Oliver Laeyendecker

Dr. Oliver Laeyendecker


Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2007 in The Lancet
Verified
Journal Article
Closed access
RGRonald H Gray
Ronald H Gray
GKGodfrey Kigozi
Godfrey Kigozi
DSDavid Serwadda
David Serwadda
FMFrederick Makumbi
Frederick Makumbi
SWStephen Watya
Stephen Watya
MWMaria J Wawer
Maria J Wawer

1 May 2005 in The Journal of Infectious Diseases
Verified
Journal Article
Open access
PDF file
MWMaria J. Wawer
Maria J. Wawer
RGRonald H. Gray
Ronald H. Gray
NSNelson K. Sewankambo
Nelson K. Sewankambo
DSDavid Serwadda
David Serwadda
XLXianbin Li
Xianbin Li
TQThomas C. Quinn
Thomas C. Quinn
BackgroundWe estimated rates of human immunodeficiency virus (HIV)–1 transmission per coital act in HIV-discordant couples by stage of infection in t

26 July 2000 in JAMA
Verified
Journal Article
Open access
PDF file
DTDavid L. Thomas
David L. Thomas
JAJacquie Astemborski
Jacquie Astemborski
RRRudra M. Rai
Rudra M. Rai
FAFrank A. Anania
Frank A. Anania
MSMelody Schaeffer
Melody Schaeffer
DVDavid Vlahov
David Vlahov
There are an estimated 170 million persons worldwide and 3.9 million in the United States who have been infected with hepatitis C virus (HCV).1,2 Hepatitis C virus infection may be self-limited (viral clearance) or persist.3-6 Viral clearance occurs in approximately 15% of persons and is assumed to have occurred when HCV RNA cannot be detected in multiple blood samples from someone with HCV-specific antibodies (anti-HCV) or in whom acute infection was observed.3,4,6,7 In a recent analysis of 43 new HCV infections, we discovered that viral clearance was less common in blacks than whites.4 However, these findings have not been confirmed, and there is little additional information regarding other determinates of viral clearance.

26 March 2009 in New England Journal of Medicine
Verified
Journal Article
Closed access
PDF file
ATAaron A.R. Tobian
Aaron A.R. Tobian
DSDavid Serwadda
David Serwadda
TQThomas C. Quinn
Thomas C. Quinn
GKGodfrey Kigozi
Godfrey Kigozi
PGPatti E. Gravitt
Patti E. Gravitt
RGRonald H. Gray
Ronald H. Gray
Male circumcision significantly reduced the incidence of human immunodeficiency virus (HIV) infection among men in three clinical trials. We assessed the efficacy of male circumcision for the prevention of herpes simplex virus type 2 (HSV-2) and human papillomavirus (HPV) infections and syphilis in HIV-negative adolescent boys and men. We enrolled 5534 HIV-negative, uncircumcised male subjects between the ages of 15 and 49 years in two trials of male circumcision for the prevention of HIV and other sexually transmitted infections. Of these subjects, 3393 (61.3%) were HSV-2–seronegative at enrollment. Of the seronegative subjects, 1684 had been randomly assigned to undergo immediate circumcision (intervention group) and 1709 to undergo circumcision after 24 months (control group). At baseline and at 6, 12, and 24 months, we tested subjects for HSV-2 and HIV infection and syphilis, along with performing physical examinations and conducting interviews. In addition, we evaluated a subgroup of subjects for HPV infection at baseline and at 24 months. At 24 months, the cumulative probability of HSV-2 seroconversion was 7.8% in the intervention group and 10.3% in the control group (adjusted hazard ratio in the intervention group, 0.72; 95% confidence interval [CI], 0.56 to 0.92; P=0.008). The prevalence of high-risk HPV genotypes was 18.0% in the intervention group and 27.9% in the control group (adjusted risk ratio, 0.65; 95% CI, 0.46 to 0.90; P=0.009). However, no significant difference between the two study groups was observed in the incidence of syphilis (adjusted hazard ratio, 1.10; 95% CI, 0.75 to 1.65; P=0.44). In addition to decreasing the incidence of HIV infection, male circumcision significantly reduced the incidence of HSV-2 infection and the prevalence of HPV infection, findings that underscore the potential public health benefits of the procedure. (ClinicalTrials.gov numbers, NCT00425984 and NCT00124878.)

2 November 2020 in Journal of Clinical Investigation
Verified
Journal Article
Closed access
PDF file
SKSabra L. Klein
Sabra L. Klein
Andrew PekoszAndrew Pekosz
Andrew Pekosz
HPHan-Sol Park
Han-Sol Park
RURebecca L. Ursin
Rebecca L. Ursin
JSJanna R. Shapiro
Janna R. Shapiro
ATAaron A.R. Tobian
Aaron A.R. Tobian
Convalescent plasma is a leading treatment for coronavirus disease 2019 (COVID-19), but there is a paucity of data identifying its therapeutic efficacy. Among 126 potential convalescent plasma donors, the humoral immune response was evaluated using a severe acute respiratory syndrome coronavirus 2 (SARS–CoV-2) virus neutralization assay with Vero-E6-TMPRSS2 cells; a commercial IgG and IgA ELISA to detect the spike (S) protein S1 domain (EUROIMMUN); IgA, IgG, and IgM indirect ELISAs to detect the full-length S protein or S receptor–binding domain (S-RBD); and an IgG avidity assay. We used multiple linear regression and predictive models to assess the correlations between antibody responses and demographic and clinical characteristics. IgG titers were greater than either IgM or IgA titers for S1, full-length S, and S-RBD in the overall population. Of the 126 plasma samples, 101 (80%) had detectable neutralizing antibody (nAb) titers. Using nAb titers as the reference, the IgG ELISAs confirmed 95%–98% of the nAb-positive samples, but 20%–32% of the nAb-negative samples were still IgG ELISA positive. Male sex, older age, and hospitalization for COVID-19 were associated with increased antibody responses across the serological assays. There was substantial heterogeneity in the antibody response among potential convalescent plasma donors, but sex, age, and hospitalization emerged as factors that can be used to identify individuals with a high likelihood of having strong antiviral antibody responses.

1 July 2009 in The Lancet
Verified
Journal Article
Closed access
MWMaria J Wawer
Maria J Wawer
FMFrederick Makumbi
Frederick Makumbi
GKGodfrey Kigozi
Godfrey Kigozi
DSDavid Serwadda
David Serwadda
SWStephen Watya
Stephen Watya
RGRonald H Gray
Ronald H Gray