Exploring Erythropoietin and G-CSF Combination Therapy in Chronic Stroke Patients

被引:19
|
作者
Shin, Yoon-Kyum [1 ,2 ]
Cho, Sung-Rae [1 ,2 ,3 ,4 ]
机构
[1] Yonsei Univ, Coll Med, Dept & Res Inst Rehabil Med, Seoul 03722, South Korea
[2] Yonsei Univ, Coll Med, Brain Korea PLUS Project Med Sci 21, Seoul 03722, South Korea
[3] Yonsei Univ, Coll Med, Rehabil Inst Neuromuscular Dis, Seoul 03722, South Korea
[4] Avison Biomed Res Ctr, Yonsei Stem Cell Res Ctr, Seoul 03722, South Korea
基金
新加坡国家研究基金会;
关键词
erythropoietin; granulocyte-colony stimulating factor; combination therapy; stroke; neuroprotection; COLONY-STIMULATING FACTOR; ANEURYSMAL SUBARACHNOID HEMORRHAGE; RECOMBINANT-HUMAN-ERYTHROPOIETIN; MARROW STEM-CELLS; ISCHEMIC-STROKE; MYELODYSPLASTIC SYNDROMES; DOUBLE-BLIND; RECOVERY ENHANCEMENT; CONTROLLED-TRIAL; GRANULOCYTE;
D O I
10.3390/ijms17040463
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Erythropoietin (EPO) and granulocyte-colony stimulating factor (G-CSF) are known to have neuroprotective actions. Based on previous reports showing the synergistic effects of EPO+G-CSF combination therapy in experimental models, we investigated the safety of EPO+G-CSF combination therapy in patients with chronic stroke. In a pilot study, 3 patients were treated with EPO and G-CSF for 5 consecutive days, with follow-up on day 30. In an exploratory double-blind study, 6 patients were allocated to treatment with either EPO+G-CSF or placebo. Treatment was applied once a day for 5 days per month over 3 months. Participants were followed up for 6 months. To substantiate safety, vital signs, adverse events, and hematological values were measured on days 0, 5, and 30 in each cycle and on day 180. Functional outcomes were determined on day 0 and 180. In the laboratory measurements, EPO+G-CSF combination therapy significantly elevated erythropoietin, CD34(+) hematopoietic stem cells, white blood cells, and neutrophils on day 5 of each cycle. There were no observations of serious adverse events. In the functional outcomes, the grip power of the dominant hand was increased in the EPO+G-CSF treatment group. In conclusion, this exploratory study suggests a novel strategy of EPO+G-CSF combination therapy for stroke patients.
引用
收藏
页数:14
相关论文
共 50 条
  • [41] AMD3100 IN COMBINATION WITH G-CSF RESTORES THE IMPAIRED MOBILIZATION WITH G-CSF ALONE IN THE THALASSEMIC MOUSE MODEL
    Yannaki, E.
    Psatha, N.
    Demertzi, M.
    Athanasiou, E.
    Bougiouklis, D.
    Arsenakis, M.
    Anagnostopoulos, A.
    Fassas, A.
    EXPERIMENTAL HEMATOLOGY, 2009, 37 (09) : S81 - S81
  • [42] Successful mobilization using a combination of plerixafor and G-CSF in pediatric patients who failed previous chemomobilization with G-CSF alone and possible complications of the treatment
    Kyung Taek Hong
    Hyoung Jin Kang
    Nam Hee Kim
    Min Sun Kim
    Ji Won Lee
    Hyery Kim
    Kyung Duk Park
    Hee Young Shin
    Hyo Seop Ahn
    Journal of Hematology & Oncology, 5
  • [43] THE ROLE OF GM-CSF, G-CSF, INTERLEUKIN-3, AND ERYTHROPOIETIN IN MYELODYSPLASTIC SYNDROMES
    GANSER, A
    SEIPELT, G
    HOELZER, D
    AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1991, 14 : S34 - S39
  • [44] Mavorixafor for Patients with Chronic Neutropenic Disorders Treated with G-CSF: Preliminary Response Data and G-CSF Dose Reduction in an Ongoing Phase 2, OpenLabel, Multicenter Study Support Reduction in G-CSF Dosing
    Warren, Julia T.
    Dickerson, Kathryn E.
    Sharathkumar, Anjali A.
    Walter, Jolan E.
    Wilson, David B.
    Adell, Katrina P.
    Chen, Kelly
    Dubuc, Susan
    MacLeod, Rick
    Peters, Katie
    Stewart, Murray
    Taveras, Arthur G.
    Walkovich, Kelly
    BLOOD, 2023, 142
  • [45] Harvesting after G-CSF mobilization: Previous therapy with G-CSF decreases the number of circulating progenitor cells
    Olavarria, E
    Nevado, MI
    Estevez, L
    Prieto, E
    Roman, A
    Soto, C
    Lobo, F
    Paniagua, G
    Llorente, L
    Barbolla, L
    BRITISH JOURNAL OF HAEMATOLOGY, 1996, 93 : 931 - 931
  • [46] Bone Density Measurements in Patients with Severe Chronic Neutropenia On Long-Term G-CSF Therapy.
    Dale, David C.
    Bolyard, Audrey Anna
    DiMeglio, Linda A.
    Marrero, Tracy M.
    Boxer, Laurence A.
    BLOOD, 2009, 114 (22) : 555 - 555
  • [47] G-CSF receptor mutations in patients with severe chronic neutropenia: A step in leukemogenesis?
    Welte, K
    Touw, IP
    BLOOD, 1997, 90 (10) : 1921 - 1921
  • [48] Plerixafor and G-CSF Versus Cyclophosphamide and G-CSF for Stem Cell Mobilization in Patients with Multiple Myeloma
    Nazha, Aziz
    Cook, Rachel
    Vogl, Dan T.
    Mangan, Patricia A.
    Hummel, Kimberly
    Cunningham, Kathleen
    Luger, Selina
    Porter, David
    Schuster, Stephen J.
    O'Doherty, Una
    Sell, Mary
    Siegel, Don L.
    Stadtmauer, Edward A.
    BLOOD, 2009, 114 (22) : 844 - 844
  • [49] The role of G-CSF in chronic obstructive pulmonary disease
    Tsantikos, E.
    Lau, M.
    Maxwell, M.
    Anderson, G.
    Hibbs, M.
    EUROPEAN JOURNAL OF IMMUNOLOGY, 2016, 46 : 376 - 376
  • [50] Superior Stem Cell Mobilization by a Combination of Plerixafor plus G-CSF in Patients with Thalassemia
    Yannaki, Evangelia
    Anagnostopoulos, Achilles
    Karponi, Garyfalia
    Zervou, Fani
    Constantinou, Varnavas
    Psatha, Nikoleta
    Bouinta, Asimina
    Jonlin, Erica
    Papayannopoulou, Thalia
    Stamatoyannopoulos, George
    MOLECULAR THERAPY, 2013, 21 : S11 - S11