The Characterization of CD34+ Derived Mast Cell Precursors
Collecte de données
Données recueillies dès le début de l'étude - ProspectiveTroubles d'Activation des Mastocytes+5
+ Maladies du Système Immunitaire
+ Néoplasmes
Cas témoins
Analyse de profils avec et sans la maladie pour comprendre ce qui pourrait l'avoir favorisée.Résumé
Date de début de l'étude : 3 décembre 1997
Date à laquelle le premier participant a commencé l'étude.The purpose of this protocol is to obtain large numbers of CD34+ cells from the peripheral blood of healthy volunteers and patients with systemic mastocytosis or other related allergic, hematological, and immunological conditions by leukapheresis for culture and characterization of mast cell progenitor cells and their response to various cytokines and anti-mitotic agents. Healthy volunteers and patients will be adults of both sexes from 18 to 70 years of age. Granulocyte colony stimulating factor (G-CSF) will be administered to healthy volunteers at dose of 10 mcg/kg/day as a subcutaneous dose daily for 5 days not to exceed 960mcg. Patients will receive Plerixafor at a dose of 0.24 mg/kg as a single subcutaneous dose not to exceed 24mg the night before leukapheresis as a mobilizing agent for CD34+ cells. In identified patients where leukapheresis yield is considered adequate without stimulation by the principal investigator, leukapheresis may proceed without stimulation. Healthy volunteers will undergo a single leukapheresis at day 7, and patients will undergo a single leukapheresis at day 3 or 4. This is not a therapeutic protocol and does not involve reinfusion of any manipulated cells, viruses or DNA constructs back into human subjects.
Protocole
Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.202 participants à inclure
Nombre total de participants que l'essai clinique vise à recruter.Cas témoins
Éligibilité
Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.Tout sexe
Le sexe biologique des participants éligibles à s'inscrire.De 18 à 70 ans
Tranche d'âge des participants éligibles à participer.Volontaires sains autorisés
Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.Conditions
Pathologie
Critères
SUBJECT INCLUSION CRITERIA: Healthy Volunteers must: Be 18-70 years of age Be healthy Have adequate peripheral venous access Have normal renal function (creatinine less than or equal to 1.5mg/dL; less than or equal to 1 plus proteinuria) Have normal hepatic function (bilirubin less than or equal to 1.5 mg/dL) Have normal hematologic function (WBC greater than or equal to 3000/mm(3); granulocytes greater than or equal to 1500/mm(3) ; platelets greater than or equal to 175,000; hemoglobin greater than or equal to 12.5 g/dL) Patients must: Be 18-70 years of age Have mast cell hyperplasia compatible with a diagnosis of systemic mastocytosis (applicable to systemic mastocytosis patients only) or other allergic, hematologic, or immunologic condition Have adequate peripheral venous access or be willing to have a central line placed. First be admitted as inpatients under an existing NIH protocol Have preserved renal function (creatinine less than or equal to 2 mg/dL; less than or equal to 2 plus proteinuria) Have preserved hepatic function (bilirubin less than or equal to 1.5 mg/dL) Have preserved hematologic function (WBC greater than or equal to 3000/mm(3); granulocytes greater than or equal to 1500/mm(3) ; platelets greater than or equal to 175,000; hemoglobin greater than or equal to 12.5 g/dL) All female subjects of childbearing potential: May be enrolled if using effective contraception Have a negative serum or urine pregnancy test determined within 72 hours before beginning Plerixafor or G-CSF administration SUBJECT EXCLUSION CRITERIA: All subjects must not meet any of the following criteria: Healthy Volunteers and patients must not: Have active bacterial, fungal or viral infections Have viral screens positive for HIV or hepatitis B or C Be pregnant or lactating Have a history of autoimmune disease such as rheumatoid arthritis, vasculitis, pyoderma gangrenosum or similar disorder Have any condition, which in the judgment of the investigator, might place the subject at undue risk Healthy Volunteers with any of the following will be excluded: Splenomegaly, pulmonary fibrosis and other related conditions Use of any investigative drugs within the past 12 months Have a significant coagulation disorder Systemic Mastocytosis and Mast Cell Related Condition Patients with any of the following will be excluded: Patients taking any other growth factors, cytokines or investigative drugs Patients who are hemodynamically unstable (blood pressure systolic of lower than 105 or diastolic lower than 65)
Plan de l'étude
Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.2 groupes d'intervention sont désignés dans cette étude
Cette étude ne comporte pas de groupe placebo.
Groupes de traitement
Objectifs de l'étude
Objectifs principaux
Centres d'étude
Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.Cette étude comporte 1 site
National Institutes of Health Clinical Center
Bethesda, United StatesOuvrir National Institutes of Health Clinical Center dans Google Maps