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1.
Thyroid ; 14(8): 560-70, 2004 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-15320966

RESUMO

The properties of a human monoclonal antibody to the thyrotropin receptor (TSHR) (M22) with the characteristics of patient sera thyroid stimulating autoantibodies is described. Similar concentrations (pmol/L) of M22 Fab and porcine TSH had similar stimulating effects on cyclic adenosine monophosphate (cAMP) production in TSHR-transfected Chinese hamster ovary cells whereas higher doses of intact M22 immunoglobulin G (IgG) were required to cause the same level of stimulation. Patient sera containing TSHR autoantibodies with TSH antagonist (blocking) activity inhibited M22 Fab and IgG stimulation in a similar way to their ability to block TSH stimulation. Thyroid-stimulating monoclonal antibodies (TSmAbs) produced in mice inhibited 125I-TSH binding and 125I-M22 Fab binding to the TSHR but the mouse TSmAbs were less effective inhibitors than M22. These competition studies emphasized the close relationship between the binding sites on the TSHR for TSH, TSHR autoantibodies with TSH agonist activity, and TSHR autoantibodies with TSH antagonist activity. Recombinant M22 Fab could be produced in Escherichia coli and the recombinant and hybridoma produced Fabs were similarly active in terms of inhibition of TSH binding and cAMP stimulation. The crystal structure of M22 Fab was determined to 1.65 A resolution and is that of a standard Fab although the hypervariable region of the heavy chain protrudes further from the framework than the hypervariable region of the light chain. The M22 antigen binding site is rich in aromatic residues and its surface is dominated by acidic patches on one side and basic patches on the other in agreement with an important role for charge-charge interactions in the TSHR-autoantibody interaction.


Assuntos
Anticorpos Monoclonais/química , Anticorpos Monoclonais/genética , Autoanticorpos/química , Autoanticorpos/genética , Receptores da Tireotropina/imunologia , Animais , Anticorpos Monoclonais/imunologia , Autoanticorpos/imunologia , Células CHO , Clonagem Molecular , Cricetinae , Cristalografia por Raios X , Escherichia coli , Humanos , Fragmentos Fab das Imunoglobulinas/química , Fragmentos Fab das Imunoglobulinas/genética , Fragmentos Fab das Imunoglobulinas/imunologia , Radioisótopos do Iodo , Testes de Neutralização , Estrutura Terciária de Proteína , Proteínas Recombinantes/genética , Proteínas Recombinantes/imunologia , Relação Estrutura-Atividade , Glândula Tireoide/imunologia , Tireotropina/farmacocinética
2.
Dev Med Child Neurol ; 42(2): 116-21, 2000 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-10698329

RESUMO

Postoperative pain in children with spastic cerebral palsy (CP) is often attributed to muscle spasm and is difficult to manage using opiates and benzodiazepines. Adductor-release surgery to treat or prevent hip dislocation in children with spastic CP is frequently performed and is often accompanied by severe postoperative pain and spasm. A double-blinded, randomized, placebo-controlled clinical trial of 16 patients (mean age 4.7 years) with a mainly spastic type of CP (either diplegic or quadriplegic in distribution) was used to test the hypothesis that a significant proportion of postoperative pain is secondary to muscle spasm and, therefore, might be reduced by a preoperative chemodenervation of the target surgical muscle by intramuscular injection of botulinum toxin A (BTX/A). Compared with the placebo, BTX/A was found to be associated with a reduction in mean pain scores of 74% (P<0.003), a reduction in mean analgesic requirements of approximately 50% (P<0.005), and a reduction in mean length of hospital admission of 33% (P<0.003). It was concluded that an important component of postoperative pain in the patient population is due to muscle spasm and this can be managed effectively by preoperative injection with BTX/A. These findings may have implications for the management of pain secondary to muscle spasm in other clinical settings.


Assuntos
Toxinas Botulínicas Tipo A/uso terapêutico , Paralisia Cerebral/complicações , Luxação do Quadril/prevenção & controle , Luxação do Quadril/cirurgia , Contração Muscular/efeitos dos fármacos , Músculo Esquelético/efeitos dos fármacos , Fármacos Neuromusculares/uso terapêutico , Dor Pós-Operatória/prevenção & controle , Toxinas Botulínicas Tipo A/administração & dosagem , Toxinas Botulínicas Tipo A/farmacologia , Paralisia Cerebral/fisiopatologia , Criança , Pré-Escolar , Método Duplo-Cego , Feminino , Luxação do Quadril/etiologia , Humanos , Masculino , Fármacos Neuromusculares/administração & dosagem , Fármacos Neuromusculares/farmacologia , Dor Pós-Operatória/fisiopatologia , Resultado do Tratamento
3.
J Pers Assess ; 48(1): 17-25, 1984 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-16367549

RESUMO

The Personal Orientation Dimensions have been introduced as a refinement and extension of concepts of self-actualizing first measured by the Personal Orientation Inventory. The two inventories are theoretically and empirically compared and contrasted. Overall, there is little to favor the POD. It adds little, if anything, to what the POI provides. The recommendation is that users keep using the POI and not use the POD.

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