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Hermans, I. F.

Publications and source records attributed to Hermans, I. F..

7 recordsLinked to original sources

Optimization of a liver Trm cell-inducing mRNA vaccine by reduction of type I interferon response

CD8+ tissue-resident memory T cells provide rapid frontline protection at pathogen invasion sites, making them attractive targets for vaccine-mediated immunity. We previously developed an NKT cell-adjuvanted mRNA lipoplex vaccine capable of inducing liver Trm cells and sterile protection against malaria in mice. Here, we show that type I interferon (IFN-I) signalling through dendritic cells -- not T cells -- is a key brake on liver Trm induction by this vaccine. Optimising mRNA manufacturing to reduce immunostimulatory contaminants substantially dampened IFN-I production, boosted antigen expression in the lymphoid tissues, and drove significantly greater Trm accumulation. These enhanced responses translated into superior protection against parasite challenge. Our findings identify DC-intrinsic IFN-I signalling as a tractable target, and mRNA manufacturing quality as a critical and underappreciated lever, for maximising Trm-based vaccine efficacy.

immunology↗

Temporal expression of liver-stage malaria antigens shapes vaccine efficacy

Vaccine-induced cytotoxic T cells can prevent malaria by killing parasite-infected hepatocytes during the liver stage. While several antigenic targets have been identified, little consideration has been given to their temporal expression. Here, we identified SERA1 of Plasmodium berghei as a late liver-stage target in rodent malaria and further showed that the classic vaccine antigen thrombospondin-related adhesion protein (TRAP) is only an early target. While vaccination with either antigen alone was modestly protective, combining these antigens enabled killing over the entire liver-stage, greatly improving efficacy. Given the relatively long liver-stage in human malaria, our findings imply TRAP-dependent vaccines likely utilize only a small proportion of the available liver-stage to eradicate parasites. Our findings further indicate that considerations of temporal coverage when selecting vaccine antigens will improve efficacy. One-Sentence SummaryTemporally defining presentation of liver-stage antigens informs rational combinations that maximize malaria vaccine efficacy.

immunology↗

Engineering antigenic breadth against SARS-CoV-2 by pairing divergent RBDs within a single mRNA immunogen

Vaccines capable of eliciting broadly neutralising antibodies (bnAbs) are a major goal for pandemic preparedness. A persistent challenge across vaccine Wields is how to deliberately recruit the rare B cell clones that recognise conserved epitopes shared across diverse viral variants. BnAbs have been known to frequently emerge through extensive somatic hypermutation during afWinity maturation, here we describe an alternative, structure-driven mechanism for bnAb selection. We designed an mRNA vaccine in which two antigenically distinct SARS-CoV-2 variants (Omicron and Delta; O-{Delta}) receptor binding domains (RBDs) are physically fused on a single polypeptide. This design is predicted to favour B cell antigen receptors capable of engaging conserved epitopes on both RBDs with enhanced avidity. A matched non-divergent tandem RBD (Delta-Delta; {Delta}-{Delta}) served as a control. The divergent (O-{Delta}) immunogen was robustly expressed and retained high-afWinity ACE2 binding. In mice, immunisation elicited potent antibody responses and increased the frequency of antigen-speciWic cross-reactive B cells, recognising Delta, Omicron, and the 2002 pandemic strain SARS-CoV RBDs. Using multicolour RBD tetramers and single-cell B cell receptor sequencing, we show that breadth arises via two distinct pathways. The divergent vaccine preferentially enriches clonally distinct cross-reactive B cells (not present within non-cross-reactive B cell pools) with low levels of somatic hypermutation (SHM), consistent with selection of germline-biased precursors. In contrast, the matched control vaccine yields cross-reactivity primarily within existing clonal lineages (clonal overlap between cross-reactive and non-cross-reactive cells) and at higher mutational burdens, consistent with afWinity-maturation-driven acquisition of breadth. Together, these Windings demonstrate that antigen structure can bias B cell selection towards cross-reactive speciWicities without requiring extensive SHM. This work establishes a simple, modular antigen-design principle in which juxtaposing appropriately divergent antigens on a single scaffold promotes the enrichment of bnAb-prone B cells, providing a scalable strategy for vaccine development against rapidly evolving pathogens.

immunology↗

A new genetically engineered transplant model of glioma recapitulates key phenotypes of low- and high-grade gliomas

Immune competent animal models are essential in preclinical glioma research. The ability to investigate tumor development with key tumor microenvironment components such as immune infiltration, stromal cells and extracellular matrix allows for the investigation of these complex tumors. However, the current range of syngeneic models of glioma possess intrinsic limitations which must be acknowledged when designing a preclinical study. To address this gap, we developed genetically engineered mouse cell line models (GEM-CLeMs) by introducing common glioma driver mutations into immortalized astrocytes. A high-grade glioma model was generated by combining Pten knockdown with RAS V12 overexpression, while a low-grade glioma model was produced through p53 knockdown with mutant IDH1R132H overexpression. The RAS/Pten GEM-CLeM tumors grew rapidly in vivo, displayed necrosis, multinucleated pleomorphisms, abundant vascularization, and showed strong enrichment for extracellular matrix remodelling and mesenchymal genes, features closely aligned with human glioblastoma. Importantly, the RAS/Pten GEM-CLeM tumors showed similar survival trends and immune infiltration patterns as a corresponding KrasG12D/PtencKO GEMM, but could be grown to larger sizes, facilitating better stromal and immune analyses. In contrast, the IDH1R132H/p53 GEM-CLeM formed slow-growing tumors with distinctive immune infiltration and vascular patterns, consistent with low-grade glioma phenotypes. Compared with the commonly used cell line GL261, the GEM-CLeM tumors had higher levels of stromal integration and immune suppression, making them a more faithful model of the glioma tumor microenvironment. This system enables rapid generation of transplantable glioma models with defined driver mutations in a low-mutational background, offering a flexible platform for dissecting glioma biology and evaluating immunotherapies. Importance of the studyWe have generated a set of customizable, modular Genetically Engineered Mouse Cell Line Models (GEM-CLeMs) of "high grade" and "low grade" glioma. They reliably form tumors when transplanted intracranially into immune-competent C57BL/6 mice, and they are cost- and time-effective at capturing the important characteristics of glioma, both mutant IDH1 low grade glioma and high grade glioblastoma. Critically these characteristics include the myeloid-rich immune suppressive tumor immune microenvironment, a key weakness of existing murine glioma cell lines like GL261. These GEM-CLeM models can be used in multiple ways. The cells are amenable to further manipulation, so therapeutic targets and drug mechanism of action can be assessed. The activity of candidate genes in tumour formation and phenotype can be determined. Most importantly the models can be used to develop effective immunotherapies, including strategies to target macrophage and myeloid cell immune suppression. Key pointsO_LICombinations of driver mutations were engineered into an immortalised mouse astrocyte. C_LIO_LIEngineered cells formed tumours on intracranial transplant into immune competent mice. C_LIO_LITumors had key histological and immune suppressive features of human glioma. C_LI

cancer biology↗

Tarloxotinib targets tumor hypoxia to improve therapeutic efficacy of immune checkpoint inhibition in a TLR9 dependent manner

Immune checkpoint inhibitors can elicit deep and durable immune responses although most cancer patients fail to experience long-term remission. There is consensus that tumor hypoxia coordinates a multitude of underlying resistance mechanisms that contribute to treatment failure. Here we show that the clinical-stage hypoxia-activated prodrug tarloxotinib lowers tumor hypoxia 8-fold in the EGFR-dependent MB49 syngeneic tumor model, attracting a effector CD8+ T cell infiltrate into an oxygen enriched tumor microenvironment, leading to potentiation of checkpoint inhibitor activity. Various methodologies, including CD8+ T cell depletion and exogenous T cell priming confirmed that tarloxotinib has a positive impact on the function of activated CD8+ T cells. Whilst anti-PD-L1, anti-PD-1 and anti-CTLA-4 treatments all benefited from the remodeled tumor microenvironment, anti-PD-L1 was most responsive to tarloxotinib coadministration, providing a 100% complete response rate and >360% improvement in tumor growth delay (day 19; p<0.0001). This robust interaction was associated with MB49 tumor enrichment of CD8+ T cell infiltrate from 8% to 43% of the total CD45+ population. To further understand these promising observations, comparative RNA transcript analysis of 770 cancer/immune related genes in naive and tarloxotinib treated tumors highlighted the strong induction of gene clusters related to co-stimulatory signaling, cytokine/chemokine signaling, interferon signaling, immune cell adhesion/migration, antigen presentation and the lymphoid/myeloid compartments. Serum protein analysis confirmed upregulation of a mixture of cytokines/chemokines, including IL-6, IL-12p40, IFN{gamma}, G-CSF and MIP-1{beta}, amongst others. The source of this broad immunogenic response was identified as toll-like receptor 9 (TLR9) dependent, with the positive interaction between anti-PD-L1 and tarloxotinib blocked in MyD88 or TLR9 knockout mice. Further, the observed therapeutic interaction was still evident in MC38 and EG7.OVA syngeneic tumor models, both refractory to tarloxotinib by virtue of EGFR-signal independence. Consistent with the clinical experience of minimal systemic toxicities related to EGFR inhibition (e.g. diarrhea), mouse body weight loss was minimal across all in vivo studies and histopathology screening for evidence of lung fibrosis proved negative. Tarloxotinib therefore represents a systemically administered small molecule with an established clinical safety profile that is capable of activating TLR9 signaling within tumors whilst remodeling the microenvironment to facilitate efficacy of checkpoint blockade. What is already known on this topicSolid tumor resistance to immune checkpoint inhibitors (ICI) is orchestrated through a diverse collection of hypoxia-driven mechanisms. In preclinical models modifying the tumor microenvironment (TME) to lessen hypoxia typically improves responses to ICI. What this study addsTarloxotinib is a hypoxia-activated prodrug (HAP) of an irreversible EGFR/HER2 TKI that profoundly remodels the TME, both eliminating tumor hypoxia and elevating cytokine/chemokine production via a TLR9 dependent effect. Together, this results in a marked tumor influx of activated CD8+ T cells (and other TILs), that results in major improvements in the efficacy of ICIs, particularly anti-PD-L1. How this study might affect research, practice or policyTarloxotinib is the first example of a tumor-targeted small molecule TLR9 stimulant that restores ICI sensitivity in a range of syngeneic tumor models. Phase I/II data has demonstrated that tarloxotinib is well tolerated, with few EGFR-dependent (on-target) side-effects, reflecting minimization of normal tissue exposure with the tumor-targeted HAP approach. Importantly, it also optimizes tumor selective exposure, offering a compelling clinical rationale for evaluation of this combination in cancer patients experiencing ICI relapse or resistance.

immunology↗

MAIT cells activate dendritic cells to promote T follicular helper cell differentiation and humoral immunity

Protective immune responses against respiratory pathogens, including influenza virus are initiated by the mucosal immune system. However, most licensed vaccines are administered parenterally and are largely ineffective at inducing mucosal immunity. The development of safe and effective mucosal vaccines has largely been hampered by the lack of a suitable mucosal adjuvant. In this study we explore a novel class of adjuvant that harness mucosal-associated invariant T (MAIT) cells. We show evidence that intranasal immunisation of MAIT cell agonists co-administered with protein, including haemagglutinin from influenza A virus induced potent humoral immunity and immunoglobulin (Ig)A production, which protected mice against infection. MAIT cell adjuvant activity was mediated by CD40L-dependent activation of dendritic cells and subsequent priming of CD4+ T follicular helper cells. In summary, we show that MAIT cells are promising vaccine targets that can be utilised as cellular adjuvants in mucosal vaccines.

immunology↗

Single-cell analysis of intestinal immune cells during helminth infection

Single cell isolation from helminth infected intestines has been notoriously difficult, due to the strong anti-parasite type 2 immune responses that drive mucus production, tissue remodeling and immune cell infiltration. Through the systematic optimization of a standard intestinal digestion protocol, we were able to isolate millions of immune cells from heavily infected tissues. Using this protocol, we validated many hallmarks of anti-parasite immunity and analyzed immune cells from the lamina propria and granulomas during helminth development, as well as acute and chronic worm infection.

immunology↗