Human papillomavirus 16-specific T cell responses in classic HPV-related vulvar intra-epithelial neoplasia. Determination of strongly immunogenic regions from E6 and E7 proteins

Author:

Bourgault Villada I12,Moyal Barracco M2,Berville S2,Bafounta M L12,Longvert C12,Prémel V1,Villefroy P1,Jullian E13,Clerici T4,Paniel B2,Maillère B5,Choppin J1,Guillet J G1

Affiliation:

1. Institut Cochin, Université Paris Descartes, CNRS (UMR 8104), Département d'Immunologie, Hôpital Cochin, Paris and INSERM, Paris

2. Assistance Publique-Hôpitaux de Paris, Hôpital Ambroise Paré, Service de Dermatologie, Boulogne and Université de Versailles Saint Quentin en Yvelines, Versailles

3. Assistance Publique-Hôpitaux de Paris, Hôpital Saint Vincent de Paul, Service d'Histologie-embryologie cytogénétique – Anatomie pathologique, Paris

4. Assistance Publique-Hôpitaux de Paris, Hôpital Ambroise Paré, Service d'anatomie pathologique, Boulogne

5. CEA-Saclay, Département d'Ingénierie et d'Etudes des Protéines, Gif sur Yvette, France

Abstract

Summary Cell-mediated immunity directed against human papillomavirus 16 (HPV-16) antigens was studied in 16 patients affected with classic vulvar intra-epithelial neoplasia (VIN), also known as bowenoid papulosis (BP). Ten patients had blood lymphocyte proliferative T cell responses directed against E6/2 (14–34) and/or E6/4 (45–68) peptides, which were identified in the present study as immunodominant among HPV-16 E6 and E7 large peptides. Ex vivo enzyme-linked immunospot–interferon (IFN)-γ assay was positive in three patients who had proliferative responses. Twelve months later, proliferative T cell responses remained detectable in only six women and the immunodominant antigens remained the E6/2 (14–34) and E6/4 (45–68) peptides. The latter large fragments of peptides contained many epitopes able to bind to at least seven human leucocyte antigen (HLA) class I molecules and were strong binders to seven HLA-DR class II molecules. In order to build a therapeutic anti-HPV-16 vaccine, E6/2 (14–34) and E6/4 (45–68) fragments thus appear to be good candidates to increase HPV-specific effector T lymphocyte responses and clear classic VIN (BP) disease lesions.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

Reference60 articles.

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