TY - JOUR
T1 - The effect of human cord blood therapy on the intestinal tract of lethally irradiated mice
T2 - Possible use for mass casualties
AU - Azzam, Edouard I.
AU - Yang, Zhi
AU - Li, Min
AU - Kim, Soyeon
AU - Kovalenko, Olga A.
AU - Khorshidi, Manoochehr
AU - Ende, Norman
N1 - Funding Information:
We wish to thank Dr Kenneth Klein for his consultation on the intestinal tract lesions, Lynn Baltimore and Philip Petrucelli for assistance in manuscript preparation, and Dr David Lagunoff and Peter Carroll for histological preparations. The Abraham S. Ende Research Foundation supported this investigation. EIA is supported by NASA grant NNJ06HD91G. This paper is in memoriam to the late Dr Milton Ende, who with his brother Dr Norman Ende conducted the first reported successful temporary transplantation of human umbilical cord blood in a patient with leukemia. We also acknowledge the contributions of his staff, and collaborators at the South Side Regional Medical Center, Petersburg, VA (physicians and staff) and the Blood Bank at Grady Memorial Hospital, Atlanta, GA.
PY - 2010/6
Y1 - 2010/6
N2 - Purpose:To evaluate the recovery of the gastrointestinal tract in lethally irradiated mice treated with human cord blood and antibiotics. Materials and methods:A/J mice were randomly assigned to seven study groups, including groups exposed to acute 9 Gy from 137Cs γ-rays to the whole body. Four hours after irradiation, exposed mice were treated with either cord blood nucleated cells, Levaquin, or a combination of both. Weight gain/loss and survival were monitored for 2 months. Upon death or euthanasia, the organs were prepared for molecular and histological analyses. Results:Whereas irradiated mice (n=9) lived 615 days, ∼ 60 of irradiated mice that received the combined treatment (n=7) survived more than 50 days. None of the treated animals developed Graft versus Host disease. All animals lost weight after irradiation; however, the 50+ days-survivors (n=4) gained on average ∼1.8g over their initial weight. Whereas hemorrhagic bone marrow and large areas of transmural necrosis were observed in the bowel of the irradiated mice, the 50+ days-survivors showed recovery of the bone marrow. They behaved normally and had significant but incomplete recovery of the intestinal and colonic mucosa. Human DNA was detected in their organs, particularly in the large intestine. Conclusion:Red cell-depleted cord blood transfusions combined with antibiotic treatment contribute to bone marrow and gastrointestinal recovery in high dose-irradiated mice, and may be an available therapy for mass casualties during radiological emergencies.
AB - Purpose:To evaluate the recovery of the gastrointestinal tract in lethally irradiated mice treated with human cord blood and antibiotics. Materials and methods:A/J mice were randomly assigned to seven study groups, including groups exposed to acute 9 Gy from 137Cs γ-rays to the whole body. Four hours after irradiation, exposed mice were treated with either cord blood nucleated cells, Levaquin, or a combination of both. Weight gain/loss and survival were monitored for 2 months. Upon death or euthanasia, the organs were prepared for molecular and histological analyses. Results:Whereas irradiated mice (n=9) lived 615 days, ∼ 60 of irradiated mice that received the combined treatment (n=7) survived more than 50 days. None of the treated animals developed Graft versus Host disease. All animals lost weight after irradiation; however, the 50+ days-survivors (n=4) gained on average ∼1.8g over their initial weight. Whereas hemorrhagic bone marrow and large areas of transmural necrosis were observed in the bowel of the irradiated mice, the 50+ days-survivors showed recovery of the bone marrow. They behaved normally and had significant but incomplete recovery of the intestinal and colonic mucosa. Human DNA was detected in their organs, particularly in the large intestine. Conclusion:Red cell-depleted cord blood transfusions combined with antibiotic treatment contribute to bone marrow and gastrointestinal recovery in high dose-irradiated mice, and may be an available therapy for mass casualties during radiological emergencies.
KW - Bone marrow
KW - Human umbilical cord blood
KW - Intestinal tract
KW - Ionising radiation
KW - Mass casualties
KW - Stem cells
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U2 - 10.3109/09553000903567987
DO - 10.3109/09553000903567987
M3 - Article
C2 - 20184442
AN - SCOPUS:77952513537
SN - 0955-3002
VL - 86
SP - 467
EP - 475
JO - International Journal of Radiation Biology
JF - International Journal of Radiation Biology
IS - 6
ER -