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

Autoantibodies to complement components.

L A Trouw1, A Roos, M R Daha

  • 1Department of Nephrology, D3-P, Leiden University Medical Center, Albinusdreef 2, 2333 ZA Leiden, The Netherlands. trouw2@lumc.nl

Molecular Immunology
|September 5, 2001
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

Post-translationally modified proteins bind and activate complement with implications for cellular uptake and autoantibody formation.

Journal of autoimmunity·2025
Same author

Anti-myeloperoxidase IgM B cells in anti-neutrophil cytoplasmic antibody-associated vasculitis.

Nature communications·2025
Same author

The frequency of HLA-DQ7 in patients at risk of coeliac disease: A haplotype to be reckoned with for screening?

Human immunology·2024
Same author

Generation of two induced pluripotent stem cell lines (HIMRi006-A and HIMRi007-A) from Pompe patients with infantile and late disease onset.

Stem cell research·2024
Same author

Hippocampus, amygdala, and insula activation in response to romantic relationship dissolution stimuli: A case-case-control fMRI study on emerging adult students.

Journal of affective disorders·2024
Same author

Generation of two hiPSCs lines of two patients carrying truncating mutations in the dimerization domain of filamin C.

Stem cell research·2024
Same journal

m6A modification of LINC00458 enhances HMOX1 stability via ELAVL1 recruitment to promote ferroptosis and aggravate asthma.

Molecular immunology·2026
Same journal

Overexpression of Hes1 inhibits cigarette smoke-induced mitochondrial apoptosis in AT2 cells by activating the Pgc-1α/Tfam signaling pathway.

Molecular immunology·2026
Same journal

Progesterone promotes favorable pregnancy outcomes in recurrent spontaneous, abortion by attenuating NK Cell overactivation and upregulating the cAMP/PKA/CREB signaling axis.

Molecular immunology·2026
Same journal

Oleanolic acid alleviates hepatic fibrosis by inhibiting liver macrophage recruitment and polarization.

Molecular immunology·2026
Same journal

Cordycepin attenuates diabetic nephropathy by dual-pathway activation of TFEB to restore autophagy and ameliorate podocyte injury.

Molecular immunology·2026
Same journal

Endothelial-derived TWEAK drives granulosa cell apoptosis in PCOS via the Fn14-oxidative stress axis.

Molecular immunology·2026
See all related articles

Autoantibodies targeting the complement system, a key part of innate immunity, can cause host damage and secondary deficiencies. Their role in disease requires further investigation.

Area of Science:

  • Immunology
  • Innate Immunity

Background:

  • The complement system is crucial for innate immunity but can cause harm when dysregulated.
  • Autoantibodies against complement components, regulators, and receptors are known to exist.

Purpose of the Study:

  • To review autoantibodies targeting the complement system.
  • To discuss their effects on complement levels and host susceptibility to infections.

Main Methods:

  • Literature review of studies on complement autoantibodies.

Main Results:

  • Autoantibodies against complement components can lead to their depletion, causing secondary complement deficiency.
  • The presence of these autoantibodies is associated with disease but causal links are not always clear.

Related Experiment Videos

  • Pathology likely involves multiple contributing factors, not just autoantibodies alone.
  • Conclusions:

    • Autoantibodies against complement components can impair immune function and increase infection risk.
    • Further research is needed to fully understand the pathogenic mechanisms and clinical significance of complement autoantibodies.