The development of an effective AIDS vaccine remains a challenge. Nucleoside-modified mRNAs formulated in lipid nanoparticles (mRNA-LNP) have proved to be a potent mode of immunization against infectious diseases in preclinical studies, and are being tested for SARS-CoV-2 in humans. A critical question is how mRNA-LNP vaccine immunogenicity compares to that of traditional adjuvanted protein vaccines in primates. Here, we show that mRNA-LNP immunization compared to protein immunization elicits either the same or superior magnitude and breadth of HIV-1 Env-specific polyfunctional antibodies. Immunization with mRNA-LNP encoding Zika premembrane and envelope or HIV-1 Env gp160 induces durable neutralizing antibodies for at least 41 weeks. Doses of mRNA-LNP as low as 5 μg are immunogenic in macaques. Thus, mRNA-LNP can be used to rapidly generate single or multi-component vaccines, such as sequential vaccines needed to protect against HIV-1 infection. Such vaccines would be as or more immunogenic than adjuvanted recombinant protein vaccines in primates.
Messenger ribonucleic acid (mRNA)-based vaccines have been shown to elicit protective immunity against Zika virus (ZIKV) infection after a single immunization of rhesus macaques1, and have been designed for many other pathogens including Ebola, influenza, Hepatitis C, Cytomegalovirus, and respiratory syncytial virus2,3,4,5,6,7.
The recent development of mRNA vaccines has overcome initial roadblocks to their use. mRNA vaccines were initially hindered by innate immune sensing of mRNA7,8,9. However, advances in modifying mRNA nucleosides have improved mRNA translation, while eliminating recognition by innate pattern recognition receptors7,8,10. Specifically, the incorporation of pseudouridine and 1-methyl-pseudouridine prevents recognition of mRNA by Toll-like receptor 7 and 8 and other nucleic acid sensing pattern recognition receptors7. Modification of mRNA in combination with HPLC and FPLC purification methods and codon optimization methods have increased the efficiency of mRNA production and the efficacy of mRNA vaccination8,11,12. For mRNA to be effective at transducing cells in vivo, it must be protected from RNAses. One method for protecting the mRNA from degradation has been its encapsulation in lipid nanoparticles (LNP)7,8,13. Importantly, small interfering RNAs (siRNAs) in LNP have been approved by the FDA for the treatment of a genetic form of amyloidosis14. Thus, advances in encapsulation and preventing mRNA immune sensing have made mRNA vaccines a feasible vaccine platform.
mRNA vaccines are also attractive as a vaccine platform, because they can accept the genes of various pathogen antigens, and they can be rapidly manufactured at scale. These two aspects made mRNA vaccines a prime candidate for responding to the SARS-CoV-2 outbreak15,16. High levels of SARS-CoV-2 neutralizing antibodies, defined as higher than geometric mean values of convalescent serum from COVID-19 patients, were observed for both nucleoside-modified mRNA-LNP and Matrix-M1 adjuvanted subunit protein in human trials16,17,18. Given the ability of mRNA vaccines to elicit neutralizing antibodies8,16,17, this platform could improve the elicititation of neutralizing antibodies against HIV-1. However, little data exists on the comparative immunogenicity of mRNA-LNP and proteins in non-human primates. Thus, a key question for HIV-1 vaccine development is whether the immunogenicity of mRNA vaccines encoding HIV-1 immunogens, a poorly immunogenic protein that requires extensive post-translational modifications, is comparable to that of proteins that can be purified after in vitro production.
HIV-1 vaccines aiming to elicit protective antibody responses will likely need to elicit polyfunctional non-neutralizing effector antibodies (nnAbs) and/or broadly neutralizing antibodies (bnAbs)19,20. NnAbs are easy to induce and bind to the surface of virus-infected CD4+ T cells where they can mediate antibody-dependent cellular cytotoxicity (ADCC). However, their efficacy in protecting against HIV transmission or control of the disease in the setting of high transmission rates was called into question with the HVTN 702 ALVAC-C, gp120-C trial failing to show efficacy21,22. The only HIV-1 clinical trial to date to demonstrate any efficacy, RV144, induced nnAbs by immunizing with gp120 proteins derived from HIV-1 isolates A244 and MN23. Protection in that trial correlated with binding IgG to the second variable region on Env and ADCC, but the protective antibody response was not durable24.
In contrast to nnAbs, bnAbs are difficult to induce for many reasons including shielding of bnAb Env epitopes by glycans, the metastability of Env conformation, conformational masking of neutralizing epitopes25,26,27, host immune controls preventing bnAb development28,29, and the requirement for multiple highly improbable somatic mutations that are needed for the acquisition of antibody neutralization breadth30,31,32. mRNA immunization elicits antigen-specific follicular T helper cells, which are key for affinity maturation of antibodies in germinal centers33,34, and has been shown to correlate with bnAb development during natural infection35,36. Regardless of whether it is nnAbs or bnAbs targeted, the poor durability of HIV-1 Env antibody responses37, and the necessity of designing a vaccine that has multiple components for bnAb induction19,20 necessitates additional vaccine platforms that can maintain protective antibody levels.
Here, we compare the antibody responses in rhesus macaques induced by either HIV-1 Env-encoded as nucleoside-modified mRNA-LNP or the same vaccine candidate administered as an adjuvanted HIV-1 Env recombinant protein. In each comparison, mRNA-LNP administration induced equal or better immune responses as proteins. Moreover, mRNA-LNP vaccination encoding soluble HIV-1 Env trimers or ZIKV prM-E elicited durable neutralizing antibodies that were stable for ~1 year.
Both protein and mRNA vaccination elicited high titers of serum HIV-1 binding antibodies
We compared the immunogenicity of HIV-1 Env A244 gp120 lacking the first 11 N-terminal amino acids of gp120 (Δ11 gp120, as in the RV144 trial)38 administered as either nucleoside-modified mRNA-LNP or adjuvanted recombinant protein in rhesus macaques. We immunized two groups of five macaques with recombinant protein formulated in different adjuvants. One group of five macaques received A244 Δ11 gp120 formulated with the aluminum hydroxide adjuvant Rehydragel (Fig. 1a). This group mimicked the A244 Δ11 gp120 protein aluminum hydroxide (Rehydragel) formulation used in the RV144 ALVAC/B/E gp120 trial23. Adjuvants vary in their immunostimulatory strength; thus, in the second group of five macaques, we assessed the immunogenicity of the A244 Δ11 gp120 Env in combination with a liposomal adjuvant formulation composed of monophosphoryl lipid A (a TLR-4 agonist) and QS21 (ALFQ)39. In addition, two groups of macaques were immunized with nucleoside-modified mRNA-LNP encoding different forms of A244 Δ11 gp120. One group of macaques received A244 Δ11 gp120, whereas the other group received mRNAs encoding A244 Δ11 gp120 with a D368R mutation that disrupted the CD4 binding site (Fig. 1a). The purpose of the CD4 binding site knockout mutation was to determine whether Env binding to CD4+ T cells in vivo altered the immunogenicity of HIV-1 Env gp120. Macaques were immunized with either protein or mRNA-LNP at weeks 0 and 6 and antibody responses were followed for 18 total weeks (Fig. 1a).
Binding nnAbs to Env immunogens have been associated with protection in macaques from SHIV infection40,41. Thus, we first determined serum binding IgG elicited by each of the mRNA/LNP or protein groups. Regardless of the site of immunization, gp120-specific IgG titers in the macaque serum were detectable after a single immunization and continued to rise after the second immunization (Fig. 1b). mRNA-LNP elicited nearly identical serum IgG antibody titers as compared to macaques immunized with A244 Δ11 gp120 formulated with ALFQ (Fig. 1b). Comparison of mRNA-LNP that encoded wildtype gp120 versus CD4 mutated gp120 showed identical binding IgG elicitation (Fig. 1b). Macaques that received A244 Δ11 gp120 formulated with Rehydragel generated the lowest group mean serum IgG binding titers to A244 Δ11 gp120. For these ELISA assays, the differences between the Rehydragel group and the other groups were greatest after one immunization, but the small numbers of monkeys per group precluded statistical analysis. Nonetheless, ALFQ adjuvant-induced higher levels of A244 Δ11 gp120 antibody compared to gp120 in Rehydragel (Fig. 1b). The same group ranking was also observed for binding IgG to a HIV-1 Env gp120 B.63521 from a non-vaccine matched HIV-1 isolate (Fig. 1b). The binding of serum antibodies to A244 gp120 was not reduced by the introduction of mutations in the CD4 binding, glycan-V3, and glycan-V2 sites (Fig. 1b). Thus, mRNA-LNP gp120 vaccination produced comparable IgG titers in plasma as recombinant gp120 protein in the potent adjuvant ALFQ.
IgG responses to the second variable (V2) region of HIV-1 Env were a correlate of reduced infection risk in the RV144 trial24. Similarly, K169 in the V2 region was a site of immune pressure during the RV144 trial42. To assess whether nucleoside-modified mRNA-LNP vaccination elicited comparable V2 region IgG antibodies in plasma, we tested serum IgG binding to various minimal antigens that recapitulated the V2 region of HIV-1 Env. These antigens included V1V2 proteins, a V2 peptide, and V2 scaffolded on gp70. Binding to each antigen showed the same pattern as gp120 binding. Recombinant protein adjuvanted with AFLQ and mRNA-LNP immunization elicited nearly identical plasma IgG responses (Fig. 2). Recombinant gp120 adjuvanted with Rehydragel elicited the weakest responses for all the antigens tested, with group difference being largest after a single immunization (Fig. 2). V1V2-specific binding IgG titers were comparable whether the V1V2 antigen matched the vaccine strain or if it was from an unmatched virus 1086C (Fig. 2a). The first variable region (V1) was not necessary for V2 binding, as plasma IgG bound to a short V2 only peptide, K178 (Fig. 2b). The antigen for which binding IgG correlated with reduced infection risk in the RV144 trial was B.CaseA V1V2 scaffolded on gp7024,43. Each group of macaques generated binding IgG antibodies to gp70 B.CaseA V1V2 protein (Fig. 2c). The antibodies were specific for HIV-1 V1V2, as no antibodies were detected against the control gp70 scaffold presenting murine leukemia virus V1V2 (Fig. 2c). However, mutation of K169 had little effect on B.CaseA V1V2 binding IgG titers. Similarly, mutation of the K169 in the V2 region of A244 gp120 had little effect on binding IgG titers (Fig. 1b). Thus, V1V2 antibodies were not solely dependent on the K169 at the site of immune pressure observed in the RV144 trial.
To determine the breadth of reactivity and epitope specificity of the first and second variable (V1V2) region antibodies induced by each vaccine, we performed linear V1V2 peptide arrays. Vaccination induced only low levels of V1-binding antibodies, but high titers of V2 antibodies across the different vaccines (Fig. 3a–d and Supplementary Fig. 1). V2 antibody binding magnitudes were similar for mRNA-LNP and protein formulated with ALFQ (Fig. 3). Each vaccine-elicited antibodies capable of binding V2 peptides from clade AE and C (Fig. 3 and Supplementary Fig. 1). Therefore, mRNA-LNP and adjuvanted protein vaccination elicited V2 antibody responses that were similar in magnitude, breadth, and epitope specificity.
Next, we compared plasma antibody specificities induced by protein or mRNA-LNP immunization at HIV-1 Env gp120 sites outside of the V1V2 site. mRNA-LNP induced similar A244 gp120 linear epitope antibodies compared to protein formulated in adjuvant with two exceptions. First, recombinant protein, but not mRNA-LNP, elicited plasma IgG to the C-terminal portion of the second constant (C2) region (Fig. 3e–h and Supplementary Fig. 2). Second, mRNA-LNP immunization elicited plasma IgG against the third constant region but recombinant protein immunization did not (Fig. 3e–h and Supplementary Fig. 2).
To further compare polyclonal plasma IgG specificities, we assessed the ability of post-vaccination plasma to block the binding of gp120 monoclonal antibodies (mAbs) to HIV-1 Env. Plasma from either adjuvanted protein- or mRNA-LNP-immunized macaques was added to HIV-1 Env protein, followed by the addition of biotinylated mAbs to determine plasma antibody blocking of monoclonal antibody binding to Env. We examined blocking of nnABs CH58, which targets the V2 site of immune pressure identified in RV14444, and A32 which defines an immunodominant ADCC gp120 site45 that synergizes with V2 antibodies to mediate ADCC46 (Fig. 4a). Next, we determined whether plasma could block the HIV-1 entry receptor CD4 from binding to Env (Fig. 4b), or block V2-glycan bnAbs PG9 and CH01 and N332 glycan-dependent bnAbs 2G12 and PGT125 Env binding (Fig. 4c, d). Either immunization with adjuvanted recombinant gp120 protein or mRNA-LNP elicited plasma antibodies that blocked the binding of CH58, A32, CD4, CH01, 2G12, and PGT125 (Fig. 4). Comparison of mRNA-LNP-induced antibodies versus gp120 protein-induced plasma antibodies showed that mRNA-LNP immunization elicited the same magnitude of blocking after 2 immunizations as protein adjuvanted with ALFQ (Fig. 4). Blocking activity was lowest for animals immunized with protein adjuvanted with Rehydragel (Fig. 4). The blocking of CH01 binding to A244 most likely represented CH58-like antibody binding and not V2-glycan bnAb binding, since CH01 binding can be blocked by CH58-like linear V2 antibodies (Fig. 4).
Comparable neutralizing and non-neutralizing antibody functions induced by adjuvanted Env gp120 protein versus mRNA-LNP immunization
Several IgG Fc receptor (R)-mediated immune responses have been associated with decreased transmission risk either in the RV144 trial or in Env immunizations studies in macaques followed by low dose mucosal SHIV challenges41,47. These immune responses include binding to HIV-1 infected CD4+ T cells, ADCC, and antibody-dependent cellular phagocytosis (ADCP). To assess the potential for week 8 plasma IgG to mediate effector functions against infected cells, we first examined plasma IgG binding to HIV-1.CM235-infected T cells. Plasma IgG from all four groups of macaques was able to bind to HIV-infected cells (Fig. 5a, b). When binding levels of IgG was quantified as mean fluorescence intensity of bound IgG or the percentage of cells positive for HIV-1 protein p24 and plasma IgG, mRNA-LNP vaccination and recombinant protein adjuvanted with ALFQ were not different (Fig. 5a, b). In agreement with the overall lower IgG titers, Rehydragel-adjuvanted protein gave the weakest cell-binding responses (Fig. 5a, b).
ADCC activity was measured in a flow cytometry-based granzyme B assay. There was a clear adjuvant effect between the two protein-immunized group. ADCC titers were approximately one order of magnitude higher when ALFQ was used as the adjuvant as compared to Rehydragel. Similarly, mRNA-LNP immunization (mean ± standard deviation = 22,916 ± 22,102) induced activity lower than ALFQ-formulated recombinant protein, but threefold higher than protein adjuvanted with Rehydragel (mean ± standard deviation = 7324 ± 7024) (Fig. 5c). Elimination of CD4 binding to A244 Δ11 gp120 had no effect on ADCC activity (Fig. 5c). Lastly, we compared ADCP activity of week 8 plasma antibodies from macaques administered adjuvanted recombinant protein or mRNA-LNP. Median plasma ADCP activity against A244 gp120-coated beads was similar across all groups with A244 Δ11 gp120 in Rehydragel eliciting a wider range of responses (Fig. 5d). In agreement with previous studies, nucleoside-modified mRNA-LNP vaccination elicited antibody effector functions that have been shown previously to correlate with reduced infection risk24,48.
While the goal of A244 Δ11 gp120 immunization was to induce non-neutralizing effector functions like those seen in the RV144 trial, we compared elicitation of neutralizing antibodies by each of the vaccines. We selected for testing the tier 1 HIV-1 strain CRF_01AE 92TH023, against which A244 has consistently induced neutralizing antibodies24,44. We found that there was no significant difference among the different vaccination regimens for induction of HIV-1 92TH023 neutralizing antibodies (Supplementary Fig. 3). These studies showed that for immunization with gp120 monomers aiming to elicit potentially protective non-neutralizing V2 antibodies, nucleoside-modified mRNA-LNP vaccination was superior to recombinant protein formulated with aluminum hydroxide and comparable to recombinant protein formulated with a more complex TLR-4/QS21/liposomal adjuvant.
Immunizations of macaques with sequential CH505 Env gp160 mRNA-LNP, SOSIP gp140 mRNA-LNP, or adjuvanted recombinant SOSIP gp140 proteins
We previously isolated CD4 binding site bnAbs from the African individual CH50549,50. From CH505, we cloned a series of different CH505 Envs for testing as immunogens to induce similar types of bnAbs with vaccination49,50. To this end, we studied a mRNA-LNP sequential immunization strategy where each individual envelope in the series is delivered one-at-a-time in a specific order. The HIV-1 envelope immunogens were designed as transmembrane HIV-1 gp160s (50 μg/immunization) or soluble, stabilized gp140 SOSIP trimers (50 μg/immunization; Fig. 6a). The SOSIP gp140s were stabilized by a chimeric gp41 and the addition of E64K and A316W mutations51. The immunogenicity of these two sets of mRNA-LNP was compared to that of 100 μg of the same set of CH505 Envs as soluble gp140 SOSIP proteins formulated in the TLR-4 adjuvant, GLA-SE (Fig. 6a). Four rhesus macaques were immunized every four weeks with either set of immunogens (Fig. 6a), and binding antibody and neutralizing antibodies were measured.
All three vaccines were immunogenic in macaques. With regard to induction of binding titers of gp120 antibodies, mRNA-LNP encoding sequential CH505 gp160s induced higher gp120 titers than did either of the mRNA-LNP encoding soluble gp140 SOSIP trimers or soluble gp140 SOSIP trimers proteins (Fig. 6b). These binding titers rose dramatically after two immunizations with gp160 mRNA-LNP, but rose gradually over the course of five immunizations in macaques immunized with SOSIP gp140s (Fig. 6b). Plasma IgG binding titers to gp120 were equivalent between the mRNA-LNP and the adjuvanted soluble gp140 SOSIP trimer protein-immunized animals (Fig. 6b). Soluble gp120 exposes non-neutralizing epitopes, thus we examined whether the high titers of gp120 antibodies in macaques immunized with gp160 mRNA-LNP were due to antibodies targeting these sites. Indeed, the gp160 mRNA-LNP induced very high titers of antibodies to linear CH505 TF V2 peptides, whereas titers in the gp140 SOSIP trimer groups showed no or a slight increase from baseline (Fig. 6c). Linear V3 epitopes were also highly immunogenic in gp160 mRNA-LNP-immunized macaques, and to a lesser extent was immunogenic in soluble gp140 SOSIP trimer protein-immunized macaques (Fig. 6d). Interestingly, V3 antibodies were not elicited by gp140 SOSIP trimer mRNA-LNP, suggesting a difference in V3 exposure when the trimer was expressed in vivo or potential effects of the adjuvant. To examine the induction of gp120 antibodies that may target conserved neutralizing epitopes, we assessed the amount of gp120 antibody binding that was dependent on the CD4 binding site. We mutated the CD4 binding site with a deletion of the isoleucine at position 371 and determined the decrease in plasma IgG binding to CH505 TF gp120. Both groups of macaques that received SOSIP trimers as either protein gp140s or mRNA-LNP were superior to the mRNA-LNP encoding the gp160s (Fig. 6e). Immunization with gp140 SOSIP trimers elicited differential binding between the mutant and wildtype gp120 that rapidly receded after each immunization, but was maintained for 16 weeks once immunizations were stopped (Fig. 6e). Similar to linear V2 and V3 peptide antibodies, gp160 mRNA-LNP induced high levels of gp41 antibodies whereas gp140 SOSIP trimers delivered as mRNA-LNP or adjuvanted recombinant protein had levels close to baseline (Fig. 6f). Thus, gp160 mRNA-LNP immunization elicited higher titers of undesired antibodies targeting non-neutralizing gp120 and gp41 epitopes and lower titers of desired CD4 binding site antibodies than SOSIP trimer-encoding mRNA-LNP or adjuvanted recombinant protein. However, none of the regimens induced significant tier 2 or heterologous neutralizing antibodies due to the need for high-affinity germline B cell targeting and designs of sequential Env regimens that select for bnAb improbable mutations (Supplementary Tables 1–3)20,31,32,52,53.
The high levels of undesired antibodies elicited by gp160 mRNA-LNP immunization could be due to poorly folded HIV-1 envelope expressed on the surface of cells. We hypothesized that stabilization of HIV-1 envelope with amino acid substitutions that preserve Env trimers in their native conformation could reduce HIV-1 envelope binding to non-neutralizing antibodies. We introduced stabilizing amino acid changes H66A and A582T into envelope54. Also, we generated envelopes with G458Y and cysteines at positions 113 and 429 or 113 and 43155. The cysteines have been shown to form disulfide bonds that keep the HIV-1 envelope in the closed conformation55 and G458Y stabilizes the envelope fifth variable loop53. Among these variants of the M5 gp160 envelope, adding H66A and A582T reduced binding by non-neutralizing antibodies against V3 and gp41, while leaving trimer-specific (PGT145) or timer-preferring (PG9 and CH01) antibody binding unchanged (Fig. 6g). Thus, mRNA immunization with stabilized HIV-1 envelope gp160 is one potential approach to improve the elicitation of neutralizing antibodies, while not engaging the B cell receptor of B cells that produce antibodies that cannot bind native, fusion-competent HIV-1 envelope.
Nucleoside-modified mRNA-LNP immunization induces durable antibody responses against Zika prM-E and HIV-1 Env
Inducing durable Env antibody responses is a key goal of HIV vaccine development. Yet in the RV144 trial, protective antibodies fell dramatically over the first 42 weeks after vaccination24. Thus, if immunization with mRNA-LNP induced durable antibody responses it would benefit their use as a vaccine platform for many different infectious diseases. We assessed the durability of antibody responses using neutralization assays of tier 1 CH505 w4.3 virus, since antibodies capable of neutralization of the tier 2 CH505 transmitted founder (TF) virus were not elicited (Supplementary Tables 1–3). CH505 w4.3 is an early virus isolate that is identical to the tier 2 CH505 TF virus with the exception of a W680G mutation that makes it highly sensitive to HIV antibody neutralization49,56,57. Longitudinal comparative analyses of neutralization of the CH505 w4.3 virus showed that the gp160-encoding mRNA-LNP elicited higher titers of neutralizing antibodies than the gp140 SOSIP trimer-encoding mRNA-LNP or the gp140 SOSIP trimer proteins in GLA/SE58 (Fig. 7a). Notably, neutralization of the CH505 w4.3 virus was still detectable in all three groups 12 weeks after the last immunization (Fig. 7a). There were also sporadic low levels of neutralization of CH505 or 426 C viruses that were modified to be highly sensitive to CD4 binding site antibodies (Supplementary Tables 1–3).
While these results indicated that durable neutralizing antibodies were elicited by each vaccine regimen, the downward trend of the neutralization titers in these macaques and the A244-immunized macaques raised the question of how long would neutralizing antibodies persist at detectable levels. A subset of the macaques used in this HIV-1 study was previously administered 50 μg of mRNA-LNP encoding ZIKV pre-membrane and envelope (prM-E). These macaques generated protective anti-Zika neutralizing antibody responses1. Using these macaques that were administered both HIV and Zika mRNA-LNP vaccines, we determined serum neutralizing antibodies titers over 52 weeks (Fig. 7b). We found that neutralizing antibodies against ZIKV were maintained until the last timepoint of follow-up 52 weeks after immunization. Neutralizing antibodies to HIV-1 persisted for the duration of the 41 weeks of follow-up. During these 41 weeks, HIV-1 titers initially fell ~10-fold after the last immunization but plateaued at ~1:100 titer (Fig. 7b). In contrast, Zika neutralizing antibody levels were maintained at the same level for the 52 weeks after being detected at week 2 (Fig. 7b). Similar patterns were observed for plasma binding IgG titers to CH505 gp120 and Zika prM-E (Fig. 7c). Taken together, nucleoside-modified mRNA-LNP immunizations induced durable serum neutralizing antibodies for both HIV-1 and ZIKV.
Neutralizing antibody titers are dependent on mRNA-LNP dose
In our previous ZIKV vaccine studies in nonhuman primates, we administered 50, 200, or 600 μg of mRNA-LNP1. Given the potent elicitation of neutralizing antibodies by mRNA administered at each of these doses, we sought to determine whether the mRNA dose could be further decreased. We immunized four macaques intramuscularly with either 50, 20, or 5 μg of mRNA-LNP encoding Zika prM-E (Fig. 8a) and compared titers of binding IgG and neutralizing antibodies. Fifty and twenty microgram doses of mRNA-LNP elicited similar titers of binding IgG and neutralizing antibodies (Fig. 8b, c). Titers of ZIKV binding IgG and neutralizing antibodies were substantially decreased when the mRNA-LNP dose was lowered to 5 μg, but was detectable with the administration of this single administration of a small amount of mRNA-LNP in macaques. The route of immunization was not critical as administering 50 μg of mRNA-LNP either intramuscularly or intradermally elicited comparable Zika envelope binding IgG and Zika neutralizing antibodies (Fig. 8b, c). In summary, the mRNA-LNP dose could be lowered from 50 to 20 μg in macaques without detrimental effects to antibody responses. Thus, more immunizations can be performed with each preparation of mRNA-LNP by reducing the dose by 60 percent.
Here, we demonstrate in 28 rhesus macaques that immunization with nucleoside-modified mRNA-LNP (n = 16) was equal to or superior to the immunogenicity of adjuvanted Env protein. There are multiple factors for why nucleoside-modified mRNA immunization has potent immunogenicity for viral proteins. First, mRNA is delivered by LNP to dendritic cells and likely other immune cells that are able to activate naive T cells to respond to the vaccine immunogen59,60,61. Second, nucleoside-modified mRNA-LNP immunization generates robust antigen-specific germinal center T and B cell responses2. Within the germinal center, follicular T helper cells provide help to B cells undergoing affinity maturation34. The affinity maturation process is critical for the development of high-affinity antibodies after vaccination, and in particular for HIV-1 is required for bnAb development62. Animal models vaccinated with nucleoside-modified mRNA-LNP encoding HIV-1 Env or influenza virus hemagglutinin develop high levels of T follicular helper cells33. Given that HIV-1 neutralizing antibody breadth is correlated with the frequency of circulating T follicular helper cells35,36, nucleoside-modified mRNA-LNP immunization warrants further study as an HIV-1 vaccine platform. Nucleoside-modified mRNAs have many potential advantages over proteins including speed of production and cost-savings. Moreover, mRNA-LNP increases the feasibility of making under current good manufacturing practices the multicomponent vaccines that are needed to induce both protective HIV-1 bnAbs and nnAbs.
In RV144, aluminum hydroxide (Rehydragel) was used and poor durability of protective immune responses was observed24,63. ALFQ is a potent adjuvant that contains anionic liposomes, QS21, and TLR-4 agonist, MPL39, both potent adjuvants. Thus, comparison of mRNA-LNP with Rehydragel gives a direct indication of how it might fare versus the RV144 regimen, and comparison with ALFQ provides an indication of how it might fare in comparison with a stronger adjuvant. The adjuvant GLA (synthetic MPL) in SE (stable emulsion)58 has been used in HVTN 115 with multiple gp120s and was immunogenic, although in a head-to-head comparison of Rehydragel and GLA-SE in primates, they were similar in promoting immunogenicity except for V2 responses where Rehydragel was superior. While ALFQ and GLA stable emulsion contain lipids, they differ from the LNPs. The LNPs include ionizable cationic lipids that give the LNP a neutral surface charge, whereas most commercial liposomes lack ionizable cationic lipids. The neutral charge helps reduce non-specific protein binding in vivo. Unlike GLA or ALFQ, the LNP does not activate TLR-4, but instead activates follicular helper T cells33. In general, with the doses and adjuvants used in this study of proteins versus mRNA-LNP, nucleoside-modified mRNA-LNP immunization was superior or equal to protein in Rehydragel or GLA-SE and equal to protein in ALFQ. Future studies using different vaccination intervals, adjuvants, and protein doses could corroborate this conclusion.
There are currently two ongoing efficacy trials that test the protective capacity of non-neutralizing HIV-1 antibodies with viral vector prime, Env protein boosts to determine if the 42-month efficacy of ALVAC/gp120 can be replicated. In addition, the just-completed HVTN 702 trial (NCT02968849) uses an ALVAC with a clade C Env insert as prime and ALVAC-C + a bivalent C gp120 Env boost failed to confer any protection from HIV-1 infection in South Africa in an area of high HIV-1 infection rates. The ongoing HVTN 705 trial (NCT03060629) tests the efficacy of an adenovirus (Ad) 26 vector containing mosaic HIV-1 genes as a prime and the same Ad26 + a clade C gp140 Env as a boost, and the HVTN 706 trial (NCT03964415) tests the efficacy of Ad26 mosaic HIV as a prime and Ad26 + a bivalent clade C gp140 Env + a mosaic gp140 Env as boost64. The correlate of decreased transmission risk in macaque studies of the A26, Ad26 + gp140 boost SHIV challenge studies did not include neutralization breadth of antibodies, but instead included clade C Env ELISA binding antibodies and interferon-gamma Env ELISPOT values64. Thus, these latter two vaccines will test whether non-neutralizing antibody effector functions can mediate significant protection in humans.
The ease and cost-effectiveness of mRNA-LNP production compared to the production of multiple recombinant proteins by good manufacturing practice (GMP) techniques make mRNA-LNP particularly attractive. Furthermore, the scalability of mRNA-LNP for thousands to millions of doses again make the cost and ease of production of mRNA-LNP attractive. These manufacturing considerations are key for improving on RV144, and show great promise for COVID-19 vaccines currently under development17. However, the cold temperature required for the distribution and storage of mRNA vaccines remains a challenge for this vaccine platform65.
While mRNA vaccination is promising, there are still improvements that can be made for HIV mRNA-LNP vaccination. Specifically, for bnAb induction by mRNAs, the near-native Env trimers will need to be stabilized such that they will be able to be produced by the transfected cell in a well-folded state. This challenge is not unique to mRNA as DNA vaccination has also faced similar roadblocks66. This aspect of genetic vaccination differs from recombinant proteins that can be purified prior to immunization and recognition by the immune system. However, there are a plethora of available mutations for stabilizing HIV-1 envelope, and each envelope has different intrinsic stability that can be further augmented. We investigated only two potential sets and found H66A and A587T reduced non-neutralizing antibody binding to the envelope in vitro. The reduction in non-neutralizing antibody binding suggests a higher percentage of native-like envelope expressed by the mRNA. Future vaccine studies will need to determine whether reduced non-neutralizing antibody binding in vitro translates to improved neutralizing antibody elicitation in vivo. Despite the best envelope stabilization designs, it is possible that not all of the envelope will be well-folded, native-like trimers. In vivo studies by us and others are aiming to determine what the percentage of well-folded envelope needs to be in order to elicit optimal neutralizing antibody responses. Both of these important questions are areas of intense investigation and are critical for mRNA becoming a widely accepted HIV-1 vaccine platform.
In summary, comparison of nucleoside-modified mRNA-LNP with recombinant Env proteins in three adjuvants demonstrated the utility of mRNA-LNP as a mode of inducing nnAbs that are predicted to be protective against retrovirus challenge. We suggest that moving to nucleoside-modified mRNA-LNP for the next generation of clinical trials for multivalent Env immunization will be advantageous and speed the development of a globally available protective HIV-1 vaccine.
Animals and immunizations
Rhesus macaques were housed and treated in AAALAC-accredited institutions. The study protocol and all veterinarian procedures were approved by the Duke University IACUC and were performed based on standard operating procedures. Macaques were anesthetized with ketamine for immunizations and blood collection. For protein immunizations, rhesus macaques were immunized with 300 μg of A244 gp120 monomers in the quadriceps. In previous macaque studies, 300 μg and 100 μg of A244 gp120 monomers gave equivalent antibody responses. Thus, 100 μg of HIV-1 CH505 stabilized SOSIP gp140 recombinant protein were administered in the quadriceps of rhesus macaques instead of 300 μg. Total immunization volume was 1 mL of protein and adjuvant diluted in phosphate-buffered saline (PBS). For RNA immunizations, rhesus macaques were shaved on their backs and injected intradermally with nucleoside-modified mRNA-LNP diluted in PBS. For ZIKV immunization, three macaques received 600 μg and two macaques received 200 μg of mRNA expressing Zika preM-E1. In our previously published mRNA-LNP titration, there was no difference in antibody titers with 600, 200, and 50 μg of mRNA-LNP expressing Zika preM-E1; thus, for HIV-1 immunizations we administered 50 μg of mRNA-LNP expressing HIV-1 Env. Blood was collected by femoral venipuncture under ketamine anesthesia. Serum and EDTA-plasma were isolated from whole blood and stored at −80 °C1.
Production of recombinant Env protein immunogens
Recombinant HIV-1 Env gp120 was expressed in Freestyle 293-F cells (ThermoFisher) by transient transfection. To transfect Freestyle 293-F cells, 1 mg of plasmid DNA encoding HIV-1 Env per 1 liter of cells was diluted in DMEM and mixed with polyethyleneimine (PEI, Polysciences, Inc.). The DNA was allowed to complex with PEI for 25 min and then cells were added. The Freestyle 293-F cells were incubated with the PEI:DNA mixtures for 4 h. Freestyle 293-F (ThermoFisher) cells were subsequently centrifuged and resuspended in Freestyle293 media (ThermoFisher) at a final density of 1.25 million cells/mL. Four days after transfection, the cell culture media was cleared of cells by centrifugation and filtered with 0.8 μm filter. A Vivaflow 50 with a 10 kD MWCO (ThermoFisher) was used to concentrate the cell-free culture media. The concentrated cell culture supernatant was incubated with Galanthus Nivalis lectin beads (Vistar Laboratories) rotating overnight at 4 °C. The beads were pelleted by centrifugation the next day and resuspended in MES wash buffer (20 mM MES, 10 mM CaCl2, 130 mM NaCl pH7.0). The lectin beads were washed twice with MES wash buffer, and the protein was eluted with MES wash buffer supplemented with 500 mM methyl-alpha-D-mannopyranoside (Sigma). The protein was buffer exchanged into PBS by successive rounds of centrifugation and stored at –80 °C.
HIV-1 Env soluble trimers were designed as gp41-chimeric SOSIP gp140s67,68,69. The gp41-chimeric SOSIP gp140s were further stabilized by the addition of E64K and A316W mutations67. CH505 SOSIP gp140 Envs were expressed as previously described70. Freestyle293 cells (Invitrogen) were diluted to 1.25 × 106 cells/mL with fresh Freestyle293 media up to 1 L total volume. The cells were co-transfected with 650 μg of SOSIP expressing plasmid DNA and 150 μg of furin expressing plasmid DNA complexed with 293Fectin (Invitrogen). The cell culture supernatant clarified on day 6 and subjected to positive PGT145 antibody affinity chromatography. Eluted protein was concentrated down to 2 mL for size exclusion chromatography with a Superose6 16/600 column (GE Healthcare) in 10 mM Tris pH8, 500 mM NaCl. Fractions containing trimeric HIV-1 Env protein were pooled together, sterile-filtered, snap frozen, and stored at −80 °C.
mRNAs were produced as previously described71 using T7 RNA polymerase (Megascript, Ambion) on linearized plasmids encoding codon-optimized72 ZIKV prM-E (pUC-TEV-ZIKV prM-E-A101) from the strain H/PF/2013 (Asian lineage, French Polynesia, 2013, GenBank: KJ776791); gp160 HIV-1 Env: coCH505.M5 Env (pUC-TEV-coCH505.M5 Env-A101), coCH505.M11 Env (pUC-TEV-coCH505.M11 Env-A101), coCH505w0.30.20 Env (pUC-TEV-coCH505w0.30.20 Env-A101), coCH505w0.136.B18 Env (pUC-TEV-coCH505w0.136.B18 Env-A101), coCH505w0.20.14 Env (pUC-TEV-coCH505w0.20.14 Env-A101), coCH505w0.30.12 Env (pUC-TEV-coCH505w0.30.12 Env-A101); chimeric stabilized HIV-1 Envs: CH505M5chim.6R.SOSIP.664v4.1 Env (pUC-TEV-CH505M5chim.6R.SOSIP.664v4.1 Env-A101), CH505M11chim.6R.SOSIP.664v4.1 Env (pUC-TEV-CH505M11chim.6R.SOSIP.664v4.1 Env-A101), CH505w20.14chim.6R.SOSIP.664v4.1 Env (pUC-TEV-CH505w20.14chim.6R.SOSIP.664v4.1 Env-A101), CH505w30.12chim.6R.SOSIP.664v4.1 Env (pUC-TEV-CH505w30.12chim.6R.SOSIP.664v4.1 Env-A101), CH505w30.20chim.6R.SOSIP.664v4.1 Env (pUC-TEV-CH505w30.20chim.6R.SOSIP.664v4.1 Env-A101), CH505w136.B18chim.6R.SOSIP.664v4.1 Env (pUC-TEV-CH505w136.B18chim.6R.SOSIP.664v4.1 Env-A101); gp120 HIV-1 Envs: A244delta11 gp120 Env (pUC-TEV-A244delta11 gp120 Env-A101), A244delta11 K368R gp120 Env (pUC-TEV-A244delta11 K368R gp120 Env-A101). mRNAs were transcribed to contain 101 nucleotide-long poly(A) tails based on the DNA-encoded poly(A) tail sequence. One-methylpseudouridine (m1Ψ)-5′-triphosphate (TriLink) instead of UTP was used to generate modified nucleoside-containing mRNA. RNAs were capped using the m7G capping kit with 2′-O-methyltransferase (ScriptCap, CellScript) to obtain a type 1 cap. mRNA was purified by Fast Protein Liquid Chromatography (FPLC) (Akta Purifier, GE Healthcare), as described73. All mRNAs were analyzed by agarose gel electrophoresis and were stored frozen at −20 °C.
LNP formulation of mRNA
FPLC-purified m1Ψ-containing HIV-1 Env and ZIKV prM-E mRNAs were encapsulated in LNP using a self-assembly process in which an aqueous solution of mRNA at pH = 4.0 is rapidly mixed with a solution of lipids dissolved in ethanol74. LNP used in this study were similar in composition to those described previously74,75, which contain an ionizable cationic lipid (proprietary to Acuitas)/phosphatidylcholine/cholesterol/PEG-lipid. The proprietary lipid and LNP composition are described in US patent US10,221,127. They had a diameter of ~80 nm as measured by dynamic light scattering using a Zetasizer Nano ZS (Malvern Instruments Ltd, Malvern, UK) instrument.
In vitro mRNA transfection and flow cytometry
In vitro mRNA transfection and antibody binding were performed as earlier described76. Freestyle 293F cells were maintained at 37 °C with 8% CO2 and shaking at 130 rpm. Cells were diluted to 1 × 106 cells/ml prior to transfection. Bare mRNA encoding CH505 M5 gp160 Envs were transfected at 0.5 μg/million cells using TransIT-mRNA Transfection Kit (Mirus). Transfected cells were harvested 48 h post transfection. Cells were first incubated with HIV antibodies at 10 μg/ml for 30 min at 4 °C in dark. Antibody binding was then detected by Goat F(ab’)2 Anti-Human IgG - (Fab′)2 (PE) (used at 2.5 μg/ml) by incubating cells with the secondary antibody for 30 min at 4 °C in dark. Finally, data were collected on a LSRII with a high-throughput system.
HIV-1 Env direct ELISAs
Direct ELISAs were performed as stated previously77,78. Specifically, NuncSorp 384-well plates were coated with 30 ng (2 μg/mL) of antigen in 0.1 M sodium bicarbonate overnight at 4 °C. Plates were washed with SuperWash and blocked with SuperBlock. Plates were washed. Plasma was serially diluted in SuperBlock and added to the ELISA plate. The plate was washed twice and a 1:8000 dilution of anti-rhesus IgG conjugated to horseradish peroxidase (HRP; Rockland Immunochemicals) was incubated in the plate for 1 h. The plate was washed and tetramethylbenzidine (TMB; KPL) was incubated in the plate for 15 min to detect secondary antibody binding. The reaction was stopped with 1% HCl and absorbance at 450 nm was read with a SpectraMax plate reader (Molecular Devices). SoftMax Pro v5.3 was used to calculate log area-under-the-curve (AUC; Molecular Devices).
Plasma competition ELISAs
Plasma competition assays were performed as described previously77,78. In brief, NuncSorp plates were coated with HIV-1 Env, washed, and blocked as stated above for direct ELISAs. After blocking was complete, nonhuman primate plasma was diluted in SuperBlock at a 1:50 dilution and incubated in triplicate wells for 90 min. Non-biotinylated monoclonal antibodies were incubated with the Env in triplicate as positive controls for blocking. To determine relative binding no plasma or no antibody was added to a group of wells scattered throughout the plate. After 90 min the non-biotinylated antibody or plasma was washed away and biotinylated monoclonal antibodies was incubated in the wells for 1 h at subsaturating concentrations. Specifically, biotinylated monoclonal antibody concentrations used for binding to A244 Δ11 gp120 were: 0.04 μg/mL of CH58, 0.1 μg/mL of A32, 1.9 μg/mL of 2G12, 0.2 μg/mL of PGT125, 1.2 μg/mL of CH01, 1 μg/mL of PG9. Biotinylated CH01 and PG9 concentrations used for binding to 9021 gp140 and B.6240 Δ11 gp120 were 1.5 and 0.125 μg/mL respectively. For CD4 blocking assays, soluble CD4 was added followed by biotinylated anti-CD4 monoclonal antibody. Each well was washed and the binding of biotinylated monoclonal antibodies was determined with a 1:30,000 dilution of HRP-conjugated streptavidin (ThermoFisher). HRP was detected with TMB and stopped with 1% HCl. The absorbance at 450 nm of each well was read with a Spectramax plate reader (Molecular Devices). The binding of the biotinylated monoclonal antibody to HIV-1 Env in the absence of plasma was compared to in the presence of plasma to calculate percent inhibition of binding. Based on historical negative controls, assays were considered valid if the positive control antibodies blocked >20% of the biotinylated antibody binding.
HIV-1 Env peptide array
Peptide arrays were performed as previously described79. The HIV-1 peptide libraries contain overlapping HIV-1 peptides covering full-length gp120 of 5 consensus viruses from group M and clades A, B, C, and D79. Array slides were provided by JPT Peptide Technologies GmbH (Germany) by printing a library of peptides onto epoxy glass slides (PolyAn GmbH, Germany). The library contains overlapping peptides (15-mers overlapping by 12) covering five full-length gp160 consensus sequences (clade A, B, C, D, and group M). V3 peptide-binding breadth was analyzed for a library of V3 peptides (15-mers overlapping by 12) for seven consensus sequences (clade A, B, C, D, CRF1, and CRF2, and group M) and six vaccine strains (MN, A244, TH023, TV-1, ZM651, 1086C). Three identical subarrays were blocked for 1 h, followed by a 2-h incubation with monoclonal antibody, and subsequent 45-min incubation with anti-monkey IgG conjugated with AF647 (Jackson ImmunoResearch, PA). Slides were washed before the addition of monoclonal antibody or anti-monkey IgG. Unbound anti-monkey IgG conjugated with AF647 was washed away, and array slides were scanned at a wavelength of 635 nm using an InnoScan 710 scanner (InnopSys, Denmark) and images were analyzed using Magpix V8.1.1.
Antibody-dependent cellular cytotoxicity (ADCC)
ADCC activity was measured by ADCC GranToxiLux (GTL)80 and tested against subtype AE HIV-1 recombinant A244 ∆11 gp120-coated cells. NHP plasma was incubated with human PBMC as a source of effector cells81 and gp120-coated target CEM.NKR.CCR5 cells82 and ADCC was quantified as net percent granzyme B activity, which is the percent of target cells positive for GranToxiLux (GTL) detected by flow cytometry. For each subject at each timepoint, percent granzyme B activity was measured at six dilution levels: 50, 250, 1250, 6250, 31,250, and 156,250 for each antigen. Peak activity <0% was set to 0%. A positive response was defined as peak activity ≥8%. The RSV-specific monoclonal antibody Palivizumab and a cocktail of HIV-1 monoclonal Abs (A32, 2G12, CH44, and 7B2) were used as a negative and positive control, respectively. The potency of ADCC responses was evaluated by calculating the area under the curve using the non-parametric trapezoidal method.
Infected cells Ab binding assay (ICABA)
The measurement of plasma Ab binding to HIV-1 Env expressed on the surface of infected cells was conducted using flow-cytometry-based indirect surface staining according to methods similar to those previously described41,83. Briefly, mock infected and the subtype AE HIV-1 CM235-infected (HIV-CM235-2.LucR.T2A/293T/17, Accession Number AF259954.1) CEM.NKRCCR5 cells82 were incubated with 1:100 dilutions of plasma samples collected from the animals before immunizations and 2 weeks after the second immunization (week 8) for 2 h at 37 °C, then stained with a vital dye (Live/Dead Aqua) to exclude dead cells from analysis. The cells were subsequently washed, and permeabilized using BD Cytofix/Cytoperm solution. After an additional wash, cells were stained with FITC-conjugated goat-anti-Rhesus polyclonal antisera (Southern Biotech) to detect binding of the plasma Ab (pAb), and RD1-conjugated anti-HIV-1 p24 (KC57, Beckman Coulter) to identify infected cells. Background signal was defined as the signal obtained when staining cells with the secondary antibody alone, and signal observed when staining the mock-infected cells. Cells scored as positive for NHP plasma binding were defined as viable, p24 positive, and FITC positive. Final results are reported as the percent of FITC positive cells (p24 + pAb+) and FITC MFI among the viable p24 positive events after subtracting the background. Baseline correction for the FITC MFI was performed by subtracting pre-immunization MFI wherever applicable.
Phagocytosis was measured as stated previously84,85. Briefly, recombinant A244 Δ11 gp120 was incubated with 1 μM fluorescent beads overnight at 4 °C while rotating. The beads were subsequently washed twice with 0.1% BSA/PBS to remove unbound gp120. gp120-coated beads were incubated with prevaccination and postvaccination plasma for 2 h at 37 °C. As a positive control HIVIG was incubated with the beads. As a negative control monoclonal antibody CH65 was incubated with the beads, since this antibody reacts with influenza hemagglutinin and not HIV-1 Env. THP-1 or monocytes were incubated with anti-CD4 antibody SK3 (Biolegend) and then added to the bead/plasma mixture. The mixture was spinoculated for 1 h at 4 C followed by another 1 h incubation at 37 °C86. The cells were washed and fixed and fluorescence due to bead internalization was measured by flow cytometry. Positive phagocytosis was determined by two criteria. First, values at week 84 were considered positive if they were 3 standard deviations above values obtained in the prevaccination sample from the same macaque. Second, values obtained at week 84 had to be >3-fold higher than the prevaccination sample from the same macaque.
Neutralization assays were performed in TZM-bl cells using 293T-produced Env-pseudotyped viruses in a 96-well format as described87. Neutralization titers are the serum dilution at which relative luminescence units (RLUs) plotted on a non-linear regression curve were reduced by 50% compared to virus control wells after subtraction of background RLUs in uninfected cell control wells.
ELISA binding of plasma IgG to Zika E protein
ELISA binding was performed as described previously88. ZIKV envelope or HIV-1 proteins were coated overnight at 4 °C on the wells of 384-well plates (Corning Life Sciences). Each protein was coated at 2 μg/mL in 15 μl in sodium bicarbonate. Each well of the plate was blocked with assay diluent (PBS containing 4% [wt/vol] whey protein–15% normal goat serum–0.5% Tween 20–0.05% sodium azide) for 2 h at room temperature. Blocking solution was aspirated from each well and 10 μL of serially diluted macaque sera were added to the plate and incubated for 90 min. The plate was washed with PBS-Tween-20. Ten microliters of horse radish peroxidase anti-macaque IgG Fc were added to each well of the plate and incubated for 1 h. Subsequently, the plate was washed with PBS-Tween-20 and 30 μL of SureBlue substrate was used to visualize the presence of horse radish peroxidase. After 5–15 min the reaction was stopped with 15 μL of 0.1 M HCl. Absorbance at 405 nm was read for each well using a VersaMax microplate reader (Molecular Devices). Binding titers observed for the prevaccination timepoint were subtracted from the post vaccination timepoint for macaques that were part of mRNA-LNP dose study.
ZIKV MR-766 plaque reduction neutralization tests (PRNT). Serum neutralization was assessed as detailed previously1. Fifty plaque-forming units of ZIKV strain MR-766 (African lineage, Uganda, 1947, GenBank: AY632535) (UTMB Arbovirus Reference Collection) were incubated with increasing dilutions of heat-inactivated sera in serum-free DMEM (Corning) medium for 1 h at 37 °C. The virus/serum mixture was added to a confluent monolayer of Vero cells for 1.5 h at 37 °C with intermittent rocking. Three ml of overlay, containing a final concentration of 0.5% methylcellulose (4000 centipoise) (Sigma), 1× DMEM (Gibco), 16 mM HEPES, 0.56% sodium bicarbonate, 1.6× GlutaMAX (Gibco), 1× penicillin/streptomycin (Corning), and 4 μg/ml amphotericin B (Gibco), was added to each well. Plates were incubated for 5 days at 37 °C in 5% CO2. After incubation, the overlay was aspirated, cells were fixed and stained with 0.5% crystal violet (Sigma) in 25% methanol, 75% deionized water, rinsed with deionized water, and plaques inspected. Neutralization titers (EC50) were calculated as the reciprocal dilution of sera required for 50% neutralization of infection. EC50 titers below the limit of detection are reported as half of the limit of detection.
Zika reporter virus particle (RVP) neutralization assay. RVP neutralization assays were performed as described elsewhere1. RVPs were diluted to ensure antibody excess at informative portions of the antibody dose-response curve and incubated for 1 h at 37 °C with serial dilutions of heat-inactivated macaque sera to allow for steady-state binding. Serum-RVP mixtures were subsequently mixed with Raji-DCSIGNR cells at 37 °C. Each serum sample was tested in technical replicates. Every assay was repeated in two biologically independent assays. GFP-positive infected cells were detected by flow cytometry 24–48 h later. The EC50 was estimated using a non-linear regression with a variable slope (GraphPad Prism). The initial dilution of sera (based on the final volume of RVPs, cells, and sera) was set as the limit of quantification of the assay. EC50 titers below the limit of quantification were reported as a titer half the limit of quantification.
Descriptive statistics were calculated and reported for each assay. Group means, standard error, and geometric means were calculated with GraphPad Prism 8. Log AUC was calculated by Softmax Pro. EC50 titers for RVP neutralization were analyzed by non-linear regression to estimate the reciprocal dilution of sera required for half-maximal neutralization of infection (EC50 titer). The geometric mean of duplicate RVP neutralization EC50 titers were calculated using GraphPad Prism 8.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
The authors declare that the data supporting the findings of this study are available within the main and supplemental figures. All data are available from the corresponding author upon reasonable request.
No new code was generated in this study.
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We acknowledge technical assistance from Haiyan Chen, Esther Lee, Kedamawit Tilahun, Andrew Foulger, Aja Sanzone. This work was supported by NIH Division of AIDS UM1 grant AI100645 for the Center for HIV/AIDS Vaccine Immunology-Immunogen Discovery (CHAVI-ID; B.F.H.), NIH NIAID Duke Center for AIDS Research grant P30 AI064518 (S.X.S. and G.D.T.), and the intramural program of NIAID. The funders had no role in data collection and interpretation, or the decision to submit the work for publication.
The authors declare no financial conflicts of interest. B.F.H. and K.O.S. have patent applications submitted on CH505 Envs used in this study. T.C.P. is an inventor on multiple patent applications related to ZIKV vaccine antigen constructs and vaccines. In accordance with the University of Pennsylvania policies and procedures and our ethical obligations as researchers, we report that D.W. is named on patents that describe the use of nucleoside-modified mRNA as a platform to deliver therapeutic proteins. D.W. and N.P. are also named on a patent describing the use of nucleoside-modified mRNA in lipid nanoparticles as a vaccine platform. We have disclosed those interests fully to the University of Pennsylvania, and we have in place an approved plan for managing any potential conflicts arising from licensing of our patents.
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Saunders, K.O., Pardi, N., Parks, R. et al. Lipid nanoparticle encapsulated nucleoside-modified mRNA vaccines elicit polyfunctional HIV-1 antibodies comparable to proteins in nonhuman primates. npj Vaccines 6, 50 (2021). https://doi.org/10.1038/s41541-021-00307-6
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