Fujisawa Mizuki, Onodera Taishi, Kuroda Daisuke, Kewcharoenwong Chidchamai, Sasaki Michihito, Itakura Yukari, Yumoto Kohei, Nithichanon Arnone, Ito Naoto, Takeoka Shinji, Suzuki Tadaki, Sawa Hirofumi, Lertmemongkolchai Ganjana, Takahashi Yoshimasa
Department of Life Science and Medical Bioscience, Graduate School of Advanced Science and Engineering, Waseda University (TWIns), Tokyo, Japan.
Research Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, Japan.
NPJ Vaccines. 2025 Feb 23;10(1):39. doi: 10.1038/s41541-025-01073-5.
Rabies vaccines require repeated immunization to robustly elicit neutralizing antibodies that prevent fatal diseases. Here, we analyzed rabies glycoprotein antibody repertoires at both polyclonal and monoclonal levels following repeated vaccination. Booster vaccination dramatically elevated the neutralizing activity of recalled antibodies, primarily targeting an immunodominant site III epitope with hydrophilic and rugged structures. Strikingly, the majority of site III-directed antibodies in the recall response used a convergent V gene (IGHV3-30), and they exhibited more hydrophilic and shorter paratopes than non-site III antibodies, providing physicochemical advantages for binding to site III. Additionally, several amino acids on heavy chain CDR3 were identified as key sites for acquiring an ultrapotent neutralizing activity through site III binding. Our in-depth analysis of antibody repertoires revealed the molecular signatures of neutralizing antibodies generated by repeated rabies vaccination, possibly as a result of adaptive convergence.
狂犬病疫苗需要反复免疫才能有力地诱导出中和抗体,从而预防致命疾病。在此,我们分析了反复接种疫苗后多克隆和单克隆水平的狂犬病糖蛋白抗体库。加强免疫显著提高了回忆抗体的中和活性,这些抗体主要靶向具有亲水且粗糙结构的免疫显性III型表位。令人惊讶的是,回忆反应中大多数针对III型表位的抗体使用了趋同的V基因(IGHV3-30),并且它们比非III型表位抗体表现出更多的亲水性和更短的互补决定区,这为与III型表位结合提供了物理化学优势。此外,重链互补决定区3上的几个氨基酸被确定为通过与III型表位结合获得超强中和活性的关键位点。我们对抗体库的深入分析揭示了反复接种狂犬病疫苗产生的中和抗体的分子特征,这可能是适应性趋同的结果。