The rational design of dengue virus (DENV) vaccines requires a detailed understanding of the molecular basis for antibody-mediated immunity. The durably protective antibody response to DENV after primary infection is serotype specific. However, there is an incomplete understanding of the antigenic determinants for DENV type-specific (TS) antibodies, especially for DENV serotype 3, which has only one well-studied, strongly neutralizing human monoclonal antibody (mAb). Here, we investigated the human B cell response in children after natural DENV infection in the endemic area of Nicaragua and isolated 15 DENV3 TS mAbs recognizing the envelope (E) glycoprotein. Functional epitope mapping of these mAbs and small animal prophylaxis studies revealed a complex landscape with protective epitopes clustering in at least 6-7 antigenic sites. Potently neutralizing TS mAbs recognized sites principally in E glycoprotein domains I and II, and patterns suggest frequent recognition of quaternary structures on the surface of viral particles.
Identification of Dengue Virus Serotype 3 Specific Antigenic Sites Targeted by Neutralizing Human Antibodies.
鉴定登革病毒3型特异性抗原位点,该位点可被中和性人类抗体靶向
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作者:Young Ellen, Carnahan Robert H, Andrade Daniela V, Kose Nurgun, Nargi Rachel S, Fritch Ethan J, Munt Jennifer E, Doyle Michael P, White Laura, Baric Thomas J, Stoops Mark, DeSilva Aravinda, Tse Longping V, Martinez David R, Zhu Deanna, Metz Stefan, Wong Marcus P, Espinosa Diego A, Montoya Magelda, Biering Scott B, Sukulpolvi-Petty Soila, Kuan Guillermina, Balmaseda Angel, Diamond Michael S, Harris Eva, Crowe James E Jr, Baric Ralph S
| 期刊: | Cell Host & Microbe | 影响因子: | 18.700 |
| 时间: | 2020 | 起止号: | 2020 May 13; 27(5):710-724 |
| doi: | 10.1016/j.chom.2020.04.007 | 种属: | Human |
| 研究方向: | 免疫/内分泌 | ||
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