Structure and Function Analysis of Therapeutic Monoclonal Antibodies against Dengue Virus Type 2

• DOI: 10.1128/jvi.01087-10
• Publication Date: 2010-07-01T02:14:51Z
• Authors: Soila Sukupolvi-P...; S. Kyle Austin; Michael Engle; James D. Brien; Kimberly A. Dowd; Katherine L. Will...; Syd Johnson; Rebeca Rico-Hesse; Eva Harris; Theodore C. Pierson; Daved H. Fremont; Michael S. Diamond
• Keywords: Models, Molecular; 0301 basic medicine; Mice, Inbred BALB C; Binding Sites; Molecular Sequence Data; Antibodies, Monoclonal; Sequence Analysis, DNA; Dengue Virus; Antibodies, Viral; Cell Line; Protein Structure, Tertiary; 3. Good health; Dengue; Mice, Inbred C57BL; Mice; Structure-Activity Relationship; 03 medical and health sciences; Neutralization Tests; Cricetinae; Animals; Humans; Immunotherapy; Epitope Mapping

ABSTRACT

Dengue virus (DENV) is the most prevalent insect-transmitted viral disease in humans globally, and currently no specific therapy or vaccine is available. Protection against DENV and other related flaviviruses is associated with the development of antibodies against the viral envelope (E) protein. Although prior studies have characterized the neutralizing activity of monoclonal antibodies (MAbs) against DENV type 2 (DENV-2), none have compared simultaneously the inhibitory activity against a genetically diverse range of strains in vitro , the protective capacity in animals, and the localization of epitopes. Here, with the goal of identifying MAbs that can serve as postexposure therapy, we investigated in detail the functional activity of a large panel of new anti-DENV-2 mouse MAbs. Binding sites were mapped by yeast surface display and neutralization escape, cell culture inhibition assays were performed with homologous and heterologous strains, and prophylactic and therapeutic activity was evaluated with two mouse models. Protective MAbs localized to epitopes on the lateral ridge of domain I (DI), the dimer interface, lateral ridge, and fusion loop of DII, and the lateral ridge, C-C′ loop, and A strand of DIII. Several MAbs inefficiently inhibited at least one DENV-2 strain of a distinct genotype, suggesting that recognition of neutralizing epitopes varies with strain diversity. Moreover, antibody potency generally correlated with a narrowed genotype and serotype specificity. Five MAbs functioned efficiently as postexposure therapy when administered as a single dose, even 3 days after intracranial infection of BALB/c mice. Overall, these studies define the structural and functional complexity of antibodies against DENV-2 with protective potential.