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1.
Vet Immunol Immunopathol ; 106(3-4): 179-96, 2005 Jul 15.
Article in English | MEDLINE | ID: mdl-15963817

ABSTRACT

Multiparameter flow cytometry analysis and specific cluster differentiation (CD) molecules were used to determine the expression profiles of B- and T-cell antigens on lymph node preparations from 59 dogs with generalized or multisystemic lymphoma. Lymph node samples from 11 healthy dogs were labeled to validate the specificity of antibodies and to formulate guidelines for interpretation of the results obtained from lymphoma samples. In normal lymph nodes, T-lymphocytes expressing CD3, CD4, or CD8 beta represented 59+/-11%, 43+/-8%, or 16+/-5% of the total cells, whereas B-lymphocytes expressing either CD21 or surface IgM (IgM) represented 37+/-9% or 14+/-5%, respectively. Small lymphocytes could be distinguished from large lymphocytes by forward light scatter. Of the patient samples 29 different breeds were represented with Golden and Labrador retriever being the most common. The lymphoma samples segregated into three groups based on CD antigen expression. Thirty cases predominantly expressed one or more combinations of CD79a, IgM, and CD21 representing a B-cell lineage. Three B-cell cases also expressed the stem cell antigen, CD34. Sixteen cases expressed one or more combinations of CD3, CD4, and CD8 consistent with a T-cell lineage and CD3+CD4+CD8--phenotype was the most common. Thirteen cases showed a mixed expression profile for T- and B-cell antigens and in three cases CD14 was highly expressed. Clinical response was poorest for T-cell lymphomas. Leukemic states occurred in all three phenotypes; but mixed cell cases had the greatest proportion. Dual immunofluorescence staining confirmed co-expression of T-cell (CD3) and B-cell antigens (CD79a or CD21) on neoplastic lymphocytes of six mixed cell cases. In one mixed cell case, dual immunostaining identified lymphocyte populations that stained mutually exclusive for CD79a and CD3. Six mixed cell lymphomas tested by PCR showed clonality for rearranged antigen receptor. Four cases that were CD79a+CD3+ had TCRgamma chain gene rearrangements, whereas two cases that were CD3+CD8+CD21+ had Ig heavy chain rearrangement. One case expressing multiple CD molecules (CD3+CD8+CD21+CD14+) was PCR negative for both Ig and TCRgamma gene rearrangement and could not be classified into a B- or T-cell lineage. We show for the first time co-expression of B- and T-cell markers on lymphoma cells that had specific T- or B-cell gene rearrangements. These findings suggest that aberrant CD molecule expression is not an uncommon finding in canine lymphomas and is a useful diagnostic marker for malignancy.


Subject(s)
Antigens, CD/metabolism , Dog Diseases/immunology , Leukemia/veterinary , Lymphoma/veterinary , Animals , Antigens, Differentiation, B-Lymphocyte/metabolism , Antigens, Differentiation, T-Lymphocyte/metabolism , B-Lymphocytes/immunology , B-Lymphocytes/pathology , Cell Differentiation , Dog Diseases/genetics , Dog Diseases/pathology , Dogs , Flow Cytometry , Gene Expression Profiling , Gene Rearrangement, B-Lymphocyte , Gene Rearrangement, T-Lymphocyte , Immunophenotyping , Leukemia/genetics , Leukemia/immunology , Leukemia/pathology , Lymphoma/genetics , Lymphoma/immunology , Lymphoma/pathology , Polymerase Chain Reaction , T-Lymphocytes/immunology , T-Lymphocytes/pathology , Tumor Stem Cell Assay
2.
Child Abuse Negl ; 24(1): 25-32, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10660007

ABSTRACT

OBJECTIVE: This study was undertaken to assess academic progress of children 1 to 5 years after graduating from the C. Henry Kempe Center's Therapeutic Preschool Day Treatment Program. METHOD: Information was gathered through chart review; telephone surveys of care providers, relatives, and social service workers; as well questionnaires on all children who attended the therapeutic preschool day treatment program between 1984 and 1989, including the 24 children reported on by Oates, Gray, Schweitzer, Kempe, and Harmon, 1995. RESULTS: Classroom placement was determined for 27 of the 44 graduates (61.4%), 14 of whom (51.9%) were in a regular classroom, 10 (37.0%) in special education, two (7.4%) in residential treatment, and one (3.7%) was receiving home schooling. Twenty-two of the 27 children (81.5%) improved or remained in the same grade and type of classroom as they had been staffed into at the time of their graduation from the preschool day treatment program. Factors thought to affect stability of classroom placement were studied, of which frequency of family moves was the only significant variable. Its significance was in the direction opposite to that expected. The most effective method of locating families was to contact the Department of Social Services who provided information used to find 60% of them. CONCLUSIONS: Intervention in a therapeutic preschool day treatment program was found to be beneficial, as it enabled most of the children to progress appropriately in public school.


Subject(s)
Achievement , Child Abuse, Sexual/therapy , Child Abuse/therapy , Early Intervention, Educational , Child , Child Abuse/psychology , Child Abuse, Sexual/psychology , Child Day Care Centers , Child, Preschool , Colorado , Female , Follow-Up Studies , Hospitals, Pediatric , Humans , Male , Retrospective Studies
3.
J Chromatogr ; 487(2): 385-99, 1989 Feb 24.
Article in English | MEDLINE | ID: mdl-2566618

ABSTRACT

Quantitative analytical methods, based on high-performance liquid chromatography with electrochemical detection, were developed for fenoldopam and its metabolites in human plasma. Two extraction methods, a liquid-liquid extraction method for fenoldopam and its methoxy metabolites and a liquid-solid extraction procedure for the sulfate and glucuronide conjugates of fenoldopam were developed. The extractions can either be performed manually or by robot. The limit of detection for fenoldopam, its sulfate and methoxy metabolites was 0.025, 2 and 0.5 ng/ml, respectively, at a signal to noise ratio of 4. The intra-assay and inter-assay coefficients of variation for both manual and robotic extraction procedures were comparable. These methods were suitably selective and sensitive for pharmacokinetic and metabolic studies of fenoldopam.


Subject(s)
Benzazepines/blood , Vasodilator Agents/blood , Adult , Chromatography, High Pressure Liquid , Electrochemistry , Fenoldopam , Humans , Indicators and Reagents , Male , Robotics
4.
J Clin Pharmacol ; 28(12): 1106-11, 1988 Dec.
Article in English | MEDLINE | ID: mdl-3243927

ABSTRACT

The intraosseous (IO) route provides a rapid and effective alternative venous access in the pediatric population when the conventional intravenous (IV) route cannot be easily obtained. DL-propranolol, a beta-adrenoceptor antagonist, exhibits antiepileptic activity in various animal seizure models. This study assessed the efficacy of IO propranolol in suppressing pentylenetetrazol (PTZ)-induced seizure activity in pigs. Domestic swine (13-20 kg) were prepared for recordings of arterial blood pressure, ECG and electrocortical activity. Seizure activity was induced by pentylenetetrazol (PTZ; 100 mg/kg; IV). Sixty seconds after the onset of seizure activity, the animals either received no drug (control) or propranolol (IV or IO via an 18-gauge spinal needle placed in the right proximal tibia). A transient increase (16.3-50.0%) in the mean arterial blood pressure (MAP) was observed following PTZ administration. Both IO and IV propranolol significantly suppressed the seizure duration (SD) (sec/min interval) at 1 min following drug administration; SD control, 36.3 +/- 4.8; IV propranolol, 12.3 +/- 5.1; IO propranolol, 18.3 +/- 6.0. In addition, both IV and IO propranolol produced a maximal decrease of 32-38% in the basal heart rate; and reduced the transient increase in MAP elicited by PTZ, with no significant effect on the basal MAP. The data demonstrate that 1) propranolol possesses anticonvulsant activity against PTZ-induced seizure in the pig, and 2) the intraosseous route is a rapid and effective alternative venous access for propranolol administration in swine.


Subject(s)
Pentylenetetrazole/antagonists & inhibitors , Propranolol/pharmacology , Seizures/prevention & control , Animals , Blood Pressure/drug effects , Bone and Bones , Dose-Response Relationship, Drug , Electroencephalography , Heart Rate/drug effects , Injections , Injections, Intravenous , Propranolol/administration & dosage , Seizures/chemically induced , Swine , Time Factors
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