# Klebsiella pneumoniae vaccines: Evolving the blueprint from traditional platforms to mucosal and nanoscale delivery

**Authors:** Jinping Hu, Yiyi Xie, Weiqi Guan, Linlin Huang, Xin Li

PMC · DOI: 10.1016/j.mtbio.2026.102919 · Materials Today Bio · 2026-02-13

## TL;DR

This review explores new vaccine strategies against Klebsiella pneumoniae, focusing on nanoscale and mucosal delivery to combat antibiotic-resistant strains.

## Contribution

The paper introduces nanovaccines and mucosal delivery as novel approaches for Klebsiella pneumoniae immunization.

## Key findings

- Nanovaccines like outer membrane vesicles and glycoconjugate nanoparticles show promise for KP immunization.
- Mucosal vaccination strategies may block infection at the site of colonization.
- Traditional and modern vaccine platforms are compared to guide future KP vaccine development.

## Abstract

Klebsiella pneumoniae (KP) is a critical global health threat due to carbapenem-resistant and hypervirulent strains, necessitating effective vaccines amid declining antibiotic efficacy. This review provides a timely and systematic analysis of the current KP vaccine landscape. We first outline the epidemiology of classical and hypervirulent KP (hvKP) and the corresponding protective host immunity, establishing a foundation for vaccination. A detailed survey of key antigenic targets, including polysaccharides and proteins, is presented. The core of this review critically assesses the spectrum of vaccine platforms, from traditional whole-cell and subunit vaccines to nanovaccine platforms. Distinctively, we place a dedicated focus on two transformative frontiers: nanovaccines—such as outer membrane vesicles (OMVs) and biosynthetic glycoconjugate nanoparticles—and mucosal vaccination strategies, emphasizing their unparalleled potential to block infection at the primary site of colonization. By synthesizing cutting-edge preclinical advances and addressing persistent translational challenges, this review serves as a timely and comprehensive resource, offering valuable insights to guide the future development of effective immunization strategies against this formidable pathogen.

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## Full-text entities

- **Genes:** Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Itga1 (integrin alpha 1) [NCBI Gene 109700] {aka CD49A, E130012M19Rik, Vla1}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Il4 (interleukin 4) [NCBI Gene 16189] {aka BSF-1, Il-4}, Tlr2 (toll-like receptor 2) [NCBI Gene 24088] {aka Ly105}, Cxcr5 (C-X-C motif chemokine receptor 5) [NCBI Gene 12145] {aka Blr1, CXC-R5, CXCR-5, Gpcr6, MDR15}, Omp (olfactory marker protein) [NCBI Gene 18378], Ptprc (protein tyrosine phosphatase receptor type C) [NCBI Gene 19264] {aka B220, CD45R, Cd45, L-CA, Ly-5, Lyt-4}, Ighv1-62 (immunoglobulin heavy variable 1-62) [NCBI Gene 668542] {aka IgG, IgM, IgVH, Igh}, trm (tremor) [NCBI Gene 22052], Il2 (interleukin 2) [NCBI Gene 16183] {aka Il-2}, Il17a (interleukin 17A) [NCBI Gene 16171] {aka Ctla-8, Ctla8, IL-17, IL-17A, Il17}, Cxcr6 (C-X-C motif chemokine receptor 6) [NCBI Gene 80901] {aka BONZO, STRL33}, Cd86 (CD86 antigen) [NCBI Gene 12524] {aka B7, B7-2, B7.2, B70, CLS1, Cd28l2}, Cps1 (carbamoyl-phosphate synthetase 1) [NCBI Gene 227231] {aka 4732433M03Rik, CPS, D1Ucla3}, Zmym2 (zinc finger, MYM-type 2) [NCBI Gene 76007] {aka 5830413P05Rik, FIM, MYM, RAMP, SCLL, Zfp198}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, Pomgnt2 (protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2) [NCBI Gene 215494] {aka Ago61, Gtdc2}, Il13 (interleukin 13) [NCBI Gene 16163] {aka Il-13}, Fas (Fas cell surface death receptor) [NCBI Gene 14102] {aka APO1, APT1, CD95, TNFR6, Tnfrsf6, lpr}, Ighg1 (immunoglobulin heavy constant gamma 1 (G1m marker)) [NCBI Gene 16017] {aka IgG1, Igh-4, VH7183}, Cd69 (CD69 antigen) [NCBI Gene 12515] {aka 5830438K24Rik, AIM, VEA}, Cd14 (CD14 antigen) [NCBI Gene 12475], Ighv1-9 (immunoglobulin heavy variable 1-9) [NCBI Gene 668478] {aka Gm16697, Igg2a}, Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}, gnd (generalized neuroaxonal dystrophy) [NCBI Gene 14698], Itgae (integrin alpha E, epithelial-associated) [NCBI Gene 16407] {aka A530055J10, CD103, aM290, alpha-E1, alpha-M290}
- **Diseases:** nosocomial infections (MESH:D003428), urinary tract infections (MESH:D014552), toxicity (MESH:D064420), endophthalmitis (MESH:D009877), bacteremia (MESH:D016470), infected (MESH:D007239), allergic reactions (MESH:D004342), tenderness (MESH:D063806), hepatic abnormalities (MESH:D056486), Bacterial (MESH:D001424), infectious (MESH:D003141), sepsis (MESH:D018805), colonization (MESH:D003108), OPS (MESH:C564877), MDR (MESH:D018088), pain (MESH:D010146), Inflammatory (MESH:D007249), liver abscess (MESH:D008100), trauma (MESH:D014947), necrotizing fasciitis (MESH:D019115), respiratory infection (MESH:D012141), asthma (MESH:D001249), AMR (MESH:D060467), CR-KP (MESH:D007710), pneumonia (MESH:D011014), bacterial pneumonia (MESH:D018410), autoimmune disorders (MESH:D001327), burn (MESH:D002056), mastitis (MESH:D008413), fever (MESH:D005334), acute (MESH:D000208)
- **Chemicals:** fosfomycin (MESH:D005578), salmochelin (MESH:C000630262), oligosaccharide (MESH:D009844), aerobactin (MESH:C031819), H&amp;E (MESH:D006371), A1102 (-), AS03 (MESH:C550253), CR (MESH:D002857), cephalosporins (MESH:D002511), lipid (MESH:D008055), LPS (MESH:D008070), imipenem (MESH:D015378), formaldehyde (MESH:D005557), beta-lactam (MESH:D047090), PLGA (MESH:D000077182), galactosamine (MESH:D005688), alginate (MESH:D000464), yersiniabactin (MESH:C104398), O (MESH:D010100), O-antigen (MESH:D019081), enterobactin (MESH:D004758), PA (MESH:D011478), mannose (MESH:D008358), LTA1 (MESH:C009900), Polysaccharide (MESH:D011134), cefiderocol (MESH:C000612166), tetracyclines (MESH:D013754), meropenem (MESH:D000077731), levofloxacin (MESH:D064704), iron (MESH:D007501), carbapenem (MESH:D015780), lipid A. (MESH:D008050), SDS (MESH:D012967)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rodentia (rodent, order) [taxon 9989], Haemophilus influenzae (species) [taxon 727], Bos taurus (bovine, species) [taxon 9913], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986], Escherichia coli (E. coli, species) [taxon 562], Candida albicans (species) [taxon 5476], Salmonella enterica subsp. enterica serovar Typhi (no rank) [taxon 90370], Klebsiella pneumoniae (species) [taxon 573], Mus musculus (house mouse, species) [taxon 10090], Macaca (macaque, genus) [taxon 9539], Lactobacillus acidophilus (species) [taxon 1579], Streptococcus pneumoniae (species) [taxon 1313], Streptococcus pyogenes (species) [taxon 1314], Ophiostoma sp. 1 (species) [taxon 2268574]
- **Cell lines:** pET-28a — Oryctolagus cuniculus (Rabbit), Transformed cell line (CVCL_6E94), AP205 — Homo sapiens (Human), Xeroderma pigmentosum variant type, Transformed cell line (CVCL_2556), /c — Mus musculus (Mouse), Hepatocellular carcinoma of the mouse, Cancer cell line (CVCL_9103)

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12927087/full.md

## References

170 references — full list in the complete paper: https://tomesphere.com/paper/PMC12927087/full.md

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Source: https://tomesphere.com/paper/PMC12927087