Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

The dendritic cell identity crisis: why conflicting classifications demand a consensus framework?

Guilherme Souza-Silva1

  • 1University of São Paulo Brazil.

Immunology Letters
|June 29, 2026
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same journal

The malignancy within: what cancer teaches us about human bonds.

Immunology letters·2026
Same journal

Progranulin enhances complement component 5a-primed neutrophil activation in antineutrophil cytoplasmic antibody-associated vasculitis.

Immunology letters·2026
Same journal

The newly identified role of TRIM72, an E3 ligase, in NINJ1-mediated plasma membrane rupture: focus on its anti-inflammatory function.

Immunology letters·2026
Same journal

The subsets of circulating follicular helper T cells play an important role in the pathogenesis of Autoimmune thyroid diseases.

Immunology letters·2026
Same journal

Could bradykinin pathway inhibition change the course of severe hantavirus disease?

Immunology letters·2026
Same journal

Lactate-related diagnostic signature in rheumatoid arthritis: WGCNA and LASSO analysis with experimental validation.

Immunology letters·2026
See all related articles

Single-cell technologies reveal dendritic cell (DC) diversity but cause naming conflicts. A unified classification framework for DC subsets is needed for better disease understanding and therapies.

Area of Science:

  • Immunology
  • Cell Biology

Background:

  • Single-cell technologies offer high resolution of dendritic cell (DC) heterogeneity.
  • This has led to conceptual fragmentation and conflicting nomenclature in the field.
  • Divergent models of conventional type 2 DC (cDC2) ontogeny and the identity of the DC3 subset are debated.

Purpose of the Study:

  • To critically analyze conflicting classifications of DC subsets.
  • To focus on the cDC2A/DC2A developmental dichotomy and new populations like transitional DC-derived DC2s (tDC2s).
  • To emphasize the impact of these disputes on mechanistic understanding and therapeutic targeting.

Main Methods:

  • Critical analysis of existing literature and classifications.
  • Focus on ontogenetic and functional criteria for DC classification.

Related Experiment Videos

  • Integration of newly described DC populations.
  • Main Results:

    • Conflicting classifications of DC subsets, particularly cDC2s and DC3s, hinder scientific progress.
    • Distinct roles of pro-DC3s in viral myocarditis and tDC2s in immune tolerance highlight the importance of accurate classification.
    • Current disputes extend beyond semantics, impacting disease mechanisms and therapeutic strategies.

    Conclusions:

    • A consensus framework based on rigorous ontogenetic and functional criteria is urgently needed.
    • Harmonizing DC classification is crucial for translating high-resolution data into clinical insights.
    • Standardized nomenclature will advance mechanistic understanding and therapeutic targeting in immunology.