Evidence map›Paper›PMID 42812797›Full record

ReviewFrontiers in immunology2026

Mechanisms and applications of camelid variable heavy-chain nanobodies against bacterial and parasitic protozoal pathogens.

Hattan S Gattan, Thamir A Alandijany

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Hattan S Gattan *Special Infectious Agents Unit, King Fahd Medical Research Center, King Abdulaziz University, Jeddah, Saudi Arabia.
Thamir A Alandijany *Special Infectious Agents Unit, King Fahd Medical Research Center, King Abdulaziz University, Jeddah, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Camelid variable heavy-chain (VHH) nanobodies have emerged as a promising class of single-domain antibodies with significant potential for combating bacterial and parasitic infections. Their small molecular size, high solubility, exceptional physicochemical stability, and ability to recognize cryptic or conformational epitopes inaccessible to conventional antibodies enable unique therapeutic applications. This review summarizes recent advances in the biology, mechanisms of action, engineering, and translational potential of camelid VHH nanobodies against bacterial and parasitic pathogens. In bacterial infections, nanobodies primarily function as anti-virulence agents by neutralizing toxins, inhibiting bacterial adhesion and invasion, disrupting secretion systems, preventing biofilm formation, and targeting antimicrobial resistance determinants such as β-lactamases. In protozoal diseases, they exhibit diverse mechanisms including direct killing, inhibition of host-cell invasion, disruption of surface protein trafficking, interference with metabolic pathways, and blockade of transmission stages. We further discuss current approaches for nanobody generation, recombinant production, molecular engineering, and optimization, together with challenges related to pharmacokinetics, immunogenicity, manufacturing, and clinical translation. Finally, emerging applications involving artificial intelligence-assisted nanobody design, nanotechnology-based delivery systems, One Health strategies, and outbreak preparedness are highlighted. Collectively, camelid VHH nanobodies represent a versatile and highly engineerable platform with considerable potential to address antimicrobial resistance, and accelerate the development of next-generation antimicrobial therapeutics.

Indexed as

Bacterial InfectionsCamelidaeImmunoglobulin Heavy ChainsParasitic DiseasesSingle-Domain AntibodiesAnimalsCamelids, New WorldHumansImmunoglobulin Heavy ChainsSingle-Domain Antibodiesbacterial infectionscamelid nanobodiesimmunotherapyOne Healthparasitic infectionssingle-domain antibodiesVHH

Identifiers

PMID42812797
PMCPMC13620469

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.