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Live Simian Immunodeficiency Virus Vaccine Correlate of Protection: Local Antibody Production and Concentration on the Path of Virus Entry
Author(s) -
Qingsheng Li,
Ming Zeng,
Lijie Duan,
James E. Voss,
Anthony J. Smith,
Stefan E. Pambuccian,
Shangdong Liang,
Stephen W. Wietgrefe,
Peter J. Southern,
Cavan Reilly,
Pamela J. Skinner,
Mary Zupancic,
John V. Carlis,
Michael Piatak,
Diane Waterman,
R. Keith Reeves,
Katherine Masek-Hammerman,
Cynthia A. Derdeyn,
Michael D. Alpert,
David T. Evans,
Heinz Köhler,
Sybille Müller,
James E. Robinson,
Jeffrey D. Lifson,
Dennis R. Burton,
R. Paul Johnson,
Ashley T. Haase
Publication year - 2014
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1400820
Subject(s) - virology , human immunodeficiency virus (hiv) , virus , antibody , simian immunodeficiency virus , biology , simian , immunology
We sought design principles for a vaccine to prevent HIV transmission to women by identifying correlates of protection conferred by a highly effective live attenuated SIV vaccine in the rhesus macaque animal model. We show that SIVmac239Δnef vaccination recruits plasma cells and induces ectopic lymphoid follicle formation beneath the mucosal epithelium in the rhesus macaque female reproductive tract. The plasma cells and ectopic follicles produce IgG Abs reactive with viral envelope glycoprotein gp41 trimers, and these Abs are concentrated on the path of virus entry by the neonatal FcR in cervical reserve epithelium and in vaginal epithelium. This local Ab production and delivery system correlated spatially and temporally with the maturation of local protection against high-dose pathogenic SIV vaginal challenge. Thus, designing vaccines to elicit production and concentration of Abs at mucosal frontlines could aid in the development of an effective vaccine to protect women against HIV-1.

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