{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,12]],"date-time":"2026-03-12T00:59:58Z","timestamp":1773277198398,"version":"3.50.1"},"reference-count":36,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2008,12,8]],"date-time":"2008-12-08T00:00:00Z","timestamp":1228694400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["The Journal of Gene Medicine"],"published-print":{"date-parts":[[2009,2]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>For adenovirus vectors derived from human serotype 5 (Ad5), the efficiency and safety after intravascular delivery is hindered by their sequestration in nontarget tissues, predominantly the liver. The latter is largely dictated by adenovirus binding to blood coagulation zymogens. In addition, several target cells, such as endothelial and smooth muscle cells, are difficult to transduce by Ad5 due to the low expression of the primary coxsackie\u2010adenovirus receptor (CAR). Therefore, alternative adenovirus serotypes are being explored.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>In the present study, we assessed the tropism of mouse adenovirus type 1 (MAV\u20101), a nonhuman adenovirus for which cellular attachment is CAR\u2010independent.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>The typical replication of MAV\u20101 in endothelial cells as observed <jats:italic>in vivo<\/jats:italic> was not reflected in elevated attachment to primary and continuous endothelial cells in cell culture. Remarkably, MAV\u20101 displayed a higher affinity for primary human smooth muscle cells than recombinant Ad5 (rAd5). Attachment of MAV\u20101 to human and mouse cells of hepatocyte origin was not altered by physiological concentrations of human coagulation factor XI (FXI) or the vitamin K\u2010dependent FIX, FX and FVII. By contrast, attachment of Ad5\u2010derived vectors was enhanced at least eight\u2010fold by FX. Using surface plasmon resonance, MAV\u20101 was shown to directly associate with human FX and murine FX and FIX but, opposite to rAd5, this interaction did not lead to enhanced cellular attachment. In intravenously injected severe combined immunodeficiency mice, distribution of MAV\u20101 to the liver was markedly lower than that observed with rAd5.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>Our data on the tropism of MAV\u20101 suggest that this virus may find utility in the field of gene therapy. 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