Vanessa Tenet
Vanessa Tenet has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
John T Schiller
Center for Cancer Research, National Cancer Institute , Bethesda, Maryland
2 shared publicationsKavita Panwar
Virus Reference Department, Public Health Microbiology Division, UK Health Security Agency , London
2 shared publications- Kazutomo Yokoya
Virus Reference Department, Public Health Microbiology Division, UK Health Security Agency , London
2 shared publications - Lisa Mirabello
Division of Cancer Epidemiology and Genetics, National Cancer Institute , Bethesda, Maryland
2 shared publications - Simon Beddows
Virus Reference Department, Public Health Microbiology Division, UK Health Security Agency , London
2 shared publications Filomeno Coelho da Silva
Virus Reference Department, Public Health Microbiology Division, UK Health Security Agency , London
1 shared publication
Latest Publications
- 26 September 2026
- Published by Oxford University Press (OUP) in The Journal of Infectious Diseases
HPV33 and HPV45 Sublineage Antigenicity Defined by Neutralizing Antibodies Elicited During Natural Infection
Human papillomavirus (HPV) variants are classified into lineages and sublineages based upon their genome sequence, but the impact of variation on the function of encoded proteins is unclear. We used a global panel of natural infection sera and relational antigenic maps to assess HPV33 and HPV45 neutralizing antibody specificity. HPV33 A2, A3, B, and C variants were spatially resolved approximately 5-fold distant from the A1 reference, while HPV45 variants were resolved within approximately 2-fold, with differences mapped to residues on the capsid surface. These data inform the degree of lineage and sublineage specificity within the natural infection humoral immune response to oncogenic HPV.
- 26 September 2026
- Published by Oxford University Press (OUP) in The Journal of Infectious Diseases
HPV33 and HPV45 Sublineage Antigenicity Defined by Neutralizing Antibodies Elicited During Natural Infection
Human papillomavirus (HPV) variants are classified into lineages and sublineages based upon their genome sequence, but the impact of variation on the function of encoded proteins is unclear. We used a global panel of natural infection sera and relational antigenic maps to assess HPV33 and HPV45 neutralizing antibody specificity. HPV33 A2, A3, B, and C variants were spatially resolved approximately 5-fold distant from the A1 reference, while HPV45 variants were resolved within approximately 2-fold, with differences mapped to residues on the capsid surface. These data inform the degree of lineage and sublineage specificity within the natural infection humoral immune response to oncogenic HPV.
- Open Access
- 1 October 2025
- Published by Oxford University Press (OUP) in The Journal of Infectious Diseases
- Vol. 233 (1) , e145-e150
Profiling Human Papillomavirus Lineage-Specific Capsid Antigenicity With Geographically Diverse Natural Infection Antibodies
Human papillomavirus variants are classified into lineages based on their whole genome sequence, but the impact of lineage variation on the structure or function of encoded proteins is unclear. We used a global panel of lineage-specific natural infection sera to assess antibody-binding specificity for lineage-specific L1L2 antigens, and we used these data to create relational antigenic maps. Merging these data with neutralizing antibody data demonstrated similar spatial geometry and revealed dependency on a limited number of amino residues on the capsid surface. These data inform the degree of lineage specificity within the natural infection humoral immune response to oncogenic human papillomaviruses.
- 1 October 2025
- Published by Oxford University Press (OUP) in The Journal of Infectious Diseases
- Vol. 233 (1) , e145-e150
Open AccessProfiling Human Papillomavirus Lineage-Specific Capsid Antigenicity With Geographically Diverse Natural Infection Antibodies
Human papillomavirus variants are classified into lineages based on their whole genome sequence, but the impact of lineage variation on the structure or function of encoded proteins is unclear. We used a global panel of lineage-specific natural infection sera to assess antibody-binding specificity for lineage-specific L1L2 antigens, and we used these data to create relational antigenic maps. Merging these data with neutralizing antibody data demonstrated similar spatial geometry and revealed dependency on a limited number of amino residues on the capsid surface. These data inform the degree of lineage specificity within the natural infection humoral immune response to oncogenic human papillomaviruses.