Assessment of intra-arterial injected autologous bone marrow mononuclear cell distribution by radioactive labeling in acute ischemic stroke

To evaluate the feasibility of monitoring the autologous mononuclear bone marrow (ABMMN) cells implanted into the brain after acute ischemic stroke by the technique of labeling with Tc-99m-HMPAO. A 37-year-old man presented with aphasia, right-side hypoesthesia, and right homonymous hemianopsia afte...

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Published inClinical nuclear medicine Vol. 32; no. 11; p. 839
Main Authors Correa, Patricia Lavatori, Mesquita, Claudio T, Felix, Renata M, Azevedo, Jader C, Barbirato, Gustavo B, Falcão, Carlos Henrique, Gonzalez, Constantino, Mendonça, Maria Lucia, Manfrim, Aquiles, de Freitas, Gabriel, Oliveira, Cristina C, Silva, Daniel, Avila, Dione, Borojevic, Radovan, Alves, Suzana, Oliveira, Jr, Amarino C, Dohmann, Hans F
Format Journal Article
LanguageEnglish
Published United States 01.11.2007
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Summary:To evaluate the feasibility of monitoring the autologous mononuclear bone marrow (ABMMN) cells implanted into the brain after acute ischemic stroke by the technique of labeling with Tc-99m-HMPAO. A 37-year-old man presented with aphasia, right-side hypoesthesia, and right homonymous hemianopsia after an acute ischemic stroke of the left middle cerebral artery. He was included in an autologous bone marrow mononuclear cell-based therapy research protocol about the safety of intra-arterial autologous bone marrow mononuclear cell transplantation for acute ischemic stroke. Nine days after the stroke he received 3.0 x 10(7) ABMMN cells delivered into the left cerebral middle artery via a balloon catheter. Approximately 1% of these cells were labeled with 150 MBq (4 mCi) Tc-99m by incubation with hexamethylpropylene amine oxime (HMPAO). Brain perfusion images with Tc-99m ECD demonstrated hypoperfusion in the left temporal and parietal regions. The perfusion brain images were compared with tomographic views of the brain obtained 8 hours after ABMMN-labeled cell delivery, revealing intense accumulation of the ABMMN-labeled cells in the ipsilateral hemisphere. A whole-body scan was done and showed left brain, liver, and spleen uptake. Our results showed that Tc-99m HMPAO can be used to label ABMMN cells for in vivo cell visualization, and that brain SPECT imaging with labeled ABMMN cells is a feasible noninvasive method for studying the fate of transplanted cells in vivo. Additionally, our findings demonstrate the localization of these intra-arterially injected cells.
ISSN:0363-9762
1536-0229
DOI:10.1097/rlu.0b013e318156b980