Evidence map›Paper›PMID 41853324›Full record

ReviewThe World Allergy Organization journal2026

What is new on the horizon for the biologics world: New kids of the block - WAO state of art.

Giorgio Walter Canonica, José Antonio Ortega-Martell, Rosalaura V Villarreal-González, Ignacio J Ansotegui, Claus Bachert, Jonathan Bernstein, Eugene Bleecker, Benedetta Bondi, Marco Caminati, Tara Carr and 18 more

Abstract readReview
In one paragraph

Review in The World Allergy Organization journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

28 authors.

Giorgio Walter CanonicaHumanitas University and, IRCCS Humanitas Research Hospital, Milan, Italy.
José Antonio Ortega-MartellInstitute of Health Sciences, Autonomous University of the State of Hidalgo (UAEH), Pachuca, Hidalgo, Mexico.
Rosalaura V Villarreal-GonzálezOncology Service, Hospital Universitario "Dr. José Eleuterio González", Faculty of Medicine, Universidad Autónoma de Nuevo León, Monterrey, Mexico.
Ignacio J AnsoteguiHospital Quironsalúd Bizkaia, Erandio, Bilbao, Spain.
Claus BachertUniversity Hospital of Ghent, Ghent University, Ghent, Belgium.
Jonathan BernsteinUniversity of Cincinnati Medical Center, Cincinnati, OH, United States.
Eugene BleeckerMayo Clinic, Scottsdale, AZ, United States.
Benedetta BondiSan Martino Polyclinic Hospital, University of Genoa, Genoa, Italy.
Marco CaminatiUniversity of Verona, Verona, Italy.
Tara CarrDepartment of Medicine, University of Arizona, Phoenix, AZ, United States.
Antonella CianferoniChildren's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Ignacio Dávila GonzálezUniversity Hospital of Salamanca, Salamanca University, Salamanca, Spain.
Sandra González DíazHospital Universitario "Dr Jose Eleuterio Gonzalez", Universidad Autónoma de Nuevo León, Monterrery, Nuevo León, Mexico.
René Maximiliano GómezCatholic University of Salta, Salta, Argentina.
Nicola HananiaBen Taub Hospital, Baylor College of Medicine, Houston, TX, United States.
Enrico HefflerHumanitas Research Hospital, Humanitas University, Milan, Italy.
Parameswaran NairMcMaster University and, Firestone Institute for Respiratory Health, St. Joseph's Healthcare, Hamilton, Ontario, Canada.
Nida ÖztopMunich Technical University, Munich, Germany.
Hae-Sim ParkAjou University, Seoul, South Korea.
Helena PitèCUF Descobertas Hospital, Lisbon, Portugal.
Phillip RouadiDar Al Shifa Hospital, Hawally, Kuwait.
Hirohisa SaitoNational Center for Child Health and Development, Tokyo, Japan.
Massimo TriggianiUniversità degli Studi di Salerno, Salerno, Italy.
Gilda VarricchiUniversity of Naples Federico II, Naples, Italy.
Christian VirchowUniversity Hospital, University of Rostock, Rostock, Germany.
Yoshiyuki YamadaTokai University School of Medicine, Isehara, Kanagawa, Japan.
Anahí YáñezCenter for Research on Allergies and Respiratory Diseases (INAER), Buenos Aires, Argentina.
Mário Morais-AlmeidaCUF Descobertas Hospital, Lisbon, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Advances in the understanding of type 2 inflammation have driven the development of novel biologics and small molecules for allergic diseases. New therapies targeting cytokines, receptors, and intracellular pathways offer opportunities to refine disease management and modify long-term outcomes. Methods: The World Allergy Organization (WAO) Biologics Therapies in Allergic Diseases Committee conducted this state-of-the-art review. We analyzed current literature on investigational monoclonal antibodies, nanobody-based agents, kinase inhibitors, and small molecules with potential applications in asthma, chronic rhinosinusitis with nasal polyposis, atopic dermatitis, and chronic spontaneous urticaria. Mechanistic considerations, therapeutic targets, and clinical trial outcomes were evaluated to highlight emerging trends in biologic and small-molecule therapy. Results: Biologics targeting IL-4, IL-5, IL-13, IL-31, TSLP, and IgE continue to expand therapeutic options across allergic disorders. Innovations such as Fc-engineered antibodies, bispecific antibodies, and nanobody platforms enhance efficacy, extend half-life, and improve tissue penetration. Novel intracellular inhibitors, including JAK, SYK, and STAT6 degraders, show promise as oral alternatives to injectable therapies. Clinical trials report high efficacy and favorable safety profiles, though variability remains across diseases and endotypes. Pediatric data are limited, and the long-term safety and cost-effectiveness of this approach require further evaluation. Conclusions: Emerging biologics and small molecules are transforming the therapeutic landscape of allergic diseases, providing targeted and personalized interventions. Advances in molecular engineering, particularly nanobody technology and intracellular inhibitors, hold promise for improving patient outcomes and reducing treatment burden. Future research should prioritize long-term safety and standardized approaches to optimize integration of these therapies into clinical practice.

Indexed as

Allergic diseasesBiological productsInflammation type 2Janus kinase inhibitorsMonoclonal antibodies

Identifiers

PMID41853324
PMCPMC12992511

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.