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金奈的地中海贫血、生物样本库基础设施与个性化干细胞疗法

Thalassemia, biobanking infrastructures, and personalized stem cell therapies in Chennai.

作者信息

Panwar Amishi

机构信息

Department of Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.

出版信息

Front Sociol. 2023 Jul 27;8:1057220. doi: 10.3389/fsoc.2023.1057220. eCollection 2023.

Abstract

Thalassemia and leukemia and related blood disorders are approved for blood stem cell transplants in India, for a stem cell transplant to be successful, the human leukocyte antigen (HLA) complex located on the arm of chromosome six must be a match between the cord blood donor and the recipient. In the quest to find an exact blood stem cell match for an individual, the HLA becomes the node at the center of community genetics where the HLA match is sought (not necessarily successful) in the extended family, the same caste, language, and ethnic (both national and the diaspora) groups. By considering thalassemia as a case study, how do we understand personalized stem cell therapies within biobanking infrastructures in Chennai? How do social categories get entwined with biological materials like cord blood?

摘要

地中海贫血、白血病及相关血液疾病在印度被批准可进行造血干细胞移植。要使干细胞移植成功,位于第六条染色体臂上的人类白细胞抗原(HLA)复合体必须在脐带血供体和受体之间相匹配。在为个体寻找精确的造血干细胞匹配的过程中,HLA成为群体遗传学核心的节点,人们在大家庭、相同种姓、语言及族裔(包括国内和侨民群体)中寻找HLA匹配(不一定成功)。以地中海贫血为例,我们如何理解钦奈生物样本库基础设施中的个性化干细胞疗法?社会类别是如何与脐带血等生物材料交织在一起的?

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8e2/10415100/7a37c94f10c9/fsoc-08-1057220-g0001.jpg

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