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Hematopoiesis and Stem Cells: Increased numbers of circulating hematopoietic stem/progenitor cells are chronically maintained in patients treated with the CD49d blocking antibody natalizumab

机译:造血和干细胞:长期接受CD49d阻断抗体那他珠单抗治疗的患者循环造血干/祖细胞数量不断增加

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摘要

Blockade of CD49d-mediated lymphocyte trafficking has been used therapeutically for certain autoimmune diseases, such as multiple sclerosis (MS). In addition to negative effects on the trafficking of mature lymphocytes to sites of inflammation, CD49d blockade in mice and monkeys rapidly mobilizes hematopoietic stem/progenitor cells (HSPCs) capable of short- and long-term engraftment. Here we aimed to ascertain the effects of treatment with antifunctional anti-CD49d antibody in humans (MS patients receiving infusions of the CD49d-blocking antibody natalizumab) on levels of circulating HSPCs after a single dose of antibody or after long-term treatment. On average, 6-fold elevated levels of circulating CD34+ cells and colony-forming unit-culture (CFU-C) were achieved within 1 day of the first dose of natalizumab, and similar levels were continuously maintained under monthly natalizumab infusions. The blood of natalizumab-treated subjects also contained SCID-repopulating cells. The fate of these circulating HSPCs and their clinical relevance for MS patients remains to be determined.
机译:CD49d介导的淋巴细胞运输的阻断已在治疗上用于某些自身免疫性疾病,例如多发性硬化症(MS)。除了对成熟淋巴细胞向炎症部位的运输产生不利影响外,小鼠和猴子中的CD49d阻断作用还迅速动员了能够短期和长期植入的造血干/祖细胞(HSPC)。在此,我们旨在确定在单剂量抗体治疗或长期治疗后对人类(接受CD49d阻断抗体那他珠单抗输注的MS患者)抗循环抗CD49d抗体治疗对循环HSPCs水平的影响。在第一代那他珠单抗治疗的1天内,循环CD34 + 细胞和集落形成单位培养(CFU-C)的平均水平升高了6倍,并且持续维持相似的水平每月接受那他珠单抗输注。那他珠单抗治疗的受试者的血液中也含有SCID繁殖细胞。这些循环HSPC的命运及其与MS患者的临床相关性尚待确定。

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