In a recent study in Science, Bowen et al.
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report that mutations in Omicron sublineage’s spike protein enhance ACE2 binding,
impair fusogenicity, and dampen the neutralizing activity of antibodies after vaccination
or infection. The data describe how Omicron and especially the BA.5 variant evade
neutralizing antibody responses and argue for using mRNA booster vaccination to increase
immunity.
The SARS-CoV-2 Omicron variant (Pango lineage B.1.1.529) is genetically very different
from the ancestral virus (Wuhan-Hu-1, Pango lineage B). It accounts for almost all
infections during the first six months of 2022. Omicron comprises several sublineages
and BA.5 now replaced the previously dominant sublineages BA.1, BA.2, and BA.2.12.1.
The SARS-CoV-2 spike (S) protein is crucial for cell entry, pathogenicity, and is
the key target of the adaptive immune response. For SARS-CoV-2 attachment, the S protein
binds to the cellular protein angiotensin-converting enzyme 2 (ACE2).
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Subsequently, the S protein is primed by host cell proteases and drives the fusion
of the viral and cellular membranes, which can take place at the plasma membrane or
within endo-/lysosomes. Next, the viral genome is released into the cytoplasm, and
translation of viral proteins and genome replication start. The SARS-CoV-2 S protein
also is a pathogenicity factor. S protein expression on the cell surface leads to
fusion with neighboring cells and the formation of giant cells with multiple nuclei,
so-called syncytia, which were observed in postmortem biopsies from patients that
died from COVID-19. Finally, the SARS-CoV-2 S protein is the main target of neutralizing
antibodies, which are correlated for protection against SARS-CoV-2 infection and severe
COVID-19.
The S proteins of the Omicron sublineages harbor multiple mutations, many of them
reside in the RBD and represent escape mutations that reduce the ability of antibody
binding. While some RBD mutations are known to augment ACE2 binding, most of them
weaken spike-ACE2 interaction. Thus, one would assume that Omicron sublineages would
have reduced ACE2 affinity. However, the opposite is true. Using biolayer interferometry
and surface plasmon resonance analyses, Bowen et al. show that the RBDs of BA.1, BA.2
and BA.4/5 (identical on protein sequence) have a ~2–6-fold higher affinity for ACE2
than the RBDs of the SARS-CoV-2 isolate Wuhan-Hu-1 and the delta variant (Fig. 1a).
Interestingly, the RBD of BA.2.12.1, which differs from the BA.2 RBD by only one mutation,
has a much lower ACE2 affinity than BA.2 RBD, indicating that this difference is due
to mutation L452Q. But why do the RBDs of Omicron sublineages have high affinities
for ACE2 despite harboring several mutations that weaken ACE2 interaction? The answer
is provided by another study, which revealed that some Omicron-specific RBD mutations
establish new ACE2 contacts and thus compensate for RBD mutations that weaken ACE2
interaction.
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Fig. 1
Higher binding affinity, lower syncytium formation, and more immune escape by Omicron.
a The RBDs of BA.1, BA.2 and BA.4/5 have an about 2–6-fold higher affinity for ACE2
than the RBDs of the SARS-CoV-2 isolate Wuhan-Hu-1 and the delta variant. b The S
proteins of all Omicron sublineages are less capable to fuse cells compared to the
S proteins of Wuhan-Hu-1 or Delta, the latter of which is known to possess high cell-cell
fusion capacity. c The polyclonal plasma neutralizing antibody responses (geometric
mean titers, GMT as described in Bowen et al.
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) for Omicron sublineages after homologous prime/boost vaccination showed low titers
and thus significant immune escape when compared to neutralization against ancestral
virus Wuhan-Hu-1 (B.1). The vaccines studied were mRNA-based (Moderna mRNA-1273, Pfizer
BNT162b2), vector-based (Janssen Ad26.COV2.S, AstraZeneca AZD1222, Gamaleya National
Center of Epidemiology and Microbiology Sputnik V), protein-based (Novavax NVX-CoV2373),
and inactivated virions (Sinopharm BBIP-CorV). Triple mRNA-based vaccination resulted
in robust neutralization titers comparable to heterologous mRNA booster, which also
led to appreciable neutralization titers. Plasma antibodies from individuals infected
during the first wave showed little neutralization against Omicron
The SARS-CoV-2 S protein also induces cell-cell fusion when expressed on the cell
surface. Thus, differences in the capability of SARS-CoV-2 variants to cause syncytium
formation may in part reflect their pathogenic potential. Using a cell-cell fusion
assay, Bowen et al. demonstrate that the S proteins of all Omicron sublineages tested
are less capable to fuse cells compared to the S proteins of Wuhan-Hu-1 or Delta,
the latter of which is known to possess high cell-cell fusion capacity (Fig. 1b).
Thus, with respect to causing tissue damage by syncytium formation, Omicron sublineages
appear to have lower pathogenic potential than previous SARS-CoV-2 variants.
Previous work about triple vaccination revealed expansion of pre-existing and de novo
induction of memory B cells specific for the SARS-CoV-2 S protein, leading to antibodies
with enhanced neutralization potency and breadth against variants. In addition, most
monoclonal antibodies showed a substantial drop or even a complete loss of activity
against Omicron sublineages. The work by Bowen and coworkers adds to this by investigating
the plasma neutralizing activity elicited by different vaccine platforms or by vaccinating
inactivated virions. The researchers used pseudotyped vesicular stomatitis virus (VSV)
with S proteins harboring the Omicron mutations to determine immune evasion. They
compared the homologous prime/boost schemes to triple mRNA vaccination or heterologous
booster, when after vector-, protein- or inactivated virion-based homologous vaccinations
mRNA vaccines were used for the third shot. The overall results show a significant
evasion of plasma neutralizing antibody responses against Omicron sublineages when
compared to neutralization against ancestral virus (Fig. 1c). However, triple mRNA-based
vaccination or heterologous mRNA booster resulted in robust neutralization titers
and little immune evasion expressed as fold-change neutralization reduction. The immune
escape especially by BA.4/5 was most prominent after the heterologous booster compared
to triple mRNA vaccination, which may be mechanistically interesting but less relevant
for vaccine efficacy. One should also be cautious when comparing the individual vaccine
regimens, since the cohorts are limited in size, some varying for time intervals between
vaccination and blood withdrawal, and others slightly heterogeneous for vaccine regimens.
There is currently great interest in elucidating differences in the strength and breadth
of the neutralizing antibody response elicited by only infection compared to responses
induced by “hybrid immunity”, namely infection and vaccination. Post-vaccination Omicron
BA.1 breakthrough infection leads to strong neutralizing activity against Omicron
BA.1, BA.2, and earlier SARS-CoV-2 variants of concern, but not against Omicron sublineages
BA.4 and BA.5. It seems that BA.1 breakthrough infections prompted a vigorous recall
response, mostly expanding memory B cells against epitopes shared broadly amongst
variants.
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Preliminary data indicate, however, that a third vaccination six months after the
initial shots did not improve neutralization potency or breadth among convalescent
individuals after COVID-19.
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Thus, the increasing number of vaccinations, vaccine breakthrough or reinfections
will add more complexity to COVID-19 research and for providing advice how to place
adapted mRNA vaccines, which incorporate an Omicron variant strain. For now, the study
by Bowen et al. suggests that despite the fact that Omicron sublineages escape polyclonal
neutralizing antibody responses after a primary vaccine series, vaccine boosters most
likely offer sufficient protection against Omicron-associated severe illness.