Evaluating Effects of Age-related Microbiota Modulations in Hematopoietic Stem Cell Transplant Patients

评估与年龄相关的微生物群调节对造血干细胞移植患者的影响

基本信息

  • 批准号:
    9980757
  • 负责人:
  • 金额:
    $ 20.13万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2019
  • 资助国家:
    美国
  • 起止时间:
    2019-08-01 至 2022-04-30
  • 项目状态:
    已结题

项目摘要

Allogeneic hematopoietic stem cell transplant (HCT) has the potential to cure patients with hematologic malignancies. However, HCT is associated with significant treatment related mortality (TRM) ranging from 20- 30%. (1). TRM is particularly high in patients with advanced age (hazard ratio 1.84, age >60 years vs. <20) and decreased physical function (hazard ratio 2.94, bottom quartile vs. top quartile). A major cause of TRM is graft- versus-host disease (GVHD), which affects 40-60% of patients. We hypothesis that age related microbiome changes will affect the HCT clinical outcomes, and in addition to age other factors such as diet, physical activity and the care environment can influence the microbiome profiles as well. Correlations between GVHD and disruptions in the gut microbiota have been reported in several studies, though it remains unclear how the microbiota causes or prevents GVHD. While lengthy hospitalizations are standard for HCT patients, caring for patients in a more normal care environment may preserve the natural microbiota. We hypothesized that shifting the care environment from the hospital to a more normal environment like the home can preserve the gut microbiota, thereby decreasing intestinal inflammation and GVHD. We have successfully piloted home HCT in a phase 1 trial (co-PIs Chao, Sung, clinicaltrials.gov NCT01725022) and have expanded our pilot into a randomized phase 2 study of home vs. standard care (clinicaltrials.gov NCT02218151, co-PIs Chao, Sung) funded by NCI 1R01CA203950 (PI Chao, co-I Sung). While age cannot be changed, other strategies to overcome the negative effects of aging-related microbiome changes can be the use of dietary and physical activity interventions. We have started a Phase I/II, pre- and peri-HCT optimization program (PPOP). PPOP has two pieces: a clinical component (C-PPOP), which establishes a new standard of care for the pre-HCT evaluation of all Duke HCT patients, and a research component (R-PPOP), which includes additional assessments and interventions to optimize health and function including diet and physical activity. In this proposed project we aim to: 1) evaluate the age related microbiome changes and their implications on HCT outcomes including TRM (primary endpoint), infections, GVHD, and immune function; 2) evaluate the effects of a dietary and physical activity intervention on the aged microbiome and implications on HCT outcomes. For this study will be able to utilize existing samples from the Duke Hematologic Malignancies Biorepository. This study can provide new insights into the underlying mechanisms of GVHD in Leukemia and other malignant diseases. If successful, this study will identify the impact of age related microbiome changes on HCT outcomes and the immune system, as well as strategies to target the aged microbiome to promote better outcomes for HCT patients.
同种异体造血干细胞移植(HCT)具有治愈血液病患者的潜力

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

Nelson J. Chao其他文献

3 - Intestinal Microbiota Injury during Allo-Hct is Generalizable across Transplantation Centers and is Associated with Increased Mortality, Broad-Spectrum Antibiotics, and Decreased Calorie Intake
  • DOI:
    10.1016/j.bbmt.2017.12.008
  • 发表时间:
    2018-03-01
  • 期刊:
  • 影响因子:
  • 作者:
    Jonathan U. Peled;Antonio Gomes;Marissa Lubin Buchan;Christoph Stein-Thoeringer;John Slingerland;Ann E. Slingerland;Daniela Weber;Anthony D. Sung;Molly Maloy;Tatanisha Peets;Boglarka Gyurkocza;Sergio A. Giralt;Robert R. Jenq;Ying Taur;Joao Xavier;Eric G. Pamer;Nelson J. Chao;Ernst Holler;Marcel R.M. van den Brink
  • 通讯作者:
    Marcel R.M. van den Brink
Granulocyte colony-stimulating factor "mobilized" peripheral blood progenitor cells accelerate granulocyte and platelet recovery after high-dose chemotherapy.
粒细胞集落刺激因子“动员”外周血祖细胞,加速大剂量化疗后粒细胞和血小板的恢复。
  • DOI:
    10.1182/blood.v81.8.2031.bloodjournal8182031
  • 发表时间:
    1993
  • 期刊:
  • 影响因子:
    20.3
  • 作者:
    Nelson J. Chao;Jeffrey R. Schriber;Kevin Grimes;G. Long;R. Negrin;CathleenM. Raimondi;Sandra J. Horning;S. Brown;Langdon L. Miller;Karl G. Blume
  • 通讯作者:
    Karl G. Blume
Home Sweet Home: Our Experience Providing Immediate Post-Transplant Care to Patients in Their Home
  • DOI:
    10.1016/j.bbmt.2012.11.590
  • 发表时间:
    2013-02-01
  • 期刊:
  • 影响因子:
  • 作者:
    Krista Rowe;Martha Lassiter;Jennifer Loftis;Jennifer Frith;Nelson J. Chao;Deborah Russell;Kimberley Oates;Pamelia Peace;Kari Leonard
  • 通讯作者:
    Kari Leonard
Nicord® Expanded Hematopoietic Progenitor Cells (HPC) Are Capable of Outcompeting the Unmanipulated (UM) Cord Blood Unit and of Prolonged Myeloid and Lymphoid Engraftment Following Myeloablative Dual Umbilical Cord Blood (UCB) Transplantation
  • DOI:
    10.1016/j.bbmt.2012.11.044
  • 发表时间:
    2013-02-01
  • 期刊:
  • 影响因子:
  • 作者:
    Mitchell E. Horwitz;Patrick J. Stiff;Nelson J. Chao;David Rizzieri;Gwynn Long;Keith Sullivan;Cristina Gasparetto;John Chute;Ashley Morris;Carolyn McDonald;Steven Wease;David Snyder;Einat Galamidi-Cohen;Hadas Shoham;Efrat Landau;Etty Friend;Joanne Kurtzberg;Tony Peled
  • 通讯作者:
    Tony Peled
Development of Thioredoxin Monothiol Derivatives for Mitigating Radiation Induced Hematopoietic Injury
  • DOI:
    10.1182/blood-2023-185355
  • 发表时间:
    2023-11-02
  • 期刊:
  • 影响因子:
  • 作者:
    Yubin Kang;Jian Wu;Xiaobei Wang;Parker Mathews;Shaima Jabbar;George William Schaaf;John Olson;Joel Ross;Nelson J. Chao;Mark Cline;Peter B. Heifetz
  • 通讯作者:
    Peter B. Heifetz

Nelson J. Chao的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('Nelson J. Chao', 18)}}的其他基金

Evaluating Effects of Age-related Microbiota Modulations in Hematopoietic Stem Cell Transplant Patients
评估与年龄相关的微生物群调节对造血干细胞移植患者的影响
  • 批准号:
    9808469
  • 财政年份:
    2019
  • 资助金额:
    $ 20.13万
  • 项目类别:
Duke-UNC Chapel Hill Immunotherapy Training Grant
杜克大学-北卡罗来纳大学教堂山免疫治疗培训补助金
  • 批准号:
    9359326
  • 财政年份:
    2017
  • 资助金额:
    $ 20.13万
  • 项目类别:
Duke-UNC Chapel Hill Immunotherapy Training Grant
杜克大学-北卡罗来纳大学教堂山免疫治疗培训补助金
  • 批准号:
    10212334
  • 财政年份:
    2017
  • 资助金额:
    $ 20.13万
  • 项目类别:
Mitigators of Radiation-Induced Endovascular Injury: Targeting Tie2 and Thrombocytopenia
放射引起的血管内损伤的缓解剂:针对 Tie2 和血小板减少症
  • 批准号:
    10170277
  • 财政年份:
    2017
  • 资助金额:
    $ 20.13万
  • 项目类别:
Mitigators of Radiation-Induced Endovascular Injury: Targeting Tie2 and Thrombocytopenia
放射引起的血管内损伤的缓解剂:针对 Tie2 和血小板减少症
  • 批准号:
    9385521
  • 财政年份:
    2017
  • 资助金额:
    $ 20.13万
  • 项目类别:
Smartphone Enabled Point-of-Care Detection of Serum Markers of Liver Cancer
智能手机支持肝癌血清标志物的即时检测
  • 批准号:
    10180910
  • 财政年份:
    2017
  • 资助金额:
    $ 20.13万
  • 项目类别:
Smartphone Enabled Point-of-Care Detection of Serum Markers of Liver Cancer
智能手机支持肝癌血清标志物的即时检测
  • 批准号:
    9933547
  • 财政年份:
    2017
  • 资助金额:
    $ 20.13万
  • 项目类别:
Patient-centered home-based hematopoietic stem cell transplantation
以患者为中心的家庭造血干细胞移植
  • 批准号:
    9922889
  • 财政年份:
    2016
  • 资助金额:
    $ 20.13万
  • 项目类别:
Patient-centered home-based hematopoietic stem cell transplantation
以患者为中心的家庭造血干细胞移植
  • 批准号:
    9266772
  • 财政年份:
    2016
  • 资助金额:
    $ 20.13万
  • 项目类别:
Patient-centered home-based hematopoietic stem cell transplantation
以患者为中心的家庭造血干细胞移植
  • 批准号:
    9078010
  • 财政年份:
    2016
  • 资助金额:
    $ 20.13万
  • 项目类别:

相似国自然基金

靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
  • 批准号:
    JCZRQN202500010
  • 批准年份:
    2025
  • 资助金额:
    0.0 万元
  • 项目类别:
    省市级项目
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
  • 批准号:
    2025JJ70209
  • 批准年份:
    2025
  • 资助金额:
    0.0 万元
  • 项目类别:
    省市级项目
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
  • 批准号:
  • 批准年份:
    2024
  • 资助金额:
    0 万元
  • 项目类别:
    面上项目
甜茶抑制AGE-RAGE通路增强突触可塑性改善小鼠抑郁样行为
  • 批准号:
    2023JJ50274
  • 批准年份:
    2023
  • 资助金额:
    0.0 万元
  • 项目类别:
    省市级项目
蒙药额尔敦-乌日勒基础方调控AGE-RAGE信号通路改善术后认知功能障碍研究
  • 批准号:
  • 批准年份:
    2022
  • 资助金额:
    33 万元
  • 项目类别:
    地区科学基金项目
LncRNA GAS5在2型糖尿病动脉粥样硬化中对AGE-RAGE 信号通路上相关基因的调控作用及机制研究
  • 批准号:
    n/a
  • 批准年份:
    2022
  • 资助金额:
    10.0 万元
  • 项目类别:
    省市级项目
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
  • 批准号:
    81973577
  • 批准年份:
    2019
  • 资助金额:
    55.0 万元
  • 项目类别:
    面上项目
AGE/RAGE通路microRNA编码基因多态性与2型糖尿病并发冠心病的关联研究
  • 批准号:
    81602908
  • 批准年份:
    2016
  • 资助金额:
    18.0 万元
  • 项目类别:
    青年科学基金项目
高血糖激活滑膜AGE-RAGE-PKC轴致骨关节炎易感的机制研究
  • 批准号:
    81501928
  • 批准年份:
    2015
  • 资助金额:
    18.0 万元
  • 项目类别:
    青年科学基金项目

相似海外基金

The Phenomenon of Stem Cell Aging according to Methylation Estimates of Age After Hematopoietic Stem Cell Transplantation
根据造血干细胞移植后甲基化年龄估算干细胞衰老现象
  • 批准号:
    23K07844
  • 财政年份:
    2023
  • 资助金额:
    $ 20.13万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Analysis of Age-dependent Functional Changes in Skeletal Muscle CB1 Receptors by an in Vitro Model of Aging-related Muscle Atrophy
通过衰老相关性肌肉萎缩的体外模型分析骨骼肌 CB1 受体的年龄依赖性功能变化
  • 批准号:
    22KJ2960
  • 财政年份:
    2023
  • 资助金额:
    $ 20.13万
  • 项目类别:
    Grant-in-Aid for JSPS Fellows
Joint U.S.-Japan Measures for Aging and Dementia Derived from the Prevention of Age-Related and Noise-induced Hearing Loss
美日针对预防与年龄相关和噪声引起的听力损失而导致的老龄化和痴呆症联合措施
  • 批准号:
    23KK0156
  • 财政年份:
    2023
  • 资助金额:
    $ 20.13万
  • 项目类别:
    Fund for the Promotion of Joint International Research (International Collaborative Research)
The Effects of Muscle Fatigability on Gait Instability in Aging and Age-Related Falls Risk
肌肉疲劳对衰老步态不稳定性和年龄相关跌倒风险的影响
  • 批准号:
    10677409
  • 财政年份:
    2023
  • 资助金额:
    $ 20.13万
  • 项目类别:
Characterizing gut physiology by age, frailty, and sex: assessing the role of the aging gut in "inflamm-aging"
按年龄、虚弱和性别表征肠道生理学特征:评估衰老肠道在“炎症衰老”中的作用
  • 批准号:
    497927
  • 财政年份:
    2023
  • 资助金额:
    $ 20.13万
  • 项目类别:
Deciphering the role of osteopontin in the aging eye and age-related macular degeneration
破译骨桥蛋白在眼睛老化和年龄相关性黄斑变性中的作用
  • 批准号:
    10679287
  • 财政年份:
    2023
  • 资助金额:
    $ 20.13万
  • 项目类别:
Role of AGE/RAGEsignaling as a driver of pathological aging in the brain
AGE/RAGE信号传导作为大脑病理性衰老驱动因素的作用
  • 批准号:
    10836835
  • 财政年份:
    2023
  • 资助金额:
    $ 20.13万
  • 项目类别:
Elucidation of the protein kinase NLK-mediated aging mechanisms and treatment of age-related diseases
阐明蛋白激酶NLK介导的衰老机制及年龄相关疾病的治疗
  • 批准号:
    23K06378
  • 财政年份:
    2023
  • 资助金额:
    $ 20.13万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Underlying mechanisms of age-related changes in ingestive behaviors: From the perspective of the aging brain and deterioration of the gustatory system.
与年龄相关的摄入行为变化的潜在机制:从大脑老化和味觉系统退化的角度来看。
  • 批准号:
    23K10845
  • 财政年份:
    2023
  • 资助金额:
    $ 20.13万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Targeting Age-Activated Proinflammatory Chemokine Signaling by CCL2/11 to Enhance Skeletal Muscle Regeneration in Aging
通过 CCL2/11 靶向年龄激活的促炎趋化因子信号传导以增强衰老过程中的骨骼肌再生
  • 批准号:
    478877
  • 财政年份:
    2023
  • 资助金额:
    $ 20.13万
  • 项目类别:
    Operating Grants
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了