Journal Article

Nanobodies from camelid mice and llamas neutralize SARS-CoV-2 variants

Hatziioannou, Theodora, Xu, Kai, Nair, Manoj S., Lorenzi, Julio Cesar Cetrulo, Muecksch, Frauke, Tessarollo, Lino, Kwong, Peter D., Teng, I-Ting, Munster, Vincent, Schmidt, Fabian, Wang, Pengfei, Nussenzweig, Michel C., Huang, Yaoxing, Schulz, Jonathan E., Park, Solji, Tsybovsky, Yaroslav, Luo, Yang, Olia, Adam S., Xu, Jianliang, Jung, Seolkyoung, Chuang, Gwo-Yu, Stephens, Tyler, Bylund, Tatsiana, Zhou, Tongqing, Bieniasz, Paul D., Casellas, Rafael, Lieberman, Jenna, Ho, David D., Wang, Zijun, Conte, Andrea

2021

Overview

Since the start of the COVID-19 pandemic, SARS-CoV-2 has caused millions of deaths worldwide. Although a number of vaccines have been deployed, the continual evolution of the receptor-binding domain (RBD) of the virus has challenged their efficacy. In particular, the emerging variants B.1.1.7, B.1.351 and P.1 (first detected in the UK, South Africa and Brazil, respectively) have compromised the efficacy of sera from patients who have recovered from COVID-19 and immunotherapies that have received emergency use authorization 1 – 3 . One potential alternative to avert viral escape is the use of camelid VHHs (variable heavy chain domains of heavy chain antibody (also known as nanobodies)), which can recognize epitopes that are often inaccessible to conventional antibodies 4 . Here, we isolate anti-RBD nanobodies from llamas and from mice that we engineered to produce VHHs cloned from alpacas, dromedaries and Bactrian camels. We identified two groups of highly neutralizing nanobodies. Group 1 circumvents antigenic drift by recognizing an RBD region that is highly conserved in coronaviruses but rarely targeted by human antibodies. Group 2 is almost exclusively focused to the RBD–ACE2 interface and does not neutralize SARS-CoV-2 variants that carry E484K or N501Y substitutions. However, nanobodies in group 2 retain full neutralization activity against these variants when expressed as homotrimers, and—to our knowledge—rival the most potent antibodies against SARS-CoV-2 that have been produced to date. These findings suggest that multivalent nanobodies overcome SARS-CoV-2 mutations through two separate mechanisms: enhanced avidity for the ACE2-binding domain and recognition of conserved epitopes that are largely inaccessible to human antibodies. Therefore, although new SARS-CoV-2 mutants will continue to emerge, nanobodies represent promising tools to prevent COVID-19 mortality when vaccines are compromised. Multivalent nanobodies against SARS-CoV-2 from mice engineered to produce camelid nanobodies recognize conserved epitopes that are inaccessible to human antibodies and show promise as a strategy for dealing with viral escape mutations.

• Publisher: Nature Publishing Group UK,Nature Publishing Group
• Subject: 101/1 / 101/28 / 13/1 / 38/39 / 45/23 / 45/41 / 631/250/2499 / 631/250/255 / 631/326/596/4130 / 82/83 / ACE2 / Angiotensin-converting enzyme 2 / Animals / Antibodies / Antibodies, Neutralizing - chemistry / Antibodies, Neutralizing - genetics / Antibodies, Neutralizing - immunology / Antibodies, Neutralizing - isolation & purification / Antigenic drift / Antigens / Avidity / Binding / Bone marrow / Camelids, New World - genetics / Camelids, New World - immunology / Camels / Chains / Cloning / Coronaviruses / COVID-19 / COVID-19 vaccines / CRISPR-Cas Systems / Disease transmission / Domains / Epitopes / Female / Gene Editing / Genes / HIV / Human immunodeficiency virus / Humanities and Social Sciences / Humans / Immunotherapy / Interferometry / Male / Mice / Mice, Inbred C57BL / Models, Molecular / multidisciplinary / Mutation / Nanobodies / Neutralization / Neutralization Tests / Pandemics / SARS-CoV-2 - chemistry / SARS-CoV-2 - genetics / SARS-CoV-2 - immunology / Science / Science (multidisciplinary) / Severe acute respiratory syndrome coronavirus 2 / Single-Domain Antibodies - chemistry / Single-Domain Antibodies - genetics / Single-Domain Antibodies - immunology / Single-Domain Antibodies - isolation & purification / Somatic Hypermutation, Immunoglobulin - genetics / Spike Glycoprotein, Coronavirus - chemistry / Spike Glycoprotein, Coronavirus - immunology / Stem cells / Vaccines / Viral diseases