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Danielle Paixao CavalcanteCristália Produtos Químicos · Department of RD&I
Danielle Paixao Cavalcante
Doctor of Immunology
About
23
Publications
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Introduction
Danielle Paixao Cavalcante currently works as Cientific Coordinator at the Department of RD&I, Cristália Produtos Químicos. Danielle has a degreen in Biomedical Science (São Paulo State University), PhD in Immunology (University of São Paulo) and Post-doctoral degree in autoimmune diseases (Imperial College and Cardiff University). Currently is in charge of the pre-clinical studies for new drugs development. Their most recent publication is 'Nanostructured SBA-15 Silica: An Effective Protective Vehicle to Oral Hepatitis B Vaccine Immunization'.
Publications
Publications (23)
Due to its physicochemical properties, nanostructured mesoporous SBA-15 silica shows great potential as a vaccine adjuvant. This study evaluated the capacity of SBA-15 to encapsulate/adsorb the recombinant purified HBsAg from the Hepatitis B virus and the immunoresponsiveness of mice orally immunized with HBsAg inside SBA-15. A simulation of small...
An alarming number of fatal accidents involving snakes are annually reported in Africa and most of the victims suffer from permanent local tissue damage and chronic disabilities. Envenomation by snakes belonging to the genus Bitis, Viperidae family, are common in Sub-Saharan Africa. The accidents are severe and the victims often have a poor prognos...
Bothrops lanceolatus, commonly named “Fer-de-Lance”, is the endemic snake of the French Caribbean Island Martinique, where it is responsible for about 20-30 bites per year. B. lanceolatus venom (BlV) causes systemic thrombotic syndrome, and also important local inflammation, involving extensive oedema, pain and haemorrhage from fang punctures. It w...
Introduction: Bothrops lanceolatus, commonly named “Fer-de-Lance”, is the endemic snake of the French Caribbean Island Martinique, where it is responsible for about 20-30 bites per year. B. lanceolatus venom (BlV) causes systemic thrombotic syndrome, resolved by specific antivenom injection, but also important local inflammation, involving extensiv...
Dysregulation of the complement alternative pathway (AP) can cause disease in various organs that may be life-threatening. Severe AP dysregulation can be triggered by autoantibodies to the C3 convertase, termed nephritic factors, which cause pathological stabilisation of the convertase enzyme and confer resistance to innate control mechanisms; unre...
C3 nephritic factors are autoantibodies that prolong the half-life or prevent regulation of the alternative pathway C3 convertase, resulting in uncontrolled complement activation. They are strongly associated with renal disease but their role in pathogenesis remains controversial. Here we optimized and compared a panel of assays to identify and int...
Factor H autoantibodies are found in ∼10% of aHUS patients. Most are associated with complete deficiency of factor H related proteins 1/3 and bind to the C terminal recognition domain. MPGN, like aHUS, is characterised by complement activation. In this study we, therefore, examined the hypothesis that factor H autoantibodies are associated with MPG...
Gene variants in the alternative pathway of the complement system strongly associate with atypical hemolytic uremic syndrome (aHUS), presumably by predisposing to increased complement activation within the kidney. Complement factor H (CFH) is the major regulator of complement activation through the alternative pathway. Factor H-deficient mice trans...
Dense deposit disease (DDD) is strongly associated with the uncontrolled activation of the complement alternative pathway. Factor H (CFH)-deficient (Cfh −/−) mice spontaneously develop C3 deposition along the glomerular basement membrane (GBM) with subsequent development of glomerulonephritis with features of DDD, a lesion dependent on C3 activatio...
Decay-accelerating factor (DAF; CD55) is a membrane protein that regulates complement pathway activity at the level of C3. To test the hypothesis that DAF plays an essential role in limiting complement activation in the arterial wall and protecting from atherosclerosis, we crossed DAF gene targeted mice (daf-1 /) with low-density lipoprotein-recept...
The inflammatory kidney disease membranoproliferative glomerulonephritis type II (MPGN2) is associated with dysregulation of the alternative pathway of complement activation. MPGN2 is characterized by the presence of complement C3 along the glomerular basement membrane (GBM). Spontaneous activation of C3 through the alternative pathway is regulated...
Envenomation by spiders belonging to the Loxosceles genus (brown spider) often results in local dermonecrotic lesions. We have previously shown that Loxosceles sphingomyelinase D (SMase D), the venom component responsible for all the pathological effects, induced the expression of matrix metalloproteinases (MMPs) in rabbits and in human keratinocyt...
Envenomation by arachnids of the genus Loxosceles leads to local dermonecrosis and serious systemic toxicity mainly induced by sphingomyelinases D (SMase D). These enzymes catalyze the hydrolysis of sphingomyelin resulting in the formation of ceramide–phosphate and choline as well as the cleavage of lysophosphatidyl choline generating the lipid med...
Envenomation by the spider Loxosceles (brown spider) can result in dermonecrosis and severe ulceration. We have previously shown that Loxosceles sphingomyelinase D (SMaseD), the enzyme responsible for these pathological effects, induced expression of matrix metalloproteinase-9 (MMP-9), which is possibly one of the main factors involved in the patho...
Envenomation by the spider Loxosceles can result in dermonecrosis and severe ulceration. Our aim was to investigate the role of the complement system and of the endogenous metalloproteinases in the initiation of the pathology of dermonecrosis. Histological analysis of skin of rabbits injected with Loxosceles intermedia venom and purified or recombi...
Loxoscelism is the clinical condition produced by the venom of spiders belonging to the genus Loxosceles, which can be observed as two well-defined clinical variants: cutaneous loxoscelism and systemic or viscerocutaneous loxoscelism. We have recently identified, purified and characterised the toxins (sphingomyelinases) from Loxosceles intermedia v...
On Jan 20, 2004 this sequence version replaced gi:33150239.
On Jan 20, 2004 this sequence version replaced gi:33150241.
Questions
Question (1)
I am performing a phagocytosis assay of inorganic FITC-labelled particles. I am using trypan blue (TB) to quench FITC from the particles that were not internalized. However, the TB is quenching the fluorescence of both, internalized and non-intenalized particles. How can I solve it?