DENDRITIC CELL IMMUNIZATION OF PRETERM NEONATES
DENDRITIC CELL IMMUNIZATION OF PRETERM NEONATES
批准号:
6319480
负责人:
KURT R SCHIBLER
金额:
$4.09万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-04-01 至 2001-09-30
关键词:
T lymphocyte antigen presenting cell autologous transplantation biomarker cell adhesion molecules cell component structure /function cell proliferation communicable disease control cord blood cryopreservation cytokine receptors dendritic cells enzyme linked immunosorbent assay flow cytometry histocompatibility human subject iatrogenic disease immunization immunomagnetic separation leukocyte activation /transformation method development newborn human (0-6 weeks) premature infant human tissue /cell culture
中文摘要
描述:(申请人提供)
背景:树突状细胞是一种抗原呈递细胞,
调节适应性免疫的作用。最近,方法已经成为
可以从各种来源分离这些细胞,包括脐带血,
血液、外周血和骨髓。这引发了人们对
这些细胞的潜在治疗用途。
目标:本提案的主要目标是确定
使用脐带血来源的树突状细胞作为治疗肿瘤的试剂的可行性
预防和治疗早产儿传染病。具体
目的是1)表征新鲜分离和培养衍生的树突状细胞,
由脐带血和成人外周血产生的细胞,2)
评估新生儿树突状细胞作为抗原的功能
提呈细胞,以及3)开发自体DC的实用方法
分离、储存和抗原加载。 方法:将树突状细胞
使用免疫磁性分离从脐带血和成人血中获得
技术.新鲜分离和培养的脐带和成人树突状细胞
将比较细胞的谱系标志物的表面表达,主要
组织相容性分子、粘附分子、共刺激分子和
细胞因子受体此外,将评估脐带和成人树突状细胞的
它们的功能能力包括它们诱导幼稚T细胞的能力,
活化和增殖并刺激B细胞成熟为抗体
产生浆细胞。
健康相关性:传染病是一个重大问题,
在新生儿重症监护室住院的极低出生体重(VLBW)婴儿
单位(新生儿重症监护室)。大约25%的极低出生体重新生儿(出生体重
500和1500克)在NICU中至少经历一次记录的
败血症的症状暴露导致住院时间延长
耐药微生物和多种侵入性程序,在存在
免疫不成熟使这些婴儿容易受到医院获得性
感染.树突状细胞可能是理想的免疫载体,
传染源树突状细胞已经显示出呈递细菌和
病毒抗原与T细胞的体外结合。动物研究是令人鼓舞的抗原
脉冲的树突状细胞有效地提供保护性免疫,
水平等于或大于常规佐剂所建立的水平
疫苗。迄今为止,人类研究仅限于I/II期,
在成人志愿者和晚期恶性肿瘤患者中的研究
疾病
英文摘要
DESCRIPTION: (Provided by Applicant)
Background: Dendritic cells are antigen presenting cells that play a critical
role in regulation of adaptive immunity. Recently, methods have become
available to isolate these cells from a variety of sources including cord
blood, peripheral blood, and bone marrow. This has sparked interest in
potential therapeutic use of these cells.
Objectives: The primary objective of this proposal is to determine the
feasibility of using cord blood derived dendritic cells as agents for
prevention and treatment of infectious diseases in preterm infants. Specific
aims are 1) to characterize freshly isolated and culture-derived dendritic
cells generated from umbilical cord blood and adult peripheral blood, 2) to
evaluate the functional capabilities of neonatal dendritic cell as antigen
presenting cells, and 3) to develop practical methods for autologous DC
isolation, storage, and antigen loading. Methods: Dendritic cells will be
obtained from cord blood and adult blood using immunomagnetic separation
techniques. Freshly isolated and culture-derived cord and adult dendritic
cells will be compared for surface expression of lineage markers, major
histocompatibility molecules, adhesion molecules, co-stimulatory molecules and
cytokine receptors. Also, cord and adult dendritic cells will be evaluated for
their functional capabilities including their ability to induce naive T cell
activation and proliferation and to stimulate B cell maturation into antibody
producing plasma cells.
Health Relatedness: Infectious diseases represent a significant problem for
very low birth weight (VLBW) infants hospitalized in Newborn Intensive Care
Units (NICU). Approximately 25 percent of VLBW neonates (birth weight between
500 and 1500 grams) in the NICU experience at least one documented episode of
sepsis during their hospital course. Prolonged hospitalization with exposure
to resistant organisms and multiple invasive procedures, in the presence of
immunologic immaturity renders these infants vulnerable to hospital-acquired
infections. Dendritic cells may be ideal vehicles for immunization against
infectious agents. Dendritic cells have been shown to present bacterial and
viral antigens to T cells in vitro. Animal studies are encouraging as antigen
pulsed dendritic cells are efficacious in providing protective immunity at a
level equal to or greater than that established by conventional adjuvant
vaccines. To date, studies in humans have been limited phase I/II to
investigations in adult volunteers and in patients with advanced malignant
diseases.
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DENDRITIC CELL IMMUNIZATION OF PRETERM NEONATES
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批准号:6536317
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资助金额:$0.16万
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财政年份:1998
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资助金额:$0.16万
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财政年份:1998
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负责人:KURT R SCHIBLER
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依托单位:
DOUBLE BLIND STUDY OF GCSF ADMINISTRATION TO NEONATES WITH NEUTROPENIA
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资助金额:$2.15万
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负责人:KURT R SCHIBLER
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批准号:6245941
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资助金额:$2.15万
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财政年份:1997
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资助金额:$2.15万
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财政年份:1997
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负责人:KURT R SCHIBLER
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ROLE OF NEUTROPHILS AND INFLAMMATORY CYTOKINES IN PREMATURE RDS
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批准号:6245940
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项目类别:
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资助金额:$2.15万
-
财政年份:1997
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负责人:KURT R SCHIBLER
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依托单位:
DOUBLE BLIND STUDY OF GCSF ADMINISTRATION TO NEONATES WITH NEUTROPENIA
-
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资助金额:$2.66万
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财政年份:1997
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负责人:KURT R SCHIBLER
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依托单位:
REGULATION OF GRANULOCYTOPOIESIS IN NEONATES WITH EARLY ONSET BACTERIAL SEPSIS
-
批准号:6276050
-
项目类别:
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资助金额:$2.66万
-
财政年份:1997
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负责人:KURT R SCHIBLER
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依托单位:
MULITCENTER DOUBLEBLIND EFFICACY STUDY OF FILGRASTIM IN NEONATAL SEPSIS
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资助金额:$2.66万
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财政年份:1997
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财政年份:1993
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批准号:2024633
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资助金额:$9.34万
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财政年份:1993
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负责人:KURT R SCHIBLER
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资助金额:$8.26万
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财政年份:1993
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依托单位:
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批准号:2194523
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项目类别:
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资助金额:$8.26万
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财政年份:1993
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负责人:KURT R SCHIBLER
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DEVELOPMENTAL BIOLOGY OF IMMUNO REGULATORY CYTOKINES
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批准号:2194524
-
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资助金额:$9.32万
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财政年份:1993
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依托单位:
海外基金