T CELL RECONSTITUTION AFTER STEM CELL AUTOGRAFTING
干细胞自体移植后 T 细胞重建
基本信息
- 批准号:6613452
- 负责人:
- 金额:$ 29.93万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1999
- 资助国家:美国
- 起止时间:1999-07-01 至 2004-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION: (Verbatim from Investigator's abstract):
Background: The recovery of CD4 T cells after high-dose chemo/radiotherapy in
adult patients with cancer or autoimmune diseases is very slow (years) and may
result in only limited T cell repertoire. A similar problem exists in AIDS
patients treated with highly active anti-retroviral therapy. With the ultimate
goal of designing strategies to improve the T cell regeneration after T
lymphocytopenia, here we propose to study the mechanism of the T cell
regeneration.
Hypothesis: We hypothesize that after T-lymphocytopenia a substantial number of
regenerating T cells originate from hemopoietic progenitors in young
individuals whereas only few, if any, T cells originate from hemopoietic
progenitors in older individuals. Instead, in the older individuals, the vast
majority of T cells originate from the expansion of preexisting T cells.
Methods: This hypothesis will be tested in severely lymphocytopenic patients
with autoimmune diseases who have received high-dose chemo/radiotherapy plus
anti-thymocyte globulin followed by autologous transplantation of hemopoietic
(CD34+) cells. An extremely limited number of T cell clones survive such
transplant conditioning/ CD34+ cell purification. Therefore, it is relatively
easy (easier and more informative than in patients with only moderate T
lymphocytopenia) to track down the fate of the surviving T cell clones and to
detect T cells newly generated from hemopoietic progenitors post-transplant,
using the following techniques: spectratyping, sequencing of the T cell
receptor genes within a single spectratyping band, and quantifying T cells that
contain T cell receptor-rearrangement excision circles (TREC).
Outcome: If the above hypothesis is true, the repertoire of T cells, that is
severely limited within the first several months after transplant, will later
diversify in young (less than 5-years-old) whereas it will stay severely
limited in older (greater than 45-years-old) patients. Also, if the hypothesis
is true, the number of TREC-containing T cells post-transplant will be
significantly higher in the young compared to the older patients. This will
give impetus for developing strategies to enable older patients to generate T
cells from hemopoietic progenitors, e.g., using thymopoietic cytokines or
thymus grafting.
描述:(逐字摘自研究者摘要):
项目成果
期刊论文数量(4)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Transgene expression by a large fraction of dendritic cells following autologous transplantation of retrovirally transduced CD34 cells.
逆转录病毒转导的 CD34+ 细胞自体移植后,大部分树突状细胞进行转基因表达。
- DOI:10.1089/scd.2006.15.619
- 发表时间:2006
- 期刊:
- 影响因子:4
- 作者:Storek,Jan;Kiem,Hans-Peter
- 通讯作者:Kiem,Hans-Peter
Early recovery of CD4 T cell receptor diversity after "lymphoablative" conditioning and autologous CD34 cell transplantation.
“淋巴清除”调理和自体 CD34 细胞移植后 CD4 T 细胞受体多样性的早期恢复。
- DOI:10.1016/j.bbmt.2008.09.013
- 发表时间:2008
- 期刊:
- 影响因子:0
- 作者:Storek,Jan;Zhao,Zhao;Liu,Yiping;Nash,Richard;McSweeney,Peter;Maloney,DavidG
- 通讯作者:Maloney,DavidG
Normal interleukin-7 (IL7) levels and normal IL7 response to CD4 T lymphopenia in patients with multiple sclerosis and systemic sclerosis.
多发性硬化症和系统性硬化症患者的正常白介素 7 (IL7) 水平以及对 CD4 T 淋巴细胞减少症的正常 IL7 反应。
- DOI:10.1016/j.clim.2006.05.016
- 发表时间:2006
- 期刊:
- 影响因子:0
- 作者:Storek,Jan;Nash,RichardA;McSweeney,PeterA;Furst,DanielE;Sullivan,KeithM
- 通讯作者:Sullivan,KeithM
Long-term response of juvenile idiopathic arthritis after conditioning with 8 Gy total body irradiation followed by autologous peripheral blood stem cells: case report.
幼年特发性关节炎经 8 Gy 全身照射后自体外周血干细胞调理后的长期反应:病例报告。
- DOI:10.1111/j.1399-3046.2009.01129.x
- 发表时间:2010
- 期刊:
- 影响因子:1.3
- 作者:Woolfrey,Ann;Storek,Jan;Bowyer,Suzanne;Nelson,Robert;Robertson,Michael;Wallace,Carol
- 通讯作者:Wallace,Carol
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JAN STOREK其他文献
JAN STOREK的其他文献
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{{ truncateString('JAN STOREK', 18)}}的其他基金
Preclinical Testing of Interleukin-7 in Primates
Interleukin-7 在灵长类动物中的临床前测试
- 批准号:
6319291 - 财政年份:2001
- 资助金额:
$ 29.93万 - 项目类别:
Preclinical Testing of Interleukin-7 in Primates
Interleukin-7 在灵长类动物中的临床前测试
- 批准号:
6528196 - 财政年份:2001
- 资助金额:
$ 29.93万 - 项目类别:
Preclinical Testing of Interleukin-7 in Primates
Interleukin-7 在灵长类动物中的临床前测试
- 批准号:
6644818 - 财政年份:2001
- 资助金额:
$ 29.93万 - 项目类别:
T CELL RECONSTITUTION AFTER STEM CELL AUTOGRAFTING
干细胞自体移植后 T 细胞重建
- 批准号:
6017567 - 财政年份:1999
- 资助金额:
$ 29.93万 - 项目类别:
T CELL RECONSTITUTION AFTER STEM CELL AUTOGRAFTING
干细胞自体移植后 T 细胞重建
- 批准号:
6374275 - 财政年份:1999
- 资助金额:
$ 29.93万 - 项目类别:
T CELL RECONSTITUTION AFTER STEM CELL AUTOGRAFTING
干细胞自体移植后 T 细胞重建
- 批准号:
6510906 - 财政年份:1999
- 资助金额:
$ 29.93万 - 项目类别:
T CELL RECONSTITUTION AFTER STEM CELL AUTOGRAFTING
干细胞自体移植后 T 细胞重建
- 批准号:
6170806 - 财政年份:1999
- 资助金额:
$ 29.93万 - 项目类别:
B CELL TRANSFUSIONS FOR POSTBMT IMMUNE DEFICIENCY
B 细胞输注治疗 TBMT 后免疫缺陷
- 批准号:
2112477 - 财政年份:1995
- 资助金额:
$ 29.93万 - 项目类别:
B CELL TRANSFUSIONS FOR POSTBMT IMMUNE DEFICIENCY
B 细胞输注治疗 TBMT 后免疫缺陷
- 批准号:
2895387 - 财政年份:1995
- 资助金额:
$ 29.93万 - 项目类别:
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