Reformulating severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines with variant strains is being pursued to combat the global surge in infections. We hypothesize that this may be suboptimal due to immune imprinting from earlier vaccination or infection with the original SARS-CoV-2 strain. New strategies may be needed to improve efficacy of SARS-CoV-2 variant vaccines.
The problem of SARS-CoV-2 variants
Neutralizing antibodies correlate with protective immunity for first generation vaccines against SARS-CoV-2 (see Glossary) [1.]. The viral Spike protein is the primary target for neutralizing antibodies and the principal antigen in most vaccines to date. SARS-CoV-2 infection can be prevented in animal models and humans with neutralizing antibodies [2.]. Infection or immunization induce a remarkably robust antibody response in which such immunoglobulins bind a range of epitopes specific to Spike. However, most of these antibodies are nonneutralizing, with only a small fraction of recovered monoclonal antibodies effectively neutralizing SARS-CoV-2 [3.]. Although both nonneutralizing antibodies (including those with Fc-mediated functions) and T cells play an important role in control of many viral infections, including SARS-CoV-2, effective protection from SARS-CoV-2 appears primarily driven by neutralizing antibodies [1.].Several SARS-CoV-2 variants of concern (VOC) harboring mutations in the receptor binding domain (RBD) have emerged that efficiently escape the neutralizing antibody response raised by infection or by currently approved vaccines [4.]. Existing vaccines have lower efficacy in preventing infection with newer or emerging escape variants that suffer neutralization deficits, most notably Beta and Delta variants. Thus, vaccine manufacturers are updating first generation vaccines by replacing the original Spike with the sequence from one or more new variants.This updated vaccine strategy is logical and rapid as it takes advantage of existing vaccine technologies. Early results suggest this may well be at least partially effective, with an updated mRNA booster vaccine (Moderna) expressing Beta Spike eliciting neutralization against this variant in preprimed individuals [5.]. However, boosting with the Beta variant vaccine in the preprimed group resulted in better neutralization of the ancestral SARS-CoV-2 strain than the Beta strain. This suggests that immune imprinting of the response may have occurred. Immune imprinting is a phenomenon whereby initial exposure to one virus strain effectively primes B cell memory and limits the development of memory B cells and neutralizing antibodies against new minor variant strains of the virus [6.]. We hypothesize that repeatedly updating SARS-CoV-2 vaccines might not be fully effective because of limitations imposed by prior immune imprinting to ancestral SARS-CoV-2 strains. Although it is hoped that immune imprinting will not be a major problem for SARS-CoV-2 infections, the possibility that immune imprinting will substantially reduce efficacy of future SARS-CoV-2 vaccines requires action now to both define the extent of the problem and begin to devise solutions.
Immune imprinting in influenza virus infection
Imprinting has been widely studied in influenza A virus (IAV) infections. Each year, seasonal infections with circulating IAVs occur, despite widespread prior infection or vaccination. Accumulated mutations in circulating viruses over time result in escape from neutralizing antibodies (antigenic drift), increasing population level susceptibility [7.]. While overall IAV vaccine effectiveness is around 60%, effectiveness against the A(H3N2) IAV subtype is only around 33% in seasons in which the vaccine and circulating strain are well-matched antigenically and around 23% in seasons when strains are not well matched [7.]. Antigenic drift has been greater among A(H3N2) IAV compared with A(H1N1) IAV and influenza B viruses and, furthermore, vaccination induces substantial ‘back-boosting’ of antibodies against previously circulating A(H3N2) viruses [8.]. IAV vaccines recall memory responses against well-conserved epitopes between the vaccine and past strains but are less effective in generating durable new neutralizing antibodies against variant epitopes of the antigenically drifted viral strain [8.]. Consequently, the immune response becomes ‘imprinted’ against previous strains, limiting robust neutralizing responses to new strains.
Risks of immune imprinting undermining SARS-CoV-2 vaccine efficacy
Similar to antigenically drifted IAV, SARS-CoV-2 neutralization escape variants have only a few key mutations at neutralization epitopes compared with the ancestral strain [4.]. Most antibody responses to Spike are directed against conserved, nonneutralizing epitopes [3.]. Reduced effectiveness is observed against neutralization escape strains relative to ancestral strains for all SARS-CoV-2 vaccines studied to date [9.], suggesting that nonneutralizing responses might only elicit modest protective value against such new strains.A significant difference in immune imprinting between IAV and SARS-CoV-2 is that adult humans have been exposed to IAVs many times during their lifetime. By contrast, SARS-CoV-2 is a new virus and few humans have yet been exposed to more than one SARS-CoV-2 or vaccine strain. It is possible that serial exposure to several related strains might be required to most effectively ‘imprint’ memory B cell immune responses to ancestral SARS-CoV-2 strains and, consequently, limit neutralizing antibody responses to new strains. Nonneutralizing antibodies and T cell responses to conserved epitopes across SARS-CoV-2 will play a role in immunity to new variants [9.], but may be less potently protective than neutralizing antibody responses. As the world grapples with control of SARS-CoV-2 in the coming years, it seems likely that recurrent vaccination or infections will become common and immune imprinting may become an increasingly important issue to consider (Figure 1).
Unknown factors regarding imprinting are the pace at which SARS-CoV-2 variants will emerge, and the magnitude of neutralization escape beyond that currently observed. Optimistically, neutralization escape pathways may be limited and may be already largely exhausted since a few neutralizing epitopes are commonly recognized [10.]. Inducing sufficient neutralizing responses to current escape variants might be achievable with reformulated vaccines. Pessimistically, the SARS-CoV-2 Spike exhibits worrying plasticity, suggesting that further neutralization escape variants may emerge.Evidence for immune imprinting has been suggested by studies of antibody responses against endemic human coronaviruses (hCoV) following SARS-CoV-2 infection [11.] or vaccination [3.]. For instance, back-boosting was observed for antibodies that were crossreactive to both hCoV-HKU1 or hCoV-OC43 and SARS-CoV-2 in samples from subjects recovering from coronavirus disease 2019 (COVID-19), particularly to the conserved S2 region of Spike [11.]. Pre-existing hCoV antibodies were inversely correlated with SARS-CoV-2 de novo antibody responses following COVID-19 [11.]; in particular, the responses were directed against the antigenically distinct SARS-CoV-2 Spike RBD, containing most of the key neutralizing epitopes [3.]. This suggests that pre-existing crossreactive antibodies to Spike can limit new antibody responses to Spike from different viral strains (i.e., hCoVs and SARS-CoV-2); this is consistent with a potential problem of immune imprinting between ancestral and variant strains of SARS-CoV-2.
Strategies to limit immune imprinting from SARS-CoV-2 vaccines
Findings on IAV immune imprinting offer some guidance on strategies to limit the problem of immune imprinting but also suggest caution since, despite extensive research, a universal IAV vaccine remains unavailable. We propose that one strategy may be to immunize individuals only with minimal antigen content needed to induce effective neutralizing antibodies, rather than with the entire protein, which may contain additional ‘distracting’ epitopes that might potentially side-track the immune response [12.]. The stem of the IAV hemagglutinin (HA) protein has been widely studied in this regard. The HA stem is relatively poorly immunogenic on its own, likely due to eliciting low affinity antibodies and weakly inducing T cell help [13.]. However, when the HA stem has been engineered into a full-length HA protein derived from an irrelevant avian IAV strain, vaccination with this chimeric protein has induced robust immune responses in human trials and provided protective immunity in ferret models [14.]. From this rationale, engineering SARS-CoV-2 variant RBDs into heterologous scaffolds such as hCoV Spike proteins might avoid the risk of imprinting with SARS-CoV-2 full-length Spike. Similarly, multimerizing the IAV HA stem and/or presenting it as an ordered array on a nanoparticle can partially overcome the weak immunogenicity of the HA stem [15.]. The SARS-CoV-2 RBD is also relatively weakly immunogenic alone [12.] but multimerization might ameliorate this. Noteworthy, priming with full-length Spike and then boosting with only the SARS-CoV-2 RBD ‘immuno-focuses’ neutralizing antibody responses to the RBD protein
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