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1.
Biol Blood Marrow Transplant ; 17(5): 608-19, 2011 May.
Article in English | MEDLINE | ID: mdl-21176787

ABSTRACT

Attempts to reduce the toxicity of hematopoietic stem cell transplantation have led to the use of various immunosuppressive, yet nonmyeloablative preparative regimens that often include low-dose irradiation. To determine the effects of low-dose irradiation on the dynamics of donor cell engraftment after bone marrow transplantation (BMT), we coupled standard endpoint flow cytometric analysis with in vivo longitudinal bioluminescence imaging performed throughout the early (<10 days) and late (days 10-90) post-BMT periods. To exclude the contribution of irradiation on reducing immunologic rejection, severely immune-deficient mice were chosen as recipients of allogeneic bone marrow. Flow cytometric analysis showed that sublethal doses of total body irradiation (TBI) significantly increased long-term (14 weeks) donor chimerism in the bone marrow compared with nonirradiated recipients (P < .05). Bioluminescence imaging demonstrated that the effect of TBI (P < .001) on chimerism occurred only after the first 7 days post-BMT. Flow cytometric analysis on day 3 showed no increase in the number of donor cells in irradiated bone marrow, confirming that sublethal irradiation does not enhance marrow chimerism early after transplantation. Local irradiation also significantly increased late (but not early) donor chimerism in the irradiated limb. Intrafemoral injection of donor cells provided efficient early chimerism in the injected limb, but long-term systemic donor chimerism was highest with i.v. administration (P < .05). Overall, the combination of TBI and i.v. administration of donor cells provided the highest levels of long-term donor chimerism in the marrow space. These findings suggest that the major effect of sublethal irradiation is to enhance long-term donor chimerism by inducing proliferative signals after the initial phase of homing.


Subject(s)
Bone Marrow Transplantation/immunology , Graft Survival/immunology , Transplantation Chimera/immunology , Animals , Bone Marrow/immunology , Bone Marrow/radiation effects , Bone Marrow Transplantation/methods , Cell Proliferation/radiation effects , Femur/cytology , Femur/immunology , Flow Cytometry , Graft Survival/radiation effects , Hematopoietic Stem Cell Transplantation , Injections, Intravenous , Longitudinal Studies , Luminescence , Mice , Mice, SCID , Mice, Transgenic , Transplantation, Homologous , Whole Body Imaging , Whole-Body Irradiation , X-Rays
2.
Skeletal Radiol ; 34(4): 203-9, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15700181

ABSTRACT

OBJECTIVE: Idiopathic and diabetic-associated muscle necrosis are similar, uncommon clinical entities requiring conservative management and minimal intervention to avoid complications and prolonged hospitalization. An early noninvasive diagnosis is therefore essential. We evaluated the magnetic resonance imaging (MRI) characteristics of muscle necrosis in 14 patients, in eight of whom the diagnoses were confirmed histologically. DESIGN AND PATIENTS: Two experienced musculoskeletal radiologists performed retrospective evaluations of the MRI studies of 14 patients with the diagnoses of skeletal muscle infarction. In 10 cases gadolinium-enhanced (T1-weighted fat-suppressed) sequences were available along with T1-weighted, T2-weighted images and STIR sequences, while in four cases contrast-enhanced images were not available. RESULTS: Eight patients had underlying diabetes and in six patients the cause of the myonecrosis was considered idiopathic. T1-weighted images demonstrated isointense swelling of the involved muscle, with mildly displaced fascial planes. There was effacement of the fat signal intensity within the muscle. Fat-suppressed T2-weighted images showed diffuse heterogeneous high signal intensity in the muscles suggestive of edema. Perifascial fluid collection was seen in eight cases. Subcutaneous edema was present in seven patients. Following intravenous gadolinium administration, MRI demonstrated a focal area of heterogeneously enhancing mass with peripheral enhancement. Within this focal lesion, linear dark areas were seen with serpentine enhancing streaks separating them in eight cases. In two cases, a central relatively nonenhancing mass with irregular margins and peripheral enhancement was noted. The peripheral enhancement involved a significant part of the muscle. No focal fluid collection was noted. CONCLUSIONS: We believe that the constellation of imaging findings on T1- and T2-weighted images and post-gadolinium sequences is highly suggestive of muscle necrosis. We consider certain specific findings on gadolinium-enhanced images to be characteristic. The findings reported here should provide radiologists with useful information in making the diagnosis of skeletal muscle necrosis without resorting to invasive procedures.


Subject(s)
Diabetes Mellitus, Type 1/complications , Magnetic Resonance Imaging/methods , Muscle, Skeletal/pathology , Muscular Diseases/diagnosis , Adult , Aged , Aged, 80 and over , Biopsy , Contrast Media/administration & dosage , Diagnosis, Differential , Edema/diagnosis , Fascia/pathology , Female , Gadolinium DTPA , Humans , Image Enhancement/methods , Male , Middle Aged , Muscular Diseases/complications , Necrosis , Observer Variation , Retrospective Studies
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