1区 · 综合性期刊
Article
作者: Walker, Laura M. ; Champney, Elizabeth ; Graham, Barney S. ; Fels, J. Maximilian ; Burnina, Irina ; McLellan, Jason S. ; Brown, Michael ; Jangra, Rohit K. ; O’Brien, Cecilia M. ; Dye, John M. ; Johnson, Carl ; Burton, Dennis R. ; Lin, Shu ; Wrapp, Daniel ; Florez, Catalina ; Wec, Anna Z. ; Chandran, Kartik ; Johnson, Nicole V. ; Sakharkar, Mrunal ; Sinclair, Melanie ; Dieterle, M. Eugenia ; Laudermilch, Ethan ; Nett, Juergen H. ; Voss, James E. ; Baric, Ralph S. ; Hsieh, Ching-Lin ; Huang, Deli ; Lilov, Asparouh ; Haslwanter, Denise ; Bortz, Robert ; Wang, Nianshuang ; Nemazee, David ; Herbert, Andrew S. ; Maurer, Daniel P. ; Pudi, Sarat ; Wirchnianski, Ariel S. ; Tse, Longping V.
Broadly protective vaccines against known and preemergent human coronaviruses (HCoVs) are urgently needed. To gain a deeper understanding of cross-neutralizing antibody responses, we mined the memory B cell repertoire of a convalescent severe acute respiratory syndrome (SARS) donor and identified 200 SARS coronavirus 2 (SARS-CoV-2) binding antibodies that target multiple conserved sites on the spike (S) protein. A large proportion of the non-neutralizing antibodies display high levels of somatic hypermutation and cross-react with circulating HCoVs, suggesting recall of preexisting memory B cells elicited by prior HCoV infections. Several antibodies potently cross-neutralize SARS-CoV, SARS-CoV-2, and the bat SARS-like virus WIV1 by blocking receptor attachment and inducing S1 shedding. These antibodies represent promising candidates for therapeutic intervention and reveal a target for the rational design of pan-sarbecovirus vaccines.