The use of lipid-formulated RNA vaccines for cancer or COVID-19 is associated with dose-limiting systemic inflammatory responses in humans that were not predicted from preclinical studies. Here, we show that the ‘interleukin 1 (IL-1)–interleukin 1 receptor antagonist (IL-1ra)’ axis regulates vaccine-mediated systemic inflammation in a host-specific manner. In human immune cells, RNA vaccines induce production of IL-1 cytokines, predominantly IL-1β, which is dependent on both the RNA and lipid formulation. IL-1 in turn triggers the induction of the broad spectrum of pro-inflammatory cytokines (including IL-6). Unlike humans, murine leukocytes respond to RNA vaccines by upregulating anti-inflammatory IL-1ra relative to IL-1 (predominantly IL-1α), protecting mice from cytokine-mediated toxicities at >1,000-fold higher vaccine doses. Thus, the IL-1 pathway plays a key role in triggering RNA vaccine-associated innate signaling, an effect that was unexpectedly amplified by certain lipids used in vaccine formulations incorporating N1-methyl-pseudouridine-modified RNA to reduce activation of Toll-like receptor signaling.
For adjuvanted vaccines, induction of an innate immune response is essential to generate a protective, long-lasting adaptive immune response. Capable of eliciting exceptionally strong T cell responses1,2,3, RNA has emerged as an attractive vaccine platform not only for cancer therapy, but also for prophylaxis against infectious diseases such as COVID-19 (refs. 2,3,4,5,6). RNA-based vaccines activate a range of pattern recognition receptors (PRRs) due to their resemblance to infectious pathogens, thus mobilizing both adaptive and innate anti-viral mechanisms7. As a result, RNA vaccines induce systemic elevation of pro-inflammatory cytokines and dose-dependent, transient systemic reactions such as fever and chills1,2,3,4,5,6,8,9. These adverse events have been observed irrespective of administration route (intravenous (i.v.) or intramuscular delivery), formulation (liposomes or lipid nanoparticles (LNPs)) or RNA modifications (unmodified uridine or N1-methyl-pseudouridine, which reduces activation of Toll-like receptors 7 and 8 (refs. 10,11)).
In contrast to humans, C57BL/6 and Balb/c mice are remarkably tolerant to RNA vaccines and only display limited systemic cytokine release following i.v. administration of a liposomal vaccine containing unmodified RNA (RNA-LPX)1,12. Even at doses of RNA (50 µg) that are well tolerated in mice, patients exhibit transient mild-to-moderate flu-like symptoms that constrain dose exploration to a narrow range and possibly limit optimal T cell responses2,4,5. Given the obvious size differences, this means that RNA-LPX doses that trigger potent systemic inflammatory responses in humans are more than 1,000-fold lower than in inbred laboratory mice2. Similar observations have been made with other pro-inflammatory stimuli, creating a notable discrepancy in the dose needed to induce biological and toxicological responses in different species1,13,14. The mechanisms underlying these dramatic differences have remained largely unknown.
We investigated the ability of lipid-formulated RNA vaccines to trigger innate immunity. We uncovered the key role of IL-1 in triggering the release of other pro-inflammatory cytokines associated with cytokine release syndrome (CRS), with humans being markedly more sensitive than mice. Unlike humans, mice preferentially upregulated anti-inflammatory IL-1ra relative to IL-1, protecting them from uncontrolled systemic inflammation. Surprisingly, the reactogenicity of RNA vaccines was not necessarily due to the TLR7/8 agonism, as IL-1 release was observed using vaccines containing N1-methyl-pseudouridine-modified RNA (modRNA). Instead, the lipid components used to formulate these vaccines substituted for unmodified RNA in eliciting the IL-1 response.
RNA-LPX activates NLRP3 in monocytes
To identify the factors that contribute to sensitivity to innate immune stimuli, we first studied the unmodified RNA-LPX cancer vaccine, which encodes inherent TLR7/8 agonist activity1,12. Following RNA-LPX challenge on human peripheral blood mononuclear cells (PBMCs), a broad range of cytokines was detected in both total PBMCs and CD14+ monocytes; a notable reduction in cytokine secretion was seen in CD14-depleted PBMCs, indicating that the RNA-LPX-induced cytokine response was dependent on monocytes (Fig. 1a,b and Extended Data Fig. 1a,b). The production of IL-1β prompted us to ask if RNA-LPX activated the inflammasome pathway. Cotreatment of primary human monocytes with the NLRP3 inhibitor MCC950, the gasdermin D inhibitor necrosulfonamide or the pan-caspase inhibitor zVAD-FMK abolished the release of RNA-LPX-induced IL-1β (Fig. 1c,d,e), indicating that RNA-LPX-induced, monocyte-derived IL-1β release was dependent, as expected, on inflammasome and caspase activity.
Optimal activation of the canonical NLRP3 inflammasome requires two signals15,16. We reasoned that synthesis of pro-IL-1β (signal 1) was primed by TLR7/8 recognition of unmodified RNA, while NLRP3 inflammasome activation (signal 2) was triggered by the liposomes themselves. Indeed, modifying the RNA by substituting uridine with pseudouridine and cytosine with 5-methyl-cytosine (pseudoU5mC) which renders the RNA poorly recognizable by TLR7/8 (ref. 10) or administration of RNA-free liposomes (loss of signal 1) diminished the release of IL-1β (Fig. 1f). Similarly, the TLR7/8 agonist R848 alone failed to elicit IL-1β, while adding R848 with empty liposomes or pseudoU5mC-modified RNA-LPX resulted in readily detectable but lower IL-1β release compared with unmodified RNA-LPX (Fig. 1f).
Both unmodified and modified RNA-LPX also induced a robust generation of mitochondrial reactive oxygen species (ROS) in human monocytes (Fig. 1g). Notably, inhibition of mitochondrial ROS production using diphenyleneiodonium (DPI) or blockade of intracellular Ca2+ elevation using cell-permeable calcium chelator BAPTA-AM drastically reduced RNA-LPX-induced IL-1β release (Fig. 1h). This suggests that cationic liposomes (composed of the broadly used lipids DOTMA and DOPE) provide signal 2 by inducing mitochondrial ROS-mediated calcium influx17, possibly secondary to transient disruption of endosomal or plasma membranes18. The RNA-LPX complex can thus provide both signals 1 and 2 (Fig. 1i) which are required for efficient NLRP3 activation and IL-1β release from human monocytes in culture.
RNA-LPX induces IL-1 release in vivo
To determine if the in vitro findings were relevant to in vivo observations, we analyzed pre- and post-treatment plasma levels of IL-1β in a cohort of nine patients with cancer receiving RNA-LPX (autogene cevumeran) in a phase 1b study (NCT03289962). Following i.v. bolus injection of 25 µg of RNA-LPX, increase in circulating IL-1β was detected in 9 out of 9 patients to varying degrees, peaking at 4–6 h (Fig. 1j). In C57BL/6 mice, i.v. injection of RNA-LPX was also found to induce an elevation in the circulation of both IL-1β and IL-1α (Extended Data Fig. 2a,b). Although IL-1β expression was mainly observed in splenic Ly6Clo monocytes and neutrophils in the injected mice (Extended Data Fig. 2c,d,g), IL-1α was produced by Ly6Chi monocytes and red pulp macrophages (Extended Data Fig. 2e,f,g). Thus, both humans and mice upregulate IL-1 expression in monocyte/macrophage-lineage cells following RNA-LPX challenge.
IL-1α and IL-1β are important mediators of inflammatory responses well known to induce a MyD88-dependent signaling cascade upon binding to IL-1 receptor type 1 (IL-1R1)19,20. We next investigated the functional hierarchy of IL-1 cytokines in the context of innate immune stimulation (Fig. 2a). In the presence of IL-1β neutralizing antibodies, the RNA-LPX-induced cytokine secretion by human PBMCs was completely or almost completely blocked (Fig. 2b,c). Thus, the expression and release of IL-1β appeared to control the induction of most pro-inflammatory cytokines, including TNF and IL-6 (Fig. 2c). TNF blockade did not significantly reduce IL-6 release, nor did an anti-IL-6 antibody reduce TNF release (Extended Data Fig. 3a), indicating that cytokine release secondary to innate stimulation by RNA-LPX was mechanistically distinct from the CRS cascade initiated by T cell-activating therapies, where anti-TNF and anti-IL-6 are both effective inhibitors of the cytokine response21,22,23. Of note, out of all of the cytokines and chemokines screened, only CCL5 (also known as RANTES) was upregulated following IL-1β blockade, suggesting that IL-1 signaling negatively regulates the induction of CCL5 (Fig. 2b,c).
Systemic cytokine levels following RNA-LPX treatment were also significantly attenuated in IL-1R1-deficient (Il1r1−/−) mice as compared with wildtype mice both in vitro (Extended Data Fig. 3b,c) and in vivo (Fig. 2d,e). Consistent with our human data, in mice RNA-LPX-induced IL-1R1 signaling occurred upstream of IL-6 and TNF release, although the effect on TNF was less pronounced in the knockouts (Fig. 2e and Extended Data Fig. 3c). In contrast to Il1r1−/− mice, RNA-LPX administration did not result in a decreased serum cytokine response in NLRP3-deficient (Nlrp3−/−) mice (Extended Data Fig. 4a,b) or in gasdermin D-deficient (Gsdmd−/−) mice (Extended Data Fig. 4c,d). This finding can be understood from the fact that in mice, RNA-LPX also elicited the release of ~40-fold more IL-1α as compared with IL-1β (Extended Data Fig. 2b). IL-1α can activate IL-1R1 signaling independently of inflammasomes20, but nevertheless still controls the systemic cytokine response in mice (as opposed to IL-1β in human cells). Taken together, IL-1 appears to have a critical determinative role in amplifying cytokine responses initiated by innate immune stimuli both in humans and in mice.
IL-1 induction hierarchy varies between species
Due to its highly pro-inflammatory potential, the IL-1 signaling pathway is tightly regulated by soluble IL-1R1 as well as soluble and membrane forms of IL-1 receptor 2 (IL-1R2), each of which act as ligand traps or ‘decoys’20. Additionally, IL-1ra, a secreted anti-inflammatory cytokine, competes with active IL-1 and blocks binding to their common activating receptor, IL-1R1 (refs. 24,25,26). We first asked if IL-1ra production might play a role in modulating the activity of IL-1 induced by RNA-LPX by determining the amounts of IL-1α, IL-1β and IL-1ra released from human PBMCs. At lower dose levels of RNA-LPX (<2 µg ml−1), IL-1β and IL-1ra were released in nearly equivalent amounts (Fig. 3a). However, at higher RNA-LPX doses, the release of IL-1β markedly increased (~10-fold), greatly exceeding the release of IL-1ra, which remained constant (Fig. 3a). Thus, the ‘buffering capacity’ of IL-1ra is likely to be overcome as the degree of innate stimulation is increased. Of note, IL-1α levels remained low at all RNA-LPX dose levels in human cells (Fig. 3a).
Since mice are much less sensitive to RNA-LPX than humans (Extended Data Fig. 5a,b), we next asked if a similar IL-1 induction hierarchy occurred in mice. In stark contrast to human cells, IL-1ra was already highly released by murine leukocytes at baseline and further increased upon RNA-LPX; induction of IL-1α and IL-1β was only observed at high dose levels (Fig. 3b). We then treated C57BL/6J mice with RNA-LPX in vivo (Fig. 3c). While treatment with RNA-LPX induced a >10-fold upregulation of IL-1β and IL-1α, serum levels of IL-1ra were similarly induced and remained in ~100-fold molar excess over IL-1β and 10-fold excess over IL-1α (Fig. 3c, left panel). Qualitatively similar results were obtained from C57BL/6J mouse spleen (Fig. 3c, right panel) and from the serum of other sub-strains of C57BL/6 and Balb/c wildtype mice regardless of vendor origin or strain (Extended Data Fig. 5c).
To compare IL-1β versus IL-1ra release in vivo, we calculated the fold induction of systemic cytokine levels in C57BL/6 mice and in the nine patients with cancer from the phase 1b study, both groups having been treated with comparable absolute amounts of RNA-LPX. As expected based on the in vitro data, human patients treated with a tolerated dose of 25 μg showed a slight increase in induction of IL-1β over IL-1ra, whereas in mice, IL-1ra was dramatically induced relative to IL-1β (Fig. 3d). Of note, rather than normalizing RNA-LPX doses per animal weight, mice were administered identical absolute amounts of RNA-LPX as human patients (25 μg per injection). These findings suggest that IL-1ra can attenuate the effect of IL-1β in humans but only at low-to-moderate doses of RNA-LPX, while the substantial induction of IL-1ra would be expected to provide a far higher degree of attenuation against increases in IL-1α/β release in mice.
We also measured the respective cytokine levels in nonhuman primate (NHP) cells, as cynomolgus macaques and rhesus macaques are often used to assess safety and immunogenicity of RNA vaccines27. Interestingly, robust upregulation of IL-1ra was detected at all RNA-LPX dose levels, while IL-1β concentration and monocyte frequency were found to be lower in both cynomolgus macaque and rhesus macaque PBMCs compared with human PBMCs (Extended Data Fig. 5d–f). These results suggest that similar to mice, preclinical studies in NHPs might not fully capture the inflammatory toxicities related to RNA vaccines.
IL-1ra is the primary regulator of responses to RNA-LPX
To test directly whether the high systemic levels of IL-1ra explained the marked difference in tolerability between humans and mice, we administered RNA-LPX to IL-1ra-deficient (Il1rn−/−) mice and wildtype littermates. As observed previously, high-dose RNA-LPX (100 μg) was well tolerated in wildtype mice without any detectable adverse events. In contrast, RNA-LPX-treated Il1rn−/− mice rapidly developed a CRS-like phenotype characterized by pronounced hypothermia (Fig. 3e), body weight loss (Fig. 3f) and excessive systemic cytokine release (Fig. 3g). Notably, these adverse events were transient and resolved within days, similar to observations in human patients2,4,5. In the absence of IL-1ra, a marked increase in a wide range of pro-inflammatory cytokines was observed in systemic circulation (Fig. 3g). In addition, Il1rn−/− mice upregulated acute phase proteins such as serum amyloid A3 (SAA3), the murine equivalent to the human C-reactive protein (Fig. 3g). These differences could only be detected following RNA-LPX administration, as no differences in systemic cytokines were observed at baseline (Extended Data Fig. 6).
As neutrophilia was detected in untreated Il1rn−/− animals (Extended Data Fig. 6a–c), we decided to test whether the increased neutrophil count could be driving the exacerbated systemic cytokine responses. To this end, mice were pretreated with two doses of depleting anti-Ly6G antibodies before RNA-LPX administration (Extended Data Fig. 7a). Surprisingly, the depletion of Ly6G+ cells led to a moderate increase in RNA-LPX-induced IL-6 in Il1rn−/− mice but not in wildtype littermates (Extended Data Fig. 7b). This may be explained by an induction of cell-surface IL-1R2 on neutrophils in Il1rn−/− mice following RNA-LPX exposure (Extended Data Fig. 7c), suggesting a similar IL-1 inhibition mechanism as seen previously in humans28.
To fully assess the importance of the myeloid compartment on the magnitude of systemic inflammatory response, we also pretreated wildtype and Il1rn−/− mice with nine daily doses of murine FMS-like tyrosine kinase 3 ligand (Flt3L) (Extended Data Fig. 7d), which induces expansion of splenic macrophages, monocytes, dendritic cells and neutrophils29. Following i.v. administration of 50 μg of RNA-LPX, a markedly enhanced systemic cytokine response was observed in Flt3L-pretreated Il1rn−/− mice (Extended Data Fig. 7e), leading to lethal inflammation in 66% of these animals by 24 h post-vaccination. Interestingly, similar toxicities were not observed in Flt3L-pretreated wildtype animals, likely due to augmented induction of IL-1ra (Extended Data Fig. 7e). Altogether, these results show that endogenous IL-1ra can suppress IL-1-induced adverse events in mice and explain their tolerability to high doses of RNA-LPX.
In addition to contributing to the reactogenicity of the vaccine, IL-1 has been reported to serve as an innate instructor of adaptive immunity30. To study the role of IL-1 in vaccine-induced T cell responses, we injected Il1rn−/− and wildtype littermate mice with weekly doses of 2 μg, 10 μg or 50 μg of RNA-LPX vaccines encoding for seven previously characterized MC38 tumor neoantigens31 (Fig. 4a). While a dose-dependent expansion in total and neoantigen-specific T cells in blood was observed in both genotypes over time, markedly higher T cell counts were recorded in vaccinated IL-1ra-deficient mice compared with wildtype mice (Fig. 4b,c). Alternatively, lower doses or fewer vaccinations of RNA-LPX were required to induce comparable T cell responses in the absence of IL-1ra (Fig. 4c). To further assess the quality of the vaccine-induced T cells, we collected spleens 7 d after the final immunization for flow cytometric characterization. Analysis of T cell differentiation markers suggested that neoantigen-specific T cells exhibited a memory precursor effector cell (that is, CD127+ KLRG1−) phenotype in the absence of IL-1ra, while a higher proportion of vaccine-induced T cells in wildtype mice were short-lived effector cells (that is CD127− KLRG1+) following three vaccinations with 10 μg or 50 μg of RNA-LPX (Fig. 4d,e). We also observed a significant down regulation of TCF1 in splenic tetramer+ memory precursor effector cells in Il1rn−/− mice on day 19 (Fig. 4e), consistent with the robust T cell expansion in blood on day 18 (Fig. 4b,c) and enhanced polyfunctionality in spleen following peptide re-stimulation on day 19 (Fig. 4f). Thus, our findings indicate that even if limited by the antigen dose, unmodified RNA vaccines represent an effective approach to induce antigen-specific T cell responses when sufficient innate stimulus is provided, as suggested by clinical data1,2,4,5.
IL-1ra controls systemic responses to inflammatory stimuli
Given that excessive systemic inflammatory responses are commonly observed in human pathologies ranging from sepsis to viral infections, we asked if the regulatory role of IL-1ra could be generalized to other types of innate immune stimulation. TLR and STING agonists induced bone-marrow-derived myeloid cell cultures to secrete variable but notable levels of IL-1ra (Fig. 5a,b). In each case, IL-1ra induction was far greater than that seen for either IL-1α or IL-1β. Next, we injected a single systemic dose of lipopolysaccharide (LPS,TLR4 agonist), ODN1826 (TLR9 agonist), heat-killed Listeria monocytogenes (HKLM, a TLR2 agonist) or DMXAA (STING agonist) into wildtype or Il1rn−/− mice (Fig. 5c–f and Extended Data Fig. 8). As observed with RNA-LPX, increased sensitivity and self-limited hypothermia were observed in IL-1ra-deficient mice treated with these innate pro-inflammatory ligands (Fig. 5c,e and Extended Data Fig. 8a,c). Moreover, significant elevations in a range of serum cytokines were observed in Il1rn−/− mice (Fig. 5d,f and Extended Data Fig. 8b,d). These results indicate that high endogenous levels of IL-1ra can protect wildtype mice from immune dysregulation and uncontrolled systemic inflammation triggered by IL-1 for a range of innate stimulatory agents.
Lastly, T cell-based immunotherapies such as chimeric antigen receptor (CAR)T cells and tumor-directed/CD3-bispecific antibodies (TDBs) can also cause clinical CRS in human patients21,22,23,32. Instead of inducing a direct, primary release of IL-1β by innate stimuli (such as RNA-LPX), these immunotherapies have been shown to trigger a secondary induction of IL-1β, driven by activation of T cells21,22,23. We asked if IL-1β released secondary to initial stimuli would contribute to the development of CRS in Il1rn−/− mice bearing ID8 tumors expressing the surface antigen LyPD1. Following administration of an anti-LyPD1/CD3 TDB, upregulation of IL-1β expression in monocytes and macrophages was observed in vivo (Extended Data Fig. 9). The systemic release of IL-1β instigated a rapid decrease in core body temperature in TDB-treated Il1rn−/− mice (Fig. 5g), accompanied by elevated serum concentrations of IL-6 and IL-17A (Fig. 5h). Of note, the serum concentrations of TNF were comparable between genotypes (Fig. 5h). This further suggests that while T cells provide the initial trigger for CRS, T cell-derived TNF probably serves to activate monocytes and macrophages to release IL-1β, which was then directly responsible for the transient systemic response to TDBs in vivo. Importantly, these data suggest that induction of IL-6, which has been shown to be an important mediator of CRS toxicities related to T cell-targeting therapies21,22,23, can occur downstream of IL-1β.
Il1rn −/− mice adapt to excessive IL-1 via shedding of IL-1R1
Despite lacking the master negative regulator of IL-1, IL-1ra deficient mice should still possess the other presumed negative regulators of IL-1 activity. Indeed, increase in soluble IL-1R1 was observed in the serum of Il1rn−/− mice following stimulation with innate ligands (Fig. 6a), concomitant with reduction in cell-surface expression of IL-1R1 in vivo (Fig. 6b). This loss of membrane-bound IL-1R1 can decrease signaling and provide a soluble systemic IL-1α/β sink in the absence of IL-1ra. Interestingly, blockade of IL-1 signaling with a recombinant IL-1R1-Fc prevented the loss of cell-surface IL-1R1 in Il1rn−/− blood cells ex vivo (Fig. 6c), suggesting that the shedding of IL-1R1 only occurs following excessive IL-1 signaling (that is, in the absence of IL-1ra). In contrast to IL-1R1, the serum concentrations of decoy receptor IL-1R2 were only modestly increased over high baseline levels following stimulation (Fig. 6d), suggesting that shedding of IL-1R1 was the primary resistance mechanism by which Il1rn−/− mice adapt to excessive IL-1 signaling (Fig. 6e). However, these changes were secondary and only upregulated in the absence of IL-1ra, confirming that IL-1ra is the key suppressor of PRR-induced reactogenicity in wildtype mice.
Ionizable lipids in modRNA-LNP induce the release of IL-1
Our data with RNA-LPX indicated that both TLR7/8 agonistic function of the RNA and liposomes were required for production of IL-1, which mediated reactogenicity and immunogenicity of the vaccine. However, RNA vaccines against COVID-19 (mRNA-1273 by Moderna and BNT162b2 by BioNTech/Pfizer)—which use modRNA with a greatly reduced innate immunostimulatory activity—still elicit systemic adverse events in patients following initial intramuscular administration3,6,8,9. Instead of cationic liposomes, these vaccines are formulated in LNPs which contain ionizable lipids to provide structural stability and presumably enable endosomal escape7,33. While LNPs have been observed to have intrinsic adjuvant activity, demonstrated by the impressive antibody and T cell responses following vaccination3,6,8,9, the exact mechanism of by which such vaccines elicit innate immunity has not been previously characterized.
To test whether these particles could induce release of different IL-1 family members, we generated modRNA-LNPs formulated with two different ionizable lipids: MC3 (commonly used for short interfering RNA (siRNA)-LNP delivery33) or SM-102 (used in the Moderna COVID-19 vaccine8,33) (Fig. 7a). Consistent with our findings with RNA-LPX, we observed a marked increase in IL-1β from human PBMCs with either modRNA-LNP formulation, while the levels of IL-1α and IL-1ra remained low (Fig. 7b). LNPs formulated with SM-102 lipids were potent activators of the inflammasome pathway, indicated by the fact that robust IL-1β release was detected with either modRNA-LNP(SM-102) or empty LNP(SM-102) (Fig. 7c). Cotreatment with R848 and empty LNP(SM-102) further increased the IL-1β levels (Fig. 7c). In contrast, modRNA-LNP(MC3) was far less potent at stimulating IL-1β release, and even addition of a strong TLR7/8 agonist, R848, to LNP(MC3) could not fully rescue IL-1β release (Fig. 7c). These results suggest that ionizable lipids in different LNP formulations can play different, yet important, roles in inflammasome activation by providing either signal 2 (MC3) or signals 1 and 2 (SM-102).
To further study the relative contributions of RNA and lipids, we used modRNA to make RNA-LPX particles (modRNA-LPX) and compared their cytokine induction profile with RNA-LPX and modRNA-LNP(SM-102) (Fig. 7d). As shown previously (Fig. 1), unmodified RNA-LPX induced a robust cytokine release, whereas modRNA-LPX failed to induce IL-1β or any of its downstream cytokines (Fig. 7e). In contrast, potent cytokine release was detected with modRNA-LNP(SM-102), resulting in a similar cytokine induction profile as with RNA-LPX (Fig. 7e). These findings suggest that the reactogenicity of modified RNA is context-dependent: modRNA can be nonimmunostimulatory when formulated in liposomes (LPX), induce weak immunostimulation when formulated in LNP(MC3) or initiate a potent innate response when formulated in LNP(SM-102).
The evolution of the innate immune system for any species has in large part been shaped by microbe-exerted selection pressure for that species. While this has led to differences in distribution, sensitivity and ligand specificity of PRRs, it has also resulted in diverging evolutionary strategies for resistance and tolerance between humans and mice34. Relative to human immune responses, mice have been found to be extremely tolerant to different inflammatory stimuli13,14,34, such as bacterial lipopolysaccharides, but also RNA-LPX vaccines1,12. In this study, we demonstrated that vaccine-induced systemic inflammatory responses are driven by IL-1 and antagonized by endogenous IL-1ra, and that these findings can be generalized to other forms of innate immune stimulation. Interestingly, clinical use of recombinant IL-1ra (anakinra) may be effective for the treatment of auto-immune-related macrophage activation syndrome and severe forms of COVID-19, suggesting that IL-1R1 signaling can contribute to the early cytokine amplification following infection35,36,37. In line with these reports, we observed that administration of a virus-like nanoparticulate vaccine, RNA-LPX, leads to a robust upregulation of IL-1ra in wildtype B6 mice and confers resistance to adverse events, while Il1rn-/– mice exhibited a phenotype reminiscent of human CRS following innate immune challenge. These results suggest that endogenous IL-1ra has a crucial role in controlling innate immune responses to pathogens, as shown for Mycobacterium tuberculosis38. In addition, reduced sensitivity of mouse blood cells to RNA-LPX could be partially explained by the lower frequency of monocytes in mice when compared with humans, as we and others have identified monocytes as the crucial cell population secreting IL-1β and IL-6 following stimulation21,23. Accordingly, the absence of granulocytes in these cellular assays did not produce any changes in IL-1β release. Our studies with NHP PBMCs also suggest that NHPs resemble mice more than humans with respect to their monocyte frequencies and IL-1ra induction profile. Of note, NHPs and humans exhibit notable evolutionary differences in response to innate stimuli, and TLR7/8 agonists have been reported to be poor inducers of pro-IL-1β in NHP cells39.
Furthermore, our studies revealed that not only the direct TLR7/8-mediated sensing of the nucleic acid component, but also the physiochemical and possibly lytic properties of the vaccine lipid particles themselves, determine the cytokine induction profile of lipid-formulated RNA vaccines. Our data indicate that the immunostimulatory activity of the modRNA is highly dependent on the lipid formulation; modRNA formulated in LPX is nonimmunostimulatory and has been shown to induce tolerance40, while formulation in LNP(SM-102) leads to potent innate response, consistent with the reactogenicity and immunogenicity observed in mRNA-1273-vaccinated individuals8. Although modRNA poorly activates TLR7/8, it can have residual innate agonist properties, possibly resulting from double-stranded RNA contamination produced during in vitro transcription, remaining uncapped messenger RNA or mRNA tertiary structures, any of which can be a source of signal 1 by activating various endosomal (TLR3) and cytosolic receptors (for example, RIG-I, MDA-5). However, we also observed that empty LNP(SM-102) particles without RNA were sufficient for IL-1β release in vitro, suggesting that the lipids alone can provide both signals 1 and 2 for inflammasome activation. While we did not investigate the source of signal 1 in this context, it could be derived from direct activation of PRRs by the lipids themselves41,42,43, from the release of damage-associated molecular patterns following cell damage caused by LNPs44 or from the direct activation of caspase-11 (ref. 45). Future work will determine how these factors will influence the overall immunogenicity profile of LNP-based particles and whether such responses could be altered by the use of alternative lipid structures. Importantly, such optimizations will be crucial for the entire field of oligonucleotide therapeutics, where—unlike for adjuvanted vaccines—the induction of the innate immune cascade mediated by IL-1β would be undesirable (for example, LNP-based therapeutics delivering siRNA, antisense oligonucleotides or immune-tolerance-inducing mRNA).
In summary, our findings indicate that that IL-1ra-deficient mice can better predict patient responses to innate immune challenges (such as RNA vaccines) and provide a useful tool to evaluate both the sensitivity to pathogens and tolerability to treatment-related inflammatory toxicities in vivo. Moreover, the observed interspecies differences suggest that evolution has shaped and re-wired how positive and negative regulators of IL-1R1 signaling are released in the context of innate immune stimulation, and that these factors determine the magnitude of systemic responses to RNA vaccines in mice, NHPs and humans.
C57BL/6J mice (stock 000664) and Il1rn−/− mice (B6.129S-Il1rntm1Dih/J, stock 004754) were purchased from The Jackson Laboratory. Il1r1−/− mice were obtained from The Jackson Laboratory (B6.129S7-Il1r1tm1Imx/J, stock 003245) and backcrossed for eight generations to C57BL/6N mice (The Jackson Laboratory). Nlrp3−/− mice (also known as Cias1−/− mice) and Gsdmd−/− mice have been described15,46. Age-matched (5–15 weeks) female animals were used throughout all experiments. Mice were maintained in a specific-pathogen-free facility, in individually ventilated cages within animal rooms maintained on a 14-h/10-h, light/dark cycle. Animal rooms were temperature- and humidity-controlled, at 68–79 °F and 30–70%, respectively, with 10 to 15 room air exchanges per hour. All animal studies were reviewed and approved by Genentech’s Institutional Animal Care and Use Committee.
Depletion, inhibition and blocking experiments
Buffy coats or whole blood were obtained from voluntary, healthy human donors participating in the Genentech blood donor program, after written, informed consent from the Western Institutional Review board. As anonymous donors were used, covariate-relevant participant characteristics such as age and sex were not available. PBMCs were isolated by density centrifugation using SepMate-50 tubes and Lymphoprep Medium (both from StemCell Technologies). Red blood cells were lysed with ACK lysis buffer (Gibco) and remaining blood cells were passed twice through a 70-µm filter. Monocytes or neutrophils were depleted from either PBMCs or whole blood with anti-human CD14 MicroBeads (130-050-201, Miltenyi Biotec), EasySep Human CD14 Positive Selection Kit II (17858, StemCell Technologies) or EasySep HLA Chimerism Whole Blood CD66b Positive Selection Kit (17882, StemCell Technologies), respectively. NHP PBMCs were ordered frozen (from iQ Biosciences), thawed and rested overnight before RNA-LPX treatment.
First, 1.5–3.5 × 105 cells were plated on 96-U-well plates and stimulated with 1 μg ml−1 LPS-EK (InvivoGen), 10 μg ml−1 Nigericin (InvivoGen) or RNA-LPX with or without 0.1–5 μM MCC950 (Sigma), 1–50 μM Necrosulfonamide (Sigma-Aldrich), 1–30 μM zVAD-FMK (Promega), 0.5 μg ml−1 R848 (InvivoGen), 1–50 μM DPI (Calbiochem), 1–50 μM BAPTA-AM (Sigma-Aldrich), 1–100 μg ml−1 anti-IL-1β neutralizing antibodies (InvivoGen) or 1–100 μg ml−1 control IgG1 antibodies (InvivoGen). Of note, as R848, LPS or RNA-LPX were not washed away between priming (signal 1) and triggering (signal 2) to account for possible activation of alternative NLRP3 inflammasome47. After 17 h, the cells were pelleted down, and the supernatants were collected and stored at −80 °C until analysis.
RNA-LPX, modRNA-LNP, TLR agonists and immune challenge
RNAs were synthesized by Genentech. RNAs encoding for either MC38-derived neoantigens or eGFP have been described1,12. RNA was formulated with liposomes consisting of DOTMA and DOPE at a charge ratio (+):(−) of 1.3:2, yielding negatively charged RNA-LPX1. For some in vitro experiments using RNA-LPX, RNA was synthesized using pseudouridine instead of uridine and 5-methyl-cytosine instead of cytosine to reduce TLR activation10.
For in vitro experiments using modRNA-LNP, RNA was synthesized using 1-methyl-pseudouridine instead of uridine3, capping was performed cotranscriptionally using a trinucleotide cap 1 analog (CleanCap AG (3ʹ OMe) m7(3ʹOMeG)(5’)ppp(5ʹ)(2ʹOMeA)pG, Trilink)3 and RNA was purified with cellulose treatment48. Finally, modRNA-LNP was formulated with a lipid mixture consisting of an ionizable lipid (either Dlin-MC3-DMA or SM-102), distearoylphosphatidylcholine (DSPC), cholesterol and PEG-lipid (at molar ratios of 50:20:28:2 for the MC3 formulation or 50:10:38.5:1.5 for the SM-102 formulation) using a microfluidic mixer, as previously described49.
For in vivo experiments, RNA-LPX (dose indicated in respective figure legends), 10 μg of ODN1826 VacciGrade (InvivoGen), 1 μg of LPS-EB VacciGrade (InvivoGen) or 1 × 108 HKLM (InvivoGen) was injected intravenously or 300 μg of DMXAA (InvivoGen), 30 μg of mFlt3L (Genentech), 500 μg of rat IgG2a isotype (BioXCell) or 500 μg of anti-Ly6G antibodies (BioXCell) was injected intraperitoneally into C57BL/6 mice as described in the respective figures. At 4–6 h after immune challenge, mice were bled for cytokine analysis. Rectal body temperature and body weight were measured for a total of 6 d following exposure or until the values reached pretreatment levels.
TDB experiments in tumor-bearing mice
Generation and verification of ID8/LyPD1 cells has been described50. Briefly, ID8/LyPD1 is a murine ID8 ovarian cancer cell line expressing the tumor-associated antigen LY6/PLAUR Domain-containing 1 gene (LyPD1), which was generated by lentiviral transduction. Cells were passaged twice in vivo for faster growth kinetics before generating master and working cell banks, of which third and fourth passages were used for tumor experiments. Then, 4 × 106 ID8/LyPD1 tumor cells in Hank’s Balanced Salt Solution and Matrigel were inoculated subcutaneously in the 2/3 mammary fat pad of wildtype and Il1rn−/− mice. Tumor sizes were measured unblinded with a caliper twice a week and tumor volumes were calculated by using the equation (a2 × b)/2 (a, width; b, length). T cell retargeting to LyPD1 was achieved by administration of mouse CD3-bispecific TDB antibodies21,50. Once tumors reached the target volume of 100–300 mm3 (median 150 mm3, approximately 3–4 weeks after implantation), animals were randomly divided into treatment groups and injected intravenously with 10 mg kg−1 anti-LyPD1/anti-CD3 TDB antibodies (diluted in 20 mM histidine acetate pH 5.5, 240 mM sucrose, 0.02% Tween-20) or vehicle only. Animals were euthanized 24 h after TDB administration for flow cytometric analysis or when exhibiting signs of impaired health.
Blood and tissue preparation
Cardiac puncture under deep terminal anesthesia was used to collect a large volume of whole blood for downstream in vitro assays. Whole blood was stored in EDTA polypropylene tubes (Sarstedt) and red blood cells were lysed with ACK lysis buffer (Gibco). Retro-orbital bleeding under isoflurane anesthesia was used to collect peripheral blood samples. Blood was stored in gel-separator polypropylene tubes (Sarstedt) and incubated for 15 min at room temperature, after which the coagulated blood samples were centrifugated at 2,300g for 5 min. Clear serum was transferred to new tubes and stored at −80 °C for downstream assays.
Spleens were collected in cold PBS and single-cell suspensions were generated by mashing the spleen tissue through a 70-μm cell strainer (BD Falcon) in Hank’s-based Cell Dissociation Buffer (Gibco) supplemented with Liberase (Roche) and DNase I (ThermoFisher). Red blood cells were lysed with ACK lysis buffer (Gibco).
Single-cell suspensions were incubated in FACS buffer (PBS supplemented with 0.5% BSA and 0.05% sodium azide) containing anti-mouse CD16/CD32 (Mouse Fc Block, BD) or Human TruStain FcX (Human Fc Block, Biolegend) for 10 min before and during staining with the indicated antibodies. Staining reagents for murine cells included FITC anti-CD169 (3D6.112, Biolegend), PE anti-IL-1α (ALF-161, eBioscience), PerCP-Cy5.5 anti-CD3 (17A2, Biolegend), BUV395 anti-B220 (RA3-6B2, BD), PE anti-NK1.1 (PK136, Biolegend), BV510 anti-CD11c (N418, Biolegend), BUV737 anti-CD4 (GK1.5, BD), VioBlue anti-CD11b (M1/18.104.22.168, Miltenyi Biotec), APC anti-CD115 (AFS98, Biolegend), FITC anti-CD11b (M1/70, Biolegend), PeCy7 anti-pro-IL-1β (NJTEN3, eBioscience), BV711 anti-F4/80 (BM8, Biolegend), AF700 anti-Ly-6C (HK1.4, Biolegend), AF647 anti-Siglec-F (E50-2440, BD), BV785 anti-Ly-6G (1A8, Biolegend), APC anti-CD209b (22D1, eBioscience), FITC PD-1 (29F.1A12, Biolegend), AF700 CD8 (KT15, BioRad), V500 CD90.1 (53-2.1 Biolegend), APC-Cy CD4 (GK1.5, BD Biosciences), APC-H7 CD19 (1D3, BD Biosciences), BUV395 KLRG1 (2F1, BD Biosciences), PerCP-eFluor710 CD127 (SB/199, Invitrogen), PE TCF1/TCF7 (C63D9, Cell Signaling Technology), AF488 IFNg (XMG1.2, Biolegend), BUV395 TCRb (H57-597, BD Biosciences), PeCy7 CD8 (53-6.7, BD Biosciences), BV510 B220 (RA3-6B2, Biolegend), BV421 TNF (MP6-XT22, Biolegend), BV785 CD4 (RM4-5, Biolegend), APC CD107a (1D4B, Biolegend), PE IL-1R1 (JAMA-147, Biolegend) and BV421 IL-1R2 (4E2, BD Biosciences). Intracellular Fixation & Permeabilization Buffer Set (88-8824-00, eBioscience) was used for intracellular staining of cytokines. Foxp3/Transcription Factor Staining Buffer Set (00-5523-00, eBioscience) was used for intranuclear staining of TCF1. Mitochondrial ROS levels in human monocytes were measured using MitoSOX Red Mitochondrial Superoxide Indicator (Invitrogen). To assess purity of CD14- or CD66b-depleted human cell populations, PerCP-Vio700 anti-CD14 (TÜK4, Miltenyi Biotec), PE anti-CD66b (G10F5, Biolegend), PeCy7 anti-CD3 (SK7, BD), APC-H7 anti-CD19 (SJ25C1 BD) and V500 anti-HLA-DR (G46-6, BD) were used. To study human and NHP monocyte frequencies, cross-species reactive APC anti-CD14 (M5E2, Biolegend) was used. Cells were stained on ice for extracellular markers for 20–30 min followed by staining for intracellular markers for 60 min, and filtered using 30–40-μm filter plates (PALL). Samples were acquired with BD FACSDiva software v.8.0 on a BD FACSymphony (BD) and analyzed with Flow Jo v.10.7.1 (TreeStar). Dead cells and cell aggregates were excluded from analyses by Fixable Viability Dye eFluor 780 (eBioscience), LIVE/DEAD Fixable Near-IR (Dead Cell Stain Kit for 633- or 635-nm excitation, Invitrogen) or LIVE/DEAD Fixable Blue (Dead Cell Stain Kit for UV excitation, Invitrogen) staining and forward scatter area (FSC-A)/forward scatter height (FSC-H) characteristics.
Murine bone-marrow-derived cultures
Bone marrow cells collected from wildtype or Il1r1−/− mice were differentiated in RPMI with 10% heat-inactivated fetal bovine serum (Gibco), 1% Glutamax (Gibco), 2-mercaptoethanol (55 μM, Gibco), 100 ng ml−1 recombinant mFlt3L (Peprotech) and 10 ng ml−1 mGMCSF (Peprotech) for 13 d. Differentiated, immature cells were then plated at 300,000 cells per well on a 96-U-well plate and stimulated for 16 h with 5 μg ml−1 RNA-LPX (Genentech) or 0.1 μg ml−1 Pam3CSK4, 0.1 μg ml−1 FSL1, 108 bacteria per ml HKLM, 10 μg ml−1 poly I:C, 0.05 μg ml−1 LPS-EK, 0.1 μg ml−1 FLA-ST, 0.1 μg ml−1 ssRNA40/Lyovec, 0.1 μg ml−1 CL097, 0.1 μg ml−1 R848, 0.1 μg ml−1 R837, 5 μM ODN1585, 5 μM ODN1826, 5 μM ODN2395, 10 μg ml−1 c-di-AMP, 10 μg ml−1 DMXAA or 10 μg ml−1 2ʹ3ʹ-c-di-AM(PS)2 (Rp,Rp) (all from InvivoGen). After stimulation, the cells were pelleted down, and the supernatants were collected and stored at −80 °C until analysis.
Serum concentrations of murine cytokines were determined using a bead-based, Cytokine & Chemokine Convenience 26-Plex Mouse ProcartaPlex multiplex immunoassay supplemented with murine IFNα ProcartaPlex (ThermoFisher Scientific) according to the manufacturer’s instructions. Serum concentrations of soluble receptors were determined using MILLIPLEX MAP Mouse Soluble Cytokine Receptor Magnetic Bead Panel (Millipore). Acute phase proteins were determined using MILLIPLEX MAP Mouse Acute Phase Magnetic Bead Panel 2 (Millipore). ELISA was used for the detection of mIL-1α (R&D Systems), mIL-1ra (Abcam) and mSAA3 (Sigma-Aldrich).
For the detection of human cytokines in vitro, MILLIPLEX MAP Human Cytokine/Chemokine Magnetic Bead Panel Premixed 30-plex assay (Millipore) was used according to the manufacturer’s instructions. For the detection of human cytokines in vivo, Simoa assay (Quanterix) and DiscoveryMAP Multiplexes (Myriad RBM) were used according to the manufacturer’s instructions. For the detection of NHP cytokines in vitro, MILLIPLEX MAP Non-Human Primate Cytokine Magnetic Bead Panel Premixed 23-plex assay (Millipore) was used according to the manufacturer’s instructions. Values below the lower limit of quantification were set to zero. Luminex data were collected on Flex-Map 3D v.3.2 (Luminex Corporation) and analyzed with Bio-Plex Manager 6.1.1 and Microsoft Excel v.16.16.27.
Clinical trial design and samples
A first-in-human phase 1b study of RO7198457 (Autogene cevumeran), a systemically administered RNA-LPX, in combination with the anti-PD-L1 antibody atezolizumab was conducted in patients with locally advanced or metastatic solid tumors4,5 (ClinicalTrials.gov identifier NCT03289962). Briefly, RO7198457 was GMP-manufactured on a per-patient basis and contained up to 20 tumor-specific neoepitopes. The study protocols were approved by the relevant authorities and ethics committee. The study was conducted in accordance with all applicable laws and regulations, and in agreement with the International Council on Harmonisation of Good Clinical Practice (ICH-GCP) guidelines and the Declaration of Helsinki. Written, informed consent was obtained from all patients before enrollment. RO7198457 was administered intravenously at a dose of 25 μg and atezolizumab at a dose of 1,200 mg. Blood samples were obtained before vaccination (predose), and at 4–6 h and 24 h after RO7198457 administration. Plasma cytokines were measured from nine patients as shown in Figs. 1i and 3d (sample selection was based on plasma availability and existing ELISPOT data, while excluding patients that had received steroids at the time of vaccination).
Statistical analyses and data presentation
Statistical analyses and graphing were performed using GraphPad Prism v.9.1.0 for Mac OS. Illustrations were created with BioRender.com. All results are expressed as mean ± s.e.m. or median without interquartile range as indicated. Unpaired two-tailed Student’s t-test was used for comparison of two groups. One-way analysis of variance (ANOVA) was performed when more than two groups were compared, and multiple comparisons were corrected using Dunnett’s post hoc test or Sidak’s post hoc test. Two-way ANOVA was performed when both time and genotype or treatment were compared, and multiple comparisons were corrected using Dunnett’s post hoc test or Sidak’s post hoc test. *P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001 and ****P ≤ 0.0001. No statistical methods were used to predetermine sample size for animal experiments.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
The data that support the findings of this study are available from the corresponding author upon reasonable request.
No custom code or specific mathematical algorithms were used in this study.
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We thank N. Kayagaki, S. Schock, B. Lee, T. Junttila, I. Balter, K. Nutsch, A.-H. Herzner, J. Hagar, S. Cullen, R. Barreira da Silva, C. Carbone, A. Ritter, K. Banta, A. Chitre Elgin, A. Castiglioni, V. Romeo, V. Leveque, R. Sabado, B. Lauffer, V. Sunkari and the FACS laboratory and the Luminex core for technical advice and support; C. Cox, K. Newton, G. Strasser, B. Grellman, D. Montoya, T. Scholl and S. Powell for assistance with breeding and acquisition of animals; I. Rhee for comments; and the GO39733 study team for support in accessing and interpreting clinical data.
All authors except U.S. are current or former employees of Genentech (South San Francisco, USA). U.S. is a management board member and an employee at BioNTech AG (Mainz, Germany), and inventor on patents and patent applications related to RNA vaccines used in this study. U.S. has securities from BioNTech AG.
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a, b, RNA-LPX-induced cytokines secreted by human PBMCs (n = 3) following depletion of CD14 + monocytes or CD66b + neutrophils in vitro. The data are representative of two independent experiments with biologically independent samples. Data presented as median.
Extended Data Fig. 2 Intravenous administration of RNA-LPX induces secretion of both IL-1β and IL-1α in C57BL/6 mice.
a-g, IL-1β and IL-1α measured 6 hours after IV injection of RNA-LPX in serum (b, n = 9) and in splenic myeloid cell subsets (n = 7) (c, d, e, f, g). The data are pooled from two independent experiments with biologically independent samples (b-f). Significance was determined by using unpaired two-tailed Student’s t-test (b) or one-way ANOVA and Tukey’s multiple comparisons test (d, f). Data presented as mean ± SEM (g), otherwise median. Rpϕ, red pulp macrophage; MMϕ, marginal metallophilic macrophage; MZϕ, marginal zone macrophage.
a, Secretion of IL-1β, IL-6 and TNF from human PBCMs (n = 3) following treatment with RNA-LPX and either isotype antibodies or neutralizing antibodies against IL-1β, IL-6 or TNF. b, c, Secretion of cytokines from DC/macrophage cultures derived from bone-marrow of wildtype or IL-1R1 knockout mice (n = 3) following treatment with RNA-LPX in vitro. The data are representative of two independent experiments with biologically independent samples. Significance was determined using one-way ANOVA and Sidak’s multiple comparisons test. Data presented as mean ± SEM (a) or median (c).
Extended Data Fig. 4 Loss of NLRP3 inflammasome or gasdermin D does not affect RNA-LPX-induced cytokine release in C57BL/6 mice.
a, b, Serum cytokine levels in wildtype and NLRP3 deficient (Nlrp3-/-) mice (n = 7) after IV injection of RNA-LPX. c, d, Serum cytokine levels in wildtype and gasdermin D deficient (Gsdmd-/-) mice (n = 7) after IV injection of RNA-LPX The data are representative of two independent experiments with biologically independent samples. Significance was determined by using one-way ANOVA and Dunnett’s multiple comparisons test (b, d). Data presented as median.
a, b, Fold induction of RNA-LPX-induced cytokines over baseline levels in red blood cell depleted peripheral blood cells derived either from healthy human donors (n = 6) or from naive mice (n = 3 pooled samples). c, Levels of serum IL-1α, IL-1β and IL-1ra 6 hr post-RNA-LPX in C57BL/6 mice (n = 15) and Balb/c mice (n = 18) ordered from different vendors. d, RNA-LPX-induced cytokine secretion assay using non-human primate (NHP) PBMCs. e, Secretion of IL-1β and IL-1ra from NHP PBMCs following treatment with RNA-LPX. f, Frequency of CD14 + monocytes in representative samples of human, cynomolgus macaque and rhesus macaque PBMCs. The data are representative of two independent experiments (b, e, f) or pooled data from three independent experiments (c) with biologically independent samples. Data presented as median (c), otherwise mean ± SEM.
a, b, c, Blood cell composition (a, b), cell counts (c) and serum cytokines (d) in naïve wildtype (n = 10) and Il1rn-/- mice (n = 10). The data are pooled from two independent experiments with biologically independent samples. Significance was determined using one-way ANOVA and Sidak’s multiple comparisons test (c) or unpaired two-tailed Student’s t-test (d). Data presented as median.
Extended Data Fig. 7 Impact of myeloid cells on RNA-LPX induced systemic cytokine responses in vivo.
a, b, Systemic cytokine response in Ly6G-depleted wildtype (n = 8) and Il1rn-/- mice (n = 7) following RNA-LPX administration in vivo. e, Expression of decoy receptor IL-1R2 on splenic neutrophils 24 hr post-RNA-LPX (n = 7). f, g, Systemic cytokine response in Flt3L-pretreated wildtype (n = 6) and Il1rn-/- mice (n = 6) following RNA-LPX administration in vivo. The data are representative of two independent experiments with biologically independent samples. Significance was determined by using one-way ANOVA and Tukey’s multiple comparisons test (b, e) or by unpaired two-tailed Student’s t-test (c). Data presented as median.
Core body temperature (a, c) and serum proteins (b, d) in wildtype (n = 7) and Il1rn-/- mice (n = 7) after systemic administration of HKLM or ODN1826. Significance was determined using two-way repeated measures ANOVA and Sidak’s multiple comparisons test (a, c) or one-way ANOVA and Dunnett’s multiple comparisons test (b, d). Data presented as median (b, d), otherwise mean ± SEM.
a, b, Gating strategy (a) and expression of pro-IL-1β (b) in spleen cell subsets following vehicle (n = 8) or TDB administration (n = 10) in ID8/LyPD1 tumor-bearing mice. The data are pooled from two independent experiments with biologically independent samples. Significance was determined using unpaired two-tailed Student’s t-test. Horizontal bars indicate median.
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Tahtinen, S., Tong, AJ., Himmels, P. et al. IL-1 and IL-1ra are key regulators of the inflammatory response to RNA vaccines. Nat Immunol 23, 532–542 (2022). https://doi.org/10.1038/s41590-022-01160-y
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