{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T14:48:11Z","timestamp":1786978091175,"version":"build-2736575974"},"reference-count":27,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2005,12,11]],"date-time":"2005-12-11T00:00:00Z","timestamp":1134259200000},"content-version":"vor","delay-in-days":9110,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Medical Virology"],"published-print":{"date-parts":[[1981,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>The 17D vaccine strain of yellow fever virus (17D\u2010YF) produces a safe human arboviral infection that can provide antisera of well\u2010defined specificity under chronologically defined conditions. We studied 17D\u2010YF growth in human peripheral blood macrophages and in two continuous Fc receptor\u2010bearing, macrophage\u2010like cell lines, P388D of mouse origin and U937 of human origin. Cells were infected with virus in the presence or absence of antibody to 17D\u2010YF and to two related flaviviruses, St. Louis encephalitis (SLE) and dengue 2 (D2V). The virus 17D\u2010YF grew in the three cell types when infection was established without antibody; viral yields were increased by addition of antibody to 17D\u2010YF, SLE, and D2V. Increased titers of virus were accompanied by an increased number of infected cells by immunofluorescent assay. Enhancing activity was present in the IgG but not the IgM fractions of immune sera. Infection without cytopathic effect was observed in U937.<\/jats:p>","DOI":"10.1002\/jmv.1890080204","type":"journal-article","created":{"date-parts":[[2007,3,1]],"date-time":"2007-03-01T21:20:36Z","timestamp":1172784036000},"page":"103-117","source":"Crossref","is-referenced-by-count":24,"title":["Antibody\u2010mediated infection of macrophages and macrophage\u2010like cell lines with 17D\u2010yellow fever virus"],"prefix":"10.1002","volume":"8","author":[{"given":"Jacob J.","family":"Schlesinger","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michael W.","family":"Brandriss","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2005,12,11]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"crossref","first-page":"2735","DOI":"10.4049\/jimmunol.125.6.2735","article-title":"Characterization of the Fc receptor for IgG on a human macrophage cell line, U937","volume":"125","author":"Anderson CL","year":"1980","journal-title":"Journal of Immunology"},{"key":"e_1_2_1_3_1","first-page":"2765","article-title":"Genetic approaches to the mechanism of macrophage functions","volume":"37","author":"Bloom BR","year":"1978","journal-title":"Federation Proceedings"},{"issue":"97","key":"e_1_2_1_4_1","first-page":"77","article-title":"Isolation of mononuclear cells and granulocytes from human blood","volume":"21","author":"B\u00f6yum A","year":"1968","journal-title":"Scandanavian Journal of Clinical Laboratory Investigation"},{"key":"e_1_2_1_5_1","first-page":"8.1","volume-title":"Handbook of Experimental Immunology","author":"Fahey JL","year":"1978"},{"key":"e_1_2_1_6_1","doi-asserted-by":"crossref","first-page":"1914","DOI":"10.4049\/jimmunol.123.5.1914","article-title":"Studies on the Fc receptor of the murine macrophage\u2010like cell line P388D1. 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