4.8 Article

Cross-Neutralizing and Protective Human Antibody Specificities to Poxvirus Infections

期刊

CELL
卷 167, 期 3, 页码 684-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2016.09.049

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资金

  1. U.S. NIH [U01 AI48512, HHSN272200900047C, U19 AI109948, 8P51 OD 011092-53]
  2. NCRR [UL1 RR024975-01]
  3. National Center for Advancing Translational Sciences [2 UL1 TR000445-06, BX001444]
  4. Vaccine Research Center, National Institute of Allergy and Infectious Diseases, NIH
  5. NIH [P30 CA68485, DK058404]

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Monkeypox (MPXV) and cowpox (CPXV) areemerging agents that cause severe human infections on an inter-mittentbasis, and variola virus (VARV) has potential for use as an agent of bioterror. Vaccinia immune globulin (VIG) has been used therapeutically to treat severe orthopoxvirus infections but is in short supply. We generated a large panel of orthopoxvirus-specific human monoclonal antibodies (Abs) from immune subjects to investigate the molecular basis of broadly neutralizing antibody responses for diverse orthopox-viruses. Detailed analysis revealed the principal neutralizing antibody specificities that are cross-reactive for VACV, CPXV, MPXV, and VARV and that are determinants of protection in murine challenge models. Optimal protection following respiratory or systemic infection required a mixture of Abs that targeted several membrane proteins, including proteins on enveloped and mature virion forms of virus. This work reveals orthopoxvirus targets for human Abs that mediate cross-protective immunity and identifies new candidate Ab therapeutic mixtures to replace VIG.

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