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

Structural differences between the two human complement C4 isotypes affect the humoral immune response.

O Finco1, S Li, M Cuccia

  • 1Department of Pathology Harvard Medical School, Boston, Massachusetts 02115.

The Journal of Experimental Medicine
|February 1, 1992
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 author

Consultation report - gonococcal immunoassays and standards for vaccine development.

Vaccine·2026
Same author

Biofabrication of an<i>in situ</i>hypoxia-delivery scaffold for cartilage regeneration.

Biofabrication·2025
Same author

Invasion of spontaneous germinal centers by naive B cells is rapid and persistent.

bioRxiv : the preprint server for biology·2023
Same author

The origin and stability of nanostructural hierarchy in crystalline solids.

Science advances·2018
Same author

Waterborne Norovirus outbreak at a seaside resort likely originating from municipal water distribution system failure.

Epidemiology and infection·2018
Same author

Human protective response induced by meningococcus B vaccine is mediated by the synergy of multiple bactericidal epitopes.

Scientific reports·2018
Same journal

Retraction: In vivo NCL targeting affects breast cancer aggressiveness through miRNA regulation.

The Journal of experimental medicine·2026
Same journal

Intravesical mesothelin-based CAR T cells targeting MUC16 effectively control bladder cancer in preclinical models.

The Journal of experimental medicine·2026
Same journal

Flawed translation triggers oncogenic B-T cell communication.

The Journal of experimental medicine·2026
Same journal

Correction: LCK'ed in: Inborn errors of immunity in LCK reveal how TCR signaling is calibrated.

The Journal of experimental medicine·2026
Same journal

Mechanobiology of inflammation: Pulling the strings of innate immunity.

The Journal of experimental medicine·2026
Same journal

Bile acid retention in efferocytic macrophages shapes their inflammatory status during cholangitis.

The Journal of experimental medicine·2026
See all related articles

Human complement C4A protein facilitates a secondary immune response, unlike C4B, in a guinea pig model. This highlights the biological significance of structural differences between C4A and C4B in adaptive immunity.

Area of Science:

  • Immunology
  • Complement System Biology
  • Protein Isotype Function

Background:

  • The human complement system comprises two major C4 isotypes, C4A and C4B, with known structural differences.
  • The biological relevance of these structural variations in immune function remains incompletely understood.
  • Complement component 4 (C4) plays a critical role in both innate and adaptive immunity.

Purpose of the Study:

  • To investigate the functional significance of structural differences between human C4A and C4B.
  • To determine if C4A or C4B is more critical for mounting an effective secondary immune response.

Main Methods:

  • Utilized a guinea pig model deficient in complement C4.
  • Transiently reconstituted C4-deficient guinea pigs with either human C4A or C4B protein.

Related Experiment Videos

  • Immunized the reconstituted animals with bacteriophage phi X174 to assess immune response.
  • Main Results:

    • Animals reconstituted with human C4A exhibited a secondary immune response, characterized by a switch from IgM to IgG antibodies.
    • Animals reconstituted with human C4B failed to demonstrate this secondary immune response.
    • This indicates a differential functional capacity between C4A and C4B in vivo.

    Conclusions:

    • Human C4A protein is biologically more important than C4B for initiating a robust secondary antibody response.
    • The structural differences between C4A and C4B directly impact their functional capabilities in the immune system.
    • This study provides crucial insights into the distinct roles of C4 isotypes in adaptive immunity.