TY - JOUR
T1 - Impact of immunization with glycoprotein D2/AS04 on herpes simplex virus type 2 shedding into the genital tract in guinea pigs that become infected
AU - Bourne, Nigel
AU - Milligan, Gregg N.
AU - Stanberry, Lawrence R.
AU - Stegall, Rachael
AU - Pyles, Richard B.
N1 - Funding Information:
Received 19 May 2005; accepted 19 July 2005; electronically published 11 November 2005. Potential conflict of interest: L.R.S. serves as a consultant for GlaxoSmithKline. Financial support: National Institute of Allergy and Infectious Diseases, National Institutes of Health (grant R01 AI052372-01A1). Reprints or correspondence: Dr. Nigel Bourne, Dept. of Pediatrics and Sealy Center for Vaccine Development, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555-0436 ([email protected]).
PY - 2005/12/15
Y1 - 2005/12/15
N2 - In recent clinical trials, a vaccine that contained herpes simplex virus type 2 (HSV-2) glycoprotein D (gD2) and the adjuvant AS04 afforded HSV-seronegative women significant protection against HSV-2 genital disease and limited protection against infection. Similarly, in guinea pigs, immunization with the vaccine provided significant protection against genital HSV-2 disease but did not prevent mucosal infection. We explored the impact of immunization on the magnitude of latent virus infection and on the frequency and magnitude of virus reactivation as measured by both recurrent disease and viral shedding into the genital tract. Guinea pigs immunized with gD2/AS04 were shown by quantitative polymerase chain reaction (qPCR) analysis to have significantly less latent viral DNA in the ganglia than did naive control guinea pigs and to have a reduced incidence and frequency of recurrent disease. By contrast, all immunized guinea pigs shed virus into the genital tract with a frequency comparable to that seen in control guinea pigs. However, the amount of virus shed was significantly reduced, as measured by qPCR. These data suggest that immunization could affect transmission by altering viral shedding patterns.
AB - In recent clinical trials, a vaccine that contained herpes simplex virus type 2 (HSV-2) glycoprotein D (gD2) and the adjuvant AS04 afforded HSV-seronegative women significant protection against HSV-2 genital disease and limited protection against infection. Similarly, in guinea pigs, immunization with the vaccine provided significant protection against genital HSV-2 disease but did not prevent mucosal infection. We explored the impact of immunization on the magnitude of latent virus infection and on the frequency and magnitude of virus reactivation as measured by both recurrent disease and viral shedding into the genital tract. Guinea pigs immunized with gD2/AS04 were shown by quantitative polymerase chain reaction (qPCR) analysis to have significantly less latent viral DNA in the ganglia than did naive control guinea pigs and to have a reduced incidence and frequency of recurrent disease. By contrast, all immunized guinea pigs shed virus into the genital tract with a frequency comparable to that seen in control guinea pigs. However, the amount of virus shed was significantly reduced, as measured by qPCR. These data suggest that immunization could affect transmission by altering viral shedding patterns.
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U2 - 10.1086/498247
DO - 10.1086/498247
M3 - Article
C2 - 16288376
AN - SCOPUS:28844474012
SN - 0022-1899
VL - 192
SP - 2117
EP - 2123
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 12
ER -