| Literature DB >> 35413121 |
Julia Li1, Sabine Wellnitz1, Xiaoyuan S Chi1, Yujuan Yue2, Kimberli A Schmidt3, Nancy Nguyen3, Wei Chen1, Irina Yurgelonis1, Eduardo Rojas1, Yuhang Liu3, Jakob Loschko1, Eneida Pollozi1, Yury V Matsuka1, Elie Needle1, Eugene Vidunas1, Robert G K Donald1, Justin Moran1, Kathrin U Jansen1, Philip R Dormitzer1, Peter A Barry2,4,5, Xinzhen Yang1.
Abstract
The development of a vaccine to prevent congenital human cytomegalovirus (HCMV) disease is a public health priority. We tested rhesus CMV (RhCMV) prototypes of HCMV vaccine candidates in a seronegative macaque oral challenge model. Immunogens included a recombinant pentameric complex (PC; gH/gL/pUL128/pUL130/pUL131A), a postfusion gB ectodomain, and a DNA plasmid that encodes pp65-2. Immunization with QS21-adjuvanted PC alone or with the other immunogens elicited neutralizing titers comparable to those elicited by RhCMV infection. Similarly, immunization with all 3 immunogens elicited pp65-specific cytotoxic T-cell responses comparable to those elicited by RhCMV infection. RhCMV readily infected immunized animals and was detected in saliva, blood, and urine after challenge in quantities similar to those in placebo-immunized animals. If HCMV evades vaccine-elicited immunity in humans as RhCMV evaded immunity in macaques, a HCMV vaccine must elicit immunity superior to, or different from, that elicited by the prototype RhCMV vaccine to block horizontal transmission.Entities:
Keywords: RhCMV; cytomegalovirus; neutralizing antibody; protective efficacy; rhesus macaque; vaccine
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Year: 2022 PMID: 35413121 DOI: 10.1093/infdis/jiac129
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 7.759