Search results for "Complement components"

showing 6 items of 6 documents

Research on complement: old issues revisited and a novel sphere of influence

2003

Immunology in recent years has taken a somewhat surprising turn, expressed by a renewed interest in innate immunity. Especially intriguing is the regulatory role exerted by the innate components on the adaptive response, with Toll receptors and complement components being the most investigated. This function has been firmly established for complement protein CR2 (CD21) as part of the BCR co-receptor CD19/CD21/CD81. New findings are now providing a broader picture of complement and its tuning of the immune response; for example, complement proteins have been implicated in the control of T-cell-mediated responses. We will review some of these data here and summarize new discoveries in areas o…

Membrane GlycoproteinsInnate immune systemT-LymphocytesImmunologychemical and pharmacologic phenomenaComplement System ProteinsComplement C1 Inactivator ProteinsBiologyImmunity InnateComplement componentsComplement systemComplement (complexity)Membrane Cofactor ProteinImmune systemAntigens CDComplement Factor HImmunologyAnimalsHumansImmunology and AllergyKidney DiseasesSphere of influenceComplement C1 Inhibitor ProteinSerpinsTrends in Immunology
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Seminal plasma-induced suppression of the respiratory burst of polymorphonuclear leukocytes and monocytes.

1984

Summary: Based on recent findings indicating suppression of lymphocytic functions by seminal plasma (SP) we tested the effects of SP from men with normo- and oligozoospermia (n = 7, each) on the generation of luminol-enhanced chemiluminescence (CL) of polymorphonuclear leukocytes (PMN) and monocytes (Mo) stimulated in vitro with zymosan. We found a complete suppression of CL of PMN and Mo by undiluted SP's, 1,000-fold dilutions still induced ≥ 20 percent inhibition. There was no difference between normo- and oligozoospermic men in inhibition of CL both with PMN and Mo. Protein concentrations of SP's were closely the same; all SP were free of the complement components C4 and C3c. After dialy…

Malemedicine.medical_specialtyNeutrophilsUrologyPercent InhibitionMonocytesComplement componentschemistry.chemical_compoundEndocrinologyOxygen ConsumptionSemenInternal medicinemedicineHumansImmunosuppression TherapyMonocyteZymosanProteinsGeneral MedicineComplement System ProteinsOligospermiaMolecular biologyRespiratory burstEndocrinologymedicine.anatomical_structurechemistryGenital tractLuminescent MeasurementsAndrologia
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Complement components in relation to macrophage function

1983

ImmunologyPharmacology toxicologyComplement C5aToxicologyComplement componentsOxygen ConsumptionPhagocytosisCell MovementAnimalsHumansMacrophagePharmacology (medical)PharmacologyChemistryMacrophagesComplement C5ThromboxanesComplement C3Complement System ProteinsReceptors ComplementComplement C3bImmunologyComplement C3aProstaglandinsLysosomesFunction (biology)Agents and Actions
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Formation and function of a complement-activating enzyme generated from factors of guinea pig serum and cobra venom

1971

An enzymatic complex can be formed by factors from guinea pig serum and cobra venom, which is able to activate C3 bypassing C1, C4 and C2. Formation and action of the enzyme are described. The action on C3 results in an activation of the terminal complement components and in membrane destruction provided suitable membrane receptors are available.

chemistry.chemical_classificationVenomsCell MembraneGuinea PigsImmunologySnakesComplement System ProteinsBiologyChromatography DEAE-CelluloseEnzymesComplement componentsComplement (complexity)Guinea pigEnzymeMembraneBiochemistrychemistryCell surface receptorAnimalsImmunology and AllergyMagnesiumFunction (biology)Cobra venomEuropean Journal of Immunology
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The modulation of immune complex aggregation by classical pathway-mediated reactions.

1985

Abstract Classical pathway (CP)-triggered reactions of complement-modulated immune complex(IC) aggregation (tetanus toxoid/human anti-tetanus toxoid-IgG; ICs of equivalence) were investigated turbidimetrically during the early stages of reaction. Monospecific Fab'- or Fab-fragments (rabbit) directed against certain complement components were used to block the complement function in normal human serum (NHS). Additionally, parts of the reactions were studied using purified complement components. C1q in serum generated by the addition of EDTA as well as purified C1q were found to increase the IC aggregation. In contrast to C1q, macromolecular C1 is able to inhibit IC aggregation, whereas addit…

EffectorChemistryComplement Activating EnzymesComplement C1qImmunologyToxoidHematologyAntigen-Antibody ComplexComplement System ProteinsComplement C1 Inactivator ProteinsImmune complexComplement componentsComplement (complexity)Classical complement pathwayBiochemistrySolubilityComplement C1ImmunologyImmunology and AllergyHumansComplement Pathway ClassicalComplement ActivationFunction (biology)MacromoleculeImmunobiology
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Influence of Macrophage Activation on the Synthesis of Complement Components C2, C3, C4

1982

Macrophages are a major site of complement synthesis. In the guinea pig production of complement components C1, C2, C4, C3, D, B, and P by peritoneal macrophages has been demonstrated (reviewed in Ref. 1). Whereas marked differences exist in biological activity between resident, elicited and activated macrophages (2), we investigated whether this holds true for the synthesis and secretion of complement components C2, C3, and C4.

Guinea pigChemistryMacrophageBiological activitySecretionComplement (complexity)Cell biologyComplement components
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