Imaging haemopoietic stem cells and microenvironment dynamics through transplantation

被引:0
作者
Williams, Kirsten M. [1 ,2 ,3 ]
Chakrabarty, Jennifer Holter [4 ]
机构
[1] Emory Univ, Dept Pediat, Atlanta, GA 30322 USA
[2] Childrens Healthcare Atlanta, Atlanta, GA 30322 USA
[3] AFLAC Canc & Blood Disorder Ctr, Div Blood & Marrow Transplantat, Atlanta, GA USA
[4] Stephenson Canc Ctr, Dept Med, Div Marrow Transplantat & Cell Therapy, Oklahoma City, OK USA
来源
LANCET HAEMATOLOGY | 2020年 / 7卷 / 03期
基金
美国国家卫生研究院;
关键词
POSITRON-EMISSION-TOMOGRAPHY; VERSUS-HOST-DISEASE; BONE-MARROW UPTAKE; F-18 FDG PET; PROGENITOR CELLS; GENE; VISUALIZATION; ENGRAFTMENT; LYMPHOMA; THERAPY;
D O I
10.1016/s2352-3026(20)30003-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Understanding the subclinical pathway to cellular engraftment following haemopoietic stem cell transplantation (HSCT) has historically been limited by infrequent marrow biopsies, which increase the risk of infections and might poorly represent the health of the marrow space. Nuclear imaging could represent an opportunity to evaluate the entire medullary space non-invasively, yielding information about cell number, proliferation, or metabolism. Because imaging is not associated with infectious risk, it permits assessment of neutropenic timepoints that were previously inaccessible. This Viewpoint summarises the data regarding the use of nuclear medicine techniques to assess the phases of HSCT: pre-transplant homoeostasis, induced aplasia, early settling and engraftment of infused cells, and later recovery of lymphocytes that target cancers or mediate tolerance. Although these data are newly emerging and preliminary, nuclear medicine imaging approaches might advance our understanding of HSCT events and lead to novel recommendations to enhance outcomes.
引用
收藏
页码:E259 / E269
页数:11
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