bioRxiv Science⌕ Search

bioRxiv · 10.1101/2025.10.09.681501

Pam3CSK4 as a Cross-Species Adjuvant for Polysaccharide Vaccines: Efficacy in Humanized Mouse and Non-Human Primate Models

Abstract

Polysaccharide-based vaccines are critical for preventing bacterial infections, yet their efficacy is often limited by weak antibody responses. Unfortunately, efficacious adjuvants for licensed native polysaccharide vaccines are lacking. The TLR4 agonist, monophosphoryl lipid A (MPL), significantly increases antibody responses to capsular polysaccharides in mice via B cell-intrinsic TLR4 and MyD88-dependent signaling. However, due to the lack of TLR4-driven adjuvant effects on polysaccharide-specific responses in non-human primates and the limited responsiveness of human B cells to TLR4 agonists, we sought to identify alternative MyD88-activating TLR agonists that could serve as suitable adjuvants to enhance humoral responses to polysaccharide vaccines in humans. In vitro assays revealed the TLR1/2 agonist Pam3CSK4 synergized with strong BCR crosslinking to optimally enhance both mouse and human B cell activation and antibody secretion. In vivo, Pam3CSK4 alone had no effect, but when paired with a squalene-based emulsion significantly increased polysaccharide-specific antibodies in both immunocompetent and PBMC-humanized mice that proved highly protective against lethal pneumococcal infections. Although a dual TLR2-7 agonist showed similar potent in vitro activity, it failed to enhance polysaccharide-specific IgG responses in vivo, mirroring the antagonistic effects observed when TLR2 and TLR7 agonists were combined both in vitro and in vivo. By contrast, inclusion of Pam3CSK4 in an adjuvant containing MPL, synthetic cord factor, and squalene emulsion further augmented protective polysaccharide-specific antibody responses in mice and rescued adjuvant effects in non-human primates. These findings reveal Pam3CSK4-containing formulations as promising adjuvants for native polysaccharide vaccines, with strong translational potential to enhance humoral immunity in humans. One Sentence SummaryPam3CSK4-based adjuvants show promise for boosting protective antibody responses to polysaccharide vaccines.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Jennings-Gee, J. E., Adams-Sims, A. E., Haas, K. M.. 2025-10-11. Pam3CSK4 as a Cross-Species Adjuvant for Polysaccharide Vaccines: Efficacy in Humanized Mouse and Non-Human Primate Models. https://doi.org/10.1101/2025.10.09.681501

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Ksp37 is a rapidly mobilized NK cell secretory protein that engages FGF2

A key feature of natural killer (NK) cells is their preloaded arsenal of effector molecules, allowing them to rapidly respond upon activation. In this study, we characterized a previously unexplored secretory protein, termed killer-specific secretory protein of 37 kDa (Ksp37), which is highly abundant in differentiated CD56dim NK cells. Ksp37 is rapidly secreted in a dose-dependent and JAK-1 dependent manner upon low levels of cytokine stimulation, making it a sensitive readout for NK cell activation. Following secretion, intracellular levels were rapidly replenished, preserving responsiveness to subsequent cytokine stimulation. We found that Ksp37 is stored in polarized intracellular compartments distinct from those containing canonical cytotoxic effector molecules, including granzyme B and perforin, which require stronger stimulation for release. Lastly, we identified Ksp37 as a novel binding partner of fibroblast growth factor 2 (FGF2). This opens new avenues of exploration for the role of NK cells in remodeling their extracellular environment by modulating the FGF2-FGFR1 axis, which plays a key role in tumor growth, angiogenesis and tissue repair.

immunology↗

ACE-engineered human iPSC-derived neutrophils enhance host defense against multidrug-resistant bacterial infections

Severe neutropenia predisposes patients to life-threatening infections, while donor-dependent granulocyte transfusions are limited by availability and variable cell quality. Here, we engineered human induced pluripotent stem cells (iPSCs) to constitutively or inducibly express angiotensin-converting enzyme (ACE) and differentiated them into functional ACE-engineered neutrophils (ACE-iNeu). ACE expression enhanced granulocytic maturation, reactive oxygen species generation, inflammatory cytokine production, and antimicrobial signaling. ACE-iNeu exhibited enhanced bactericidal activity against methicillin-resistant Staphylococcus aureus and multidrug-resistant Pseudomonas aeruginosa. Following adoptive transfer into neutropenic mice, ACE-iNeu significantly reduced circulating and tissue bacterial burdens. Integrated metabolomic and transcriptomic analyses revealed ACE-associated alterations in adenine nucleotide abundance and developmental and inflammatory pathways. Together, these findings establish ACE engineering as a strategy to enhance the production and antimicrobial function of human iPSC-derived neutrophils and support further preclinical development of engineered granulocyte therapies for severe drug-resistant infections.

immunology↗

Tetravalent dengue mRNA vaccination orchestrates balanced four-serotype immunity with durable memory and protection in mice.

An effective dengue vaccine must establish durable immunity across four dengue virus (DENV) serotypes, evade antibody-dependent enhancement (ADE), and overcome immune imprinting from prior exposure. Here, we developed TetprM-E mRNA-LNP, a tetravalent vaccine comprising LNP-formulated nucleoside-modified mRNAs encoding DENV1-4 precursor membrane-envelope (prM-E) antigens, and evaluated its immunogenicity, durability, protection and breath across serotype-specific immune backgrounds. Three immunization strategies elicited neutralizing titers greater than 1:1500 against each serotype. Passive transfer of immune sera conferred 100% survival and reduced viremia after lethal DENV2 challenge in immunocompromised mice. Vaccination induced DENV envelope (env)-specific CD8+T cells and CD4-dependent germinal-center responses. DENV env-binding antibodies persisted for 34 weeks alongside DENV env-specific memory B cells. Vaccine-elicited sera showed no measurable in vitro ADE. Although monovalent priming initially biased antibody responses, TetprM-E mRNA-LNP vaccination broadened neutralization across DENV1-4 regardless of priming serotype. Together, TetprM-E mRNA-LNP elicits broad, durable, and protective immunity despite serologic constraints from pre-existing immunity.

immunology↗