory DNA sequence\u2013treated compared with sham-treated monkeys. Airways from immunostimulatory oligonucleotide-treated monkeys had thinner reticular basement membranes, fewer mucous cells, fewer eosinophils, and fewer mast cells than sham-treated allergic monkeys. We conclude that inhaled immunostimulatory oligonucleotides can attenuate the magnitude of airway hyperreactivity and airways remodeling produced in nonhuman primates with experimentally induced allergic airways disease.<\/jats:p>","DOI":"10.1164\/rccm.200404-533oc","type":"journal-article","created":{"date-parts":[[2004,8,11]],"date-time":"2004-08-11T20:24:10Z","timestamp":1092255850000},"page":"1153-1157","source":"Crossref","is-referenced-by-count":60,"title":["Immunostimulatory Oligonucleotides Attenuate Airways Remodeling in Allergic Monkeys"],"prefix":"10.1093","volume":"170","author":[{"given":"Michelle V.","family":"Fanucchi","sequence":"first","affiliation":[{"name":"Center for Comparative Respiratory Biology and Medicine, California National Primate Research Center, University of California, Davis; and School of Medicine, University of California, San Diego, California"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Edward S.","family":"Schelegle","sequence":"additional","affiliation":[{"name":"Center for Comparative Respiratory Biology and Medicine, California National Primate Research Center, University of California, Davis; and School of Medicine, University of California, San Diego, California"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gregory L.","family":"Baker","sequence":"additional","affiliation":[{"name":"Center for Comparative Respiratory Biology and Medicine, California National Primate Research Center, University of California, Davis; and School of Medicine, University of California, San Diego, California"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michael J.","family":"Evans","sequence":"additional","affiliation":[{"name":"Center for Comparative Respiratory Biology and Medicine, California National Primate Research Center, University of California, Davis; and School of Medicine, University of California, San Diego, California"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ruth J.","family":"McDonald","sequence":"additional","affiliation":[{"name":"Center for Comparative Respiratory Biology and Medicine, California National Primate Research Center, University of California, Davis; 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