Vll Edition of Quincke´s Scholarship: Lecture Highlights

Introduction: Quincke´s Scholarship deals with themes related to neuroinmunology and the complement system. Objective: Describe the most recent advances of the Vll Edition of Quincke´s Scholarship. Methods: Publications pertaining to Quincke´s Scholarship were selected and revised from the work group of the Central Lab of Cerebrospinal fluid (LABCEL). Results: The principal topic was the C1q protein; initiator of the clasic complement pathway. From the analisis of the molecular concentration of this protein, its transference and the correlations between the concentration of C1q protein in cerebrospinal fluid (LCR) and the quotient of albumin (QAlb) between LCR and plasma it is hypothesized that an intratecal synthesis of the C1q in patients with a disfunction of the blood-brain barrier. The most recently discovered pathway in the activation of the complement is the lectin pathway. The diffusion of the MASP-3 protein from blood to LCR is proof that the MASP-3 is synthesized in the leptomeninges. The reibergram is useful to evaluate the inmune response in patients with: neurological manifestations caused by the dengue virus, and patients with multiple sclerosis. Conclusions: The Vll Edition of Quincke´s Scholarship dealt with C1q protein and recently discovered themes of the lectin pathway and the use of the reibergram(AU)

Kinetics-like equation for cerebrospinal fluid-blood diffusion models

Introduction: The diffusion of proteins from the blood to the cerebrospinal fluid is influenced by its molecular weight and by the intrinsic properties and biological properties of the protein. Methods: Paired samples of serum and cerebrospinal fluid were taken from normal subjects to quantify albumin and proteins of the lectin pathway of the complement system. The distribution of these with regard to the value of QAlbúmin = (Albumin in serum / albumin in cerebrospinal fluid) was evaluated because this protein is used as a marker of the passage of the barrier. Results: It was observed that some of these describe a saturation pattern which resembles the curves that describe the Michaelis-Menten reaction of enzymatic activity. This led to the consideration of two constants that will help to characterize the behavior of these proteins by spreading to the cerebrospinal fluid: the maximum Q of the protein, which is the maximum proportion found empirically between the concentrations in blood and cerebrospinal fluid and the value Kcdw which is the value of the average diffusion speed of Q albumin when the semi-maximal value of the Q of the protein under study is obtained. Conclusions: Empirically obtained constants will help the characterization and differentiation of the diffusion of these new proteins as they pass from the blood to the cerebrospinal fluid(AU)