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1.
J Pediatr Urol ; 15(1): 3-4, 2019 02.
Artículo en Inglés | MEDLINE | ID: mdl-30832992
2.
Pediatr Cardiol ; 27(2): 230-3, 2006.
Artículo en Inglés | MEDLINE | ID: mdl-16391991

RESUMEN

The efficacy of biphasic waveform cardioversion of atrial flutter in pediatric patients has not previously been demonstrated. Cardioversion outcomes were compared in two sequential groups of patients with atrial flutter undergoing transthoracic cardioversion using monophasic and biphasic waveforms at a single pediatric institution. The mean energy required for procedural success was 1.7 +/- 1.2 J/kg in the monophasic group compared to 0.9 +/- 0.6 J/kg in the biphasic group (p = 0.002). The mean number of attempts before achieving procedural success was 1.9 +/- 1.2 for the monophasic group and 1.3 +/- 1.0 for the biphasic group (p = 0.019). Procedure success rate was 89.5% (33/38) in the monophasic group compared to 100% (27/27) in the biphasic group (p = 0.13). Success rate for biphasic waveform cardioversion was 83% (5/6) when using energy less than 0.5 J/kg. These findings provide the impetus for lower starting energies and more widespread use of devices utilizing biphasic waveforms in pediatric patients.


Asunto(s)
Aleteo Atrial/terapia , Cardioversión Eléctrica/métodos , Factores de Edad , Niño , Femenino , Humanos , Masculino , Estudios Retrospectivos , Resultado del Tratamiento
3.
Pediatr Cardiol ; 26(1): 97-100, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-15565271

RESUMEN

This case report discusses a young man with d-transposition of the great arteries who suffered three myocardial infarctions late after his Mustard procedure. The etiology was found to be a coronary embolism, with a mural thrombus in the systemic ventricle as the probable nidus. The risk factors of coronary embolism are discussed, and it is concluded that Mustard patients are at risk for coronary embolization and myocardial infarction, which can be a cause of sudden death.


Asunto(s)
Infarto del Miocardio/etiología , Transposición de los Grandes Vasos/cirugía , Adolescente , Procedimientos Quirúrgicos Cardíacos , Electrocardiografía , Cardiopatías/complicaciones , Humanos , Masculino , Infarto del Miocardio/diagnóstico , Infarto del Miocardio/epidemiología , Factores de Riesgo , Trombosis/complicaciones , Factores de Tiempo
4.
Vaccine ; 22(17-18): 2273-7, 2004 Jun 02.
Artículo en Inglés | MEDLINE | ID: mdl-15149786

RESUMEN

Orally administered recombinant Salmonella vaccines represent an attractive option for mass vaccination programmes against various infectious diseases. Therefore, it is crucial to gather knowledge about the possible impact of preexisiting immunity to carrier antigens on the immunogenicity of recombinant vaccines. Thirteen volunteers were preimmunized with Salmonella typhi Ty21a in order to evaluate the effects of prior immunization with the carrier strain. Then, they received three doses of 1-2 x 10(10) viable organisms of either the vaccine strain S. typhi Ty21a (pDB1) expressing subunits A and B of recombinant Helicobacter pylori urease (n = 9), or placebo strain S. typhi Ty21a (n = 4). Four volunteers were preimmunized and boosted with the vaccine strain S. typhi Ty21a (pDB1). No serious adverse effects were observed in any of the volunteers. Whereas none of the volunteers primed and boosted with the vaccine strain responded to the recombinant antigen, five of the nine volunteers preimmunized with the carrier strain showed cellular immune responses to H. pylori urease (56%). This supports the results of a previous study in non-preimmunized volunteers where 56% (five of nine) of the volunteers showed a cellular immune response to urease after immunisation with S. typhi Ty21a (pDB1).


Asunto(s)
Vacunas Bacterianas/inmunología , Helicobacter pylori/inmunología , Vacunas contra la Salmonella/inmunología , Ureasa/inmunología , Adulto , Anticuerpos Antibacterianos/sangre , Antígenos Bacterianos/inmunología , Vacunas Bacterianas/efectos adversos , Vacunas Bacterianas/genética , Linfocitos T CD4-Positivos/inmunología , Femenino , Infecciones por Helicobacter/prevención & control , Helicobacter pylori/enzimología , Helicobacter pylori/genética , Humanos , Inmunidad Celular , Inmunoglobulina G/sangre , Interferón gamma/análisis , Activación de Linfocitos , Masculino , Plásmidos , Proteínas Recombinantes/genética , Proteínas Recombinantes/inmunología , Vacunas contra la Salmonella/administración & dosificación , Vacunas contra la Salmonella/efectos adversos , Vacunas contra la Salmonella/genética , Salmonella typhi/inmunología , Ureasa/genética , Vacunas Atenuadas/efectos adversos , Vacunas Atenuadas/genética , Vacunas Atenuadas/inmunología , Vacunas Sintéticas/efectos adversos , Vacunas Sintéticas/inmunología
5.
Cell Death Differ ; 11(6): 608-17, 2004 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-14765133

RESUMEN

Marine snails of the genus Aplysia possess numerous bioactive substances. We have purified a 60 kDa protein, APIT (Aplysia punctata ink toxin), from the defensive ink of A. punctata that triggers cell death with profound tumor specificity. Tumor cell death induced by APIT is independent of apoptosis but is characterized by the rapid loss of metabolic activity, membrane permeabilization, and shrinkage of nuclei. Proteome analysis of APIT-treated tumor cells indicated a modification of peroxiredoxin I, a cytoplasmic peroxidase involved in the detoxification of peroxides. Interestingly, knockdown of peroxiredoxin I expression by RNA interference sensitized cells for APIT-induced cell death. APIT induced the death of tumor cells via the enzymatic production of H2O2 and catalase completely blocked APITs' activity. Our data suggest that H2O2 induced stress and the modulation of peroxiredoxins might be a promising approach for tumor therapy.


Asunto(s)
Aplysia/metabolismo , Peróxido de Hidrógeno/farmacología , Toxinas Marinas/farmacología , Neoplasias/tratamiento farmacológico , Oxidantes/farmacología , Peroxidasas/metabolismo , Animales , Apoptosis/efectos de los fármacos , Humanos , Células Jurkat , Peroxirredoxinas
6.
Infect Immun ; 70(11): 6499-503, 2002 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-12379737

RESUMEN

A multiparameter selection of Helicobacter pylori antigens for vaccine development identified 15 candidates, 6 of which are known protective antigens. Two novel antigens with low homology to other organisms (HP0231 and HP0410) were overexpressed and purified with high yields. Both confer protective immunity in the mouse Helicobacter infection model.


Asunto(s)
Antígenos Bacterianos/inmunología , Helicobacter pylori/inmunología , Animales , Antígenos Bacterianos/análisis , Vacunas Bacterianas/inmunología , Modelos Animales de Enfermedad , Femenino , Humanos , Ratones , Ratones Endogámicos BALB C , Linfocitos T/inmunología
7.
Vaccine ; 20(5-6): 845-52, 2001 Dec 12.
Artículo en Inglés | MEDLINE | ID: mdl-11738748

RESUMEN

Helicobacter pylori urease was expressed in the common live typhoid vaccine Ty21a yielding Ty21a(pDB1). Nine volunteers received Ty21a(pDB1) and three control volunteers received Ty21a. No serious adverse effects were observed in any of the volunteers. Ten out of 12 volunteers developed humoral immune responses to the Salmonella carrier as detected by antigen-specific antibody-secreting cells but only two volunteers seroconverted. A total of five volunteers showed responses in one or two out of three assays for cellular responses to the carrier (proliferation, IFN-gamma-secretion, IFN-gamma-ELISPOT). Three of the volunteers that had received Ty21a(pDB1) showed a weak but significant T-cell response to Helicobacter urease, while no volunteer had detectable humoral responses to urease. Ty21a(pDB1) is a suitable prototype to optimize Salmonella-based vaccination for efficient cellular responses that could mediate protective immunity against Helicobacter.


Asunto(s)
Vacunas Bacterianas/farmacología , Helicobacter pylori/enzimología , Helicobacter pylori/inmunología , Salmonella typhi/genética , Ureasa/genética , Ureasa/inmunología , Adolescente , Adulto , Anticuerpos Antibacterianos/biosíntesis , Antígenos Bacterianos/genética , Linfocitos B/inmunología , Vacunas Bacterianas/efectos adversos , Vacunas Bacterianas/genética , Vacunas Bacterianas/inmunología , Método Doble Ciego , Femenino , Expresión Génica , Helicobacter pylori/genética , Humanos , Interferón gamma/biosíntesis , Activación de Linfocitos , Masculino , Seguridad , Linfocitos T/inmunología , Vacunas Sintéticas/efectos adversos , Vacunas Sintéticas/genética , Vacunas Sintéticas/inmunología , Vacunas Sintéticas/farmacología
8.
J Immunol ; 167(10): 5620-7, 2001 Nov 15.
Artículo en Inglés | MEDLINE | ID: mdl-11698433

RESUMEN

Infection of mice with the intracellular bacterium Listeria monocytogenes results in a strong CD8(+) T cell response that is critical for efficient control of infection. We used CD28-deficient mice to characterize the function of CD28 during Listeria infection, with a main emphasis on Listeria-specific CD8(+) T cells. Frequencies and effector functions of these T cells were determined using MHC class I tetramers, single cell IFN-gamma production and Listeria-specific cytotoxicity. During primary Listeria infection of CD28(-/-) mice we observed significantly reduced numbers of Listeria-specific CD8(+) T cells and only marginal levels of specific IFN-gamma production and cytotoxicity. Although frequencies were also reduced in CD28(-/-) mice during secondary response, we detected a considerable population of Listeria-specific CD8(+) T cells in these mice. In parallel, IFN-gamma production and cytotoxicity were observed, revealing that Listeria-specific CD8(+) T cells in CD28(-/-) mice expressed normal effector functions. Consistent with their impaired CD8(+) T cell activation, CD28(-/-) mice suffered from exacerbated listeriosis both after primary and secondary infection. These results demonstrate participation of CD28 signaling in the generation and expansion of Ag-specific CD8(+) T cells in listeriosis. However, Ag-specific CD8(+) T cells generated in the absence of CD28 differentiated into normal effector and memory T cells.


Asunto(s)
Antígenos Bacterianos/inmunología , Antígenos CD28/fisiología , Listeriosis/inmunología , Activación de Linfocitos , Linfocitos T Citotóxicos/inmunología , Animales , Antígenos CD28/genética , Linfocitos T CD4-Positivos/inmunología , Células Cultivadas , Pruebas Inmunológicas de Citotoxicidad , Interferón gamma/biosíntesis , Interleucina-2/biosíntesis , Listeria monocytogenes/inmunología , Listeriosis/microbiología , Ratones , Ratones Noqueados , Péptidos/inmunología
9.
J Immunol ; 167(11): 6480-6, 2001 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-11714815

RESUMEN

N-Formylated (N-f-met) peptides derived from proteins of the intracellular bacterium Listeria monocytogenes generate a protective, H2-M3-restricted CD8 T cell response in C57BL/6 mice. N-f-met peptide-specific CTL were generated in vitro when mice previously immunized with gp96 isolated from donor mice infected with L. monocytogenes were stimulated with these peptides. No significant peptide-specific CTL activity was observed in mice immunized with gp96 from uninfected animals. Masses corresponding to one N-f-met peptide were found by matrix-assisted laser desorption/ionization-mass spectrometry on gp96 isolated from C57BL/6 mice infected with L. monocytogenes, but not on gp96 from noninfected mice. Therefore, bacterial N-f-met peptides from intracellular bacteria can bind to gp96 in the infected host, and gp96 loaded with these peptides can generate N-f-met-peptide-specific CTL. We assume a unique role of gp96 in Ag processing through the H2-M3 pathway.


Asunto(s)
Antígenos de Neoplasias/inmunología , Proteínas Bacterianas/metabolismo , Vacunas Bacterianas/inmunología , Listeria monocytogenes/inmunología , Listeria monocytogenes/metabolismo , Listeriosis/inmunología , N-Formilmetionina/metabolismo , Oligopéptidos/metabolismo , Animales , Antígenos de Neoplasias/administración & dosificación , Antígenos de Neoplasias/metabolismo , Proteínas Bacterianas/inmunología , Vacunas Bacterianas/administración & dosificación , Vacunas Bacterianas/metabolismo , Epítopos de Linfocito T/inmunología , Femenino , Antígenos de Histocompatibilidad Clase II/inmunología , Listeriosis/metabolismo , Activación de Linfocitos/inmunología , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Oligopéptidos/inmunología , Oligopéptidos/aislamiento & purificación , Especificidad de Órganos/inmunología , Unión Proteica/inmunología , Linfocitos T Citotóxicos/inmunología , Linfocitos T Citotóxicos/metabolismo , Células Tumorales Cultivadas
11.
Hum Gene Ther ; 12(6): 659-70, 2001 Apr 10.
Artículo en Inglés | MEDLINE | ID: mdl-11426465

RESUMEN

Although the B cells of chronic lymphocytic leukemia (B-CLL cells) express both tumor-specific peptides and major histocompatibility complex (MHC) class I antigens, they lack the capacity for costimulatory signaling, contributing to their protection against host antitumor immunity. To stimulate CLL-specific immune responses, we sought to transfer the human CD40 ligand (hCD40L) gene to B-CLL cells, using an adenoviral vector, in order to upregulate costimulating factors on these cells. Because efficient gene transduction with adenoviral vectors requires the expression of virus receptors on target cells, including the coxsackievirus B-adenovirus receptors (CAR) and alpha(v) integrins, we cocultured B-CLL cells with human embryonic lung fibroblasts (MRC-5 line). This exposure led to increased expression of integrin alpha(v)beta3 on B-CLL cells, which correlated with higher transduction rates. Using this novel prestimulation system, we transduced B-CLL cells with the hCD40L gene. The Ad-hCD40L-infected cells had higher expression of B7 molecules and induced activation of autologous T cells in vitro, but these T cells could not recognize parental leukemic cells. By contrast, an admixture of Ad-hCD40L-positive cells and leukemic cells transduced with the human interleukin 2 (IL-2) gene produced greater T cell activation than did either immunostimulator population alone. Importantly, this combination generated autologous T cells capable of specifically recognizing parental B-CLL cells. These findings suggest that the combined use of genetically modified CD40L-expressing B-CLL cells in combination with IL-2-expressing B-CLL cells may induce therapeutically significant leukemia-specific immune responses.


Asunto(s)
Ligando de CD40/genética , Interleucina-2/genética , Leucemia Linfocítica Crónica de Células B/inmunología , Linfocitos T/inmunología , Transgenes/genética , Adenoviridae/genética , Células Presentadoras de Antígenos/inmunología , Linfocitos T CD4-Positivos/inmunología , Ligando de CD40/biosíntesis , Linfocitos T CD8-positivos/inmunología , Células Cultivadas , Ensayo de Inmunoadsorción Enzimática , Femenino , Citometría de Flujo , Expresión Génica , Vectores Genéticos , Proteínas Fluorescentes Verdes , Humanos , Inmunoterapia , Integrinas/metabolismo , Interferón gamma/metabolismo , Interleucina-2/biosíntesis , Leucemia Linfocítica Crónica de Células B/terapia , Proteínas Luminiscentes/metabolismo , Linfocitos T Citotóxicos/inmunología , Factores de Tiempo , Transfección
12.
Hum Gene Ther ; 12(7): 833-8, 2001 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-11339899

RESUMEN

To investigate the immune consequences of intraocular administration of modified adenoviral vectors, C57BL/6 normal and retinal degeneration C57BL/6 (rd/rd) mice were immunized with subcutaneous, subretinal, vitreal, or anterior chamber injections of replication-deficient adenovirus (AdV) containing the Escherichia coli beta-galactosidase gene (AdV-LacZ). Fourteen days after the initial inoculation, the animals were immune challenged with an injection of AdV-LacZ in the right ear pinna. Antigen-induced delayed type hypersensitivity (DTH) was measured by determining relative ear swelling. Normal C57BL/6 mice immunized with subretinal, vitreal, or anterior chamber injections did not demonstrate a DTH response. The rd/rd C57BL/6 mice injected in the anterior chamber with the viral construct also did not respond with DTH in a manner similar to normal mice responding to intraocular injection and subsequent challenge. However, the rd/rd C57BL/6 mice immunized by the subretinal or vitreal route did respond to immune challenge with a DTH response. Histologic examination of the eyes showed a lack of infiltration by inflammatory cells. Although these results suggest that the potential for immune consequences is reduced when modified adenoviral vectors are used in the normal ocular environment, these vectors used in the vitreal cavity of rd/rd animals may induce a systemic response to the vectors.


Asunto(s)
Adenoviridae/genética , ADN Viral/administración & dosificación , ADN Viral/inmunología , Ojo/inmunología , Vectores Genéticos/administración & dosificación , Vectores Genéticos/inmunología , Degeneración Retiniana/genética , Animales , ADN Viral/genética , Oído/patología , Ojo/metabolismo , Ojo/patología , Terapia Genética/métodos , Vectores Genéticos/genética , Hipersensibilidad Tardía/inmunología , Hipersensibilidad Tardía/patología , Inflamación/inmunología , Inflamación/patología , Inyecciones/efectos adversos , Inyecciones Subcutáneas/efectos adversos , Operón Lac/genética , Ratones , Ratones Endogámicos BALB C , Ratones Endogámicos C57BL , Degeneración Retiniana/inmunología , Degeneración Retiniana/patología , Degeneración Retiniana/terapia
13.
J Urol ; 165(2): 588-92, 2001 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-11176443

RESUMEN

PURPOSE: We assessed the accuracy of contralateral testis hypertrophy for predicting monorchia in patients with a nonpalpable testis. MATERIALS AND METHODS: From May 1993 to September 1998 we evaluated 60 patients 7 months to 11 years old for a unilateral nonpalpable testis. Four patients were excluded from study who had received human chorionic gonadotropin or had signs of puberty. We correlated contralateral testis hypertrophy, defined as testis volume greater than 2 cc or testis length greater than 2 cm., with presence or absence of the nonpalpable testis. We also recorded the degree to which contralateral testis length less than 2.1 cm. correlated with the presence or absence of the nonpalpable testis. Laparoscopy and open exploration were performed in 52 and 4 cases, respectively. RESULTS: Contralateral testis hypertrophy greater than 2 cm. was noted in 16 patients, including 14 (87.5%) with monorchia and 2 (12.5%) with an intra-abdominal testis. Of the 15 patients with a contralateral measurement of 1.8 to 2.0 cm. 14 had monorchia (93%) and 1 had a tiny ovotestis. Of the 25 patients with a contralateral measurement of less than 1.8 cm. 13 (52%) had testes that were intra-abdominal in 11 and canalicular in 2. The optimal cutoff value for contralateral enlargement was 1.8 cm. (p = 0.00061). The most common laparoscopic finding in patients with contralateral testis hypertrophy greater than 2 cm. was blind ending vessels proximal to the internal ring in 56%. CONCLUSIONS: Contralateral testis hypertrophy is common in patients with a nonpalpable testis. Hypertrophy 1.8 cm. or greater predicts monorchia with an accuracy of about 90%. The finding of contralateral testis hypertrophy provides useful information for preoperative counseling, allowing us to inform parents that the nonpalpable testis is most likely absent. Exploration is still required. Laparoscopy is particularly advantageous in contralateral testis hypertrophy since it was the only procedure required in about half of our cases.


Asunto(s)
Criptorquidismo/diagnóstico , Testículo/patología , Niño , Preescolar , Humanos , Hipertrofia , Lactante , Masculino , Reproducibilidad de los Resultados , Sensibilidad y Especificidad
14.
Infect Immun ; 69(1): 556-8, 2001 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-11119552

RESUMEN

Vaccination of interleukin-4 (IL-4) receptor alpha (IL-4Ralpha) chain-deficient BALB/c mice with Helicobacter pylori urease and cholera toxin or with urease-expressing, live attenuated Salmonella enterica serovar Typhimurium cells revealed that protection against H. pylori infection is independent of IL-4- or IL-13-mediated signals. A comparison of male and female mice suggests a sexual dimorphism in the extent of bacterial colonization that is particularly evident in the absence of the IL-4Ralpha chain.


Asunto(s)
Infecciones por Helicobacter/inmunología , Helicobacter pylori/inmunología , Receptores de Interleucina-4/fisiología , Animales , Toxina del Cólera/inmunología , Femenino , Mucosa Gástrica/microbiología , Interleucina-13/fisiología , Interleucina-4/fisiología , Masculino , Ratones , Ratones Endogámicos BALB C , Caracteres Sexuales , Ureasa/inmunología , Vacunación
15.
Am J Cardiol ; 85(1): 127-30, A10, 2000 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-11078256

RESUMEN

Late-onset pulmonary hypertension is a serious complication of Mustard repair for d-transposition of the great arteries. This debilitating complication occurs in 7% of patients who survive to adulthood, even in the face of normal or near-normal postoperative pulmonary pressure.


Asunto(s)
Hipertensión Pulmonar/etiología , Complicaciones Posoperatorias/etiología , Transposición de los Grandes Vasos/cirugía , Cuidados Posteriores , Factores de Edad , Cateterismo Cardíaco , Preescolar , Ecocardiografía , Estudios de Seguimiento , Humanos , Hipertensión Pulmonar/diagnóstico , Hipertensión Pulmonar/fisiopatología , Lactante , Tamizaje Masivo , Complicaciones Posoperatorias/diagnóstico , Complicaciones Posoperatorias/fisiopatología , Presión Esfenoidal Pulmonar , Factores de Riesgo , Presión Ventricular
16.
Dermatol Surg ; 26(10): 931-5, 2000 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-11050496

RESUMEN

BACKGROUND: Congenital Spitz nevus has been reported previously in the literature, but the histopathologic features have not been examined in detail. OBJECTIVE: To histologically examine and report on congenital Spitz nevus. METHOD: We examined 10 clinically submitted congenital melanocytic nevi that were histopathologically identified as congenital Spitz nevi and compared them to the characteristics seen in acquired Spitz nevus and superficial congenital melanocytic nevus. RESULTS: Of the 10 congenital Spitz nevi, 9 were compound and 1 was dermal. Two showed features of combined Spitz nevus (Spitz and blue). Six cases showed all 16 listed characteristics of acquired Spitz nevus, with two cases having 15 and two cases having 14 characteristics. Of the superficial congenital melanocytic nevus characteristics, all except three cases had all 12 attributes. The one dermal lesion had all the characteristics of the acquired Spitz nevus and all but one of the characteristics of the superficial congenital melanocytic nevus in regards to intradermal findings. CONCLUSIONS: Congenital Spitz nevi are true congenital lesions, with histopathologic features of both acquired Spitz nevus and superficial congenital melanocytic nevus.


Asunto(s)
Nevo de Células Epitelioides y Fusiformes/congénito , Nevo de Células Epitelioides y Fusiformes/patología , Neoplasias Cutáneas/congénito , Neoplasias Cutáneas/patología , Adolescente , Adulto , Biopsia con Aguja , Niño , Preescolar , Femenino , Humanos , Inmunohistoquímica , Masculino , Nevo de Células Epitelioides y Fusiformes/cirugía , Estudios Retrospectivos , Sensibilidad y Especificidad , Neoplasias Cutáneas/cirugía
17.
EMBO J ; 19(20): 5332-43, 2000 Oct 16.
Artículo en Inglés | MEDLINE | ID: mdl-11032801

RESUMEN

Infection of cell cultures with Neisseria gonorrhoeae results in apoptosis that is mediated by the PorB porin. During the infection process porin translocates from the outer bacterial membrane into host cell membranes where its channel activity is regulated by nucleotide binding and voltage-dependent gating, features that are shared by the mitochondrial voltage-dependent anion channel (VDAC). Here we show that porin is selectively and efficiently transported to mitochondria of infected cells. Prevention of porin translocation also blocked the induction of apoptosis. Mitochondria of cells treated with porin both in vitro and in vivo were depleted of cytochrome c and underwent permeability transition. Overexpression of Bcl-2 blocked porin-induced apoptosis. The release of cytochrome c occurred independently of active caspases but was completely prevented by Bcl-2. Our data suggest that the Neisseria porin can, like its eukaryotic homologue, function at the mitochondrial checkpoint to mediate apoptosis.


Asunto(s)
Apoptosis , Proteínas de la Membrana Bacteriana Externa/metabolismo , Mitocondrias/metabolismo , Mitocondrias/microbiología , Neisseria gonorrhoeae/metabolismo , Porinas/metabolismo , Apoptosis/efectos de los fármacos , Proteínas de la Membrana Bacteriana Externa/antagonistas & inhibidores , Proteínas de la Membrana Bacteriana Externa/farmacología , Inhibidores de Caspasas , Caspasas/metabolismo , Permeabilidad de la Membrana Celular/efectos de los fármacos , Grupo Citocromo c/metabolismo , Activación Enzimática/efectos de los fármacos , Células HeLa , Humanos , Inmunohistoquímica , Activación del Canal Iónico , Células Jurkat , Mitocondrias/efectos de los fármacos , Mitocondrias/enzimología , Dilatación Mitocondrial/efectos de los fármacos , Neisseria gonorrhoeae/patogenicidad , Porinas/antagonistas & inhibidores , Porinas/farmacología , Transporte de Proteínas/efectos de los fármacos , Proteínas Proto-Oncogénicas c-bcl-2/genética , Proteínas Proto-Oncogénicas c-bcl-2/metabolismo , Canales Aniónicos Dependientes del Voltaje , Proteína bcl-X
18.
Am J Pathol ; 157(4): 1405-12, 2000 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-11021842

RESUMEN

To generate animal models of retinoblastoma that closely resemble metastatic and nonmetastatic human disease for the purposes of examining tumor biology and developing alternate treatments, human retinoblastoma cell lines were injected into the vitreal cavities of immunodeficient mice. Two reproducible animal models with contrasting biological behaviors analogous to human retinoblastoma have been developed. The Y79 retinoblastoma model demonstrated specific tumor evolution similar to that seen in human invasive and metastatic disease. Y79 retinoblastoma cells formed intraocular tumors that were initially confined to the vitreal cavity. Tumors progressively invaded the retina, subretinal space, choroid, optic nerve head, and anterior chamber of the eye. Tumors progressed into the subarachnoid space and focally invaded the brain. Metastases were detected in the contralateral optic nerve. Large tumors developed extraocular extensions. The histology of the tumors showed a poorly differentiated pattern with high mitotic rate, foci of necrosis, and calcification. The WERI-Rb model more closely resembled nonmetastatic human retinoblastoma. WERI- Rb tumors were localized in the eye with only anterior choroidal invasion at late stages. To examine potential biological differences in vitro, the retinoblastoma cell lines were cocultured with adherent choroid cells or adherent glioma cells which represent the targets of invasive retinoblastoma in vivo. Consistent with the in vivo observations, Y79 cells but not WERI-Rb cells adhere specifically to both the choroidal and the glioma cell lines.


Asunto(s)
Neoplasias de la Retina/patología , Retinoblastoma/patología , Retinoblastoma/secundario , Animales , Adhesión Celular , Línea Celular , Coroides/citología , Modelos Animales de Enfermedad , Ojo/patología , Femenino , Glioma/patología , Haplorrinos , Humanos , Lactante , Ratones , Trasplante de Neoplasias , Ratas , Neoplasias de la Retina/fisiopatología , Retinoblastoma/fisiopatología
19.
Clin Transplant ; 14(4 Pt 2): 421-6, 2000 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-10946782

RESUMEN

Antilymphocytic agent induction (ALAI), with antithymocyte globulin or monoclonal antibody, is generally used in renal transplantation (TX) to spare renal allografts with poor initial function from the toxic effects of cyclosporine (CsA) and/or to augment immunosuppression (IS) in the patient at a high risk for early rejection. ALAI, unfortunately, increases the cost of TX and the risk to the patient, having been associated with many adverse side effects. An IS protocol, which results in a low incidence of early rejection while using less CsA and ALAI, is a worthwhile goal. We compare our experience with mycophenolate mofetil (MMF), CsA, and prednisone (MMFCP; n = 62) to our azathioprine (AZA), CsA, and prednisone (AZACP; n = 50) triple-drug IS, with and without ALAI. The patient characteristics for age, race, first TX, cadaveric donor, pediatric recipient, and dialysis in the first post-op week (DGF) were not different for the MMFCP versus AZACP groups. There were more females in the MMFCP group (51.6% versus 30.0%, p = 0.022). We report that rejection-free survival at 6 months (RF6) was better in the MMFCP versus AZACP group (83.9% versus 60.0%, p = 0.005). Less ALAI and CsA were used in the MMFCP patients. At 1 year, actuarial graft survival was 91.9% in the MMFCP group and 81.9% in the AZACP group (p = 0.116). Actuarial 1-year patient survivals were not different in the two patient groups. In the sub-population of patients with DGF, the RF6 in the MMFCP (n = 13) group was 92.3% versus 57.1% in the AZACP (n = 14) group (p = 0.041). The reduction in early rejection episodes in the patients on MMFCP with DGF was accomplished while using half as much ALAI and lower CsA doses and levels. The African-American recipient sub-population on MMFCP also demonstrated an improvement in RF6 while using less ALAI and CsA (78.6% versus 48.0%, p = 0.022). We conclude that the use of MMF-based triple-drug IS results in fewer rejection episodes while allowing for lower CsA levels and less ALAI, even in patients with delayed graft function.


Asunto(s)
Suero Antilinfocítico/uso terapéutico , Ciclosporina/uso terapéutico , Rechazo de Injerto/prevención & control , Inmunosupresores/uso terapéutico , Trasplante de Riñón , Ácido Micofenólico/análogos & derivados , Prednisona/uso terapéutico , Análisis Actuarial , Adolescente , Adulto , Anciano , Niño , Preescolar , Femenino , Humanos , Trasplante de Riñón/fisiología , Masculino , Persona de Mediana Edad , Ácido Micofenólico/uso terapéutico , Factores de Tiempo
20.
J Am Coll Cardiol ; 36(1): 255-61, 2000 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-10898443

RESUMEN

OBJECTIVES: The purpose of this study was to determine long-term outcome in adults with congenitally corrected transposition of the great arteries (CCTGA), with particular emphasis on systemic ventricular dysfunction and congestive heart failure (CHF). BACKGROUND: Patients with CCTGA have the anatomical right ventricle as their systemic pumping chamber, with ventricular dysfunction and CHF being relatively common in older adults. METHODS: Retrospective analysis of records of 182 patients from 19 institutions were reviewed to determine current status and possible risk factors for systemic ventricular dysfunction and CHF. Factors considered included age, gender, associated cardiac defects, operative history, heart block, arrhythmias and tricuspid (i.e., systemic atrioventricular) regurgitation (TR). RESULTS: Both CHF and systemic ventricular dysfunction were common in groups with or without associated cardiac lesions. By age 45, 67% of patients with associated lesions had CHF, and 25% of patients without associated lesions had this complication. The rates of systemic ventricular dysfunction and CHF were higher with increasing age, the presence of significant associated cardiac lesions, history of arrhythmia, pacemaker implantation, prior surgery of any type, and particularly with tricuspid valvuloplasty or replacement. Aortic regurgitation (a previously unreported problem) was also relatively common in this patient population. CONCLUSIONS: Patients with CCTGA are increasingly subject to CHF with advancing age; this complication is extremely common by the fourth and fifth decades. Tricuspid (systemic atrioventricular) valvular regurgitation is strongly associated with RV (anatomical right ventricle connected to aorta in CCTGA patients; systemic ventricle in CCTGA) dysfunction and CHF; whether it is causative or a secondary complication remains speculative.


Asunto(s)
Insuficiencia Cardíaca/etiología , Transposición de los Grandes Vasos/complicaciones , Disfunción Ventricular/etiología , Adulto , Factores de Edad , Ecocardiografía Doppler , Femenino , Estudios de Seguimiento , Insuficiencia Cardíaca/epidemiología , Insuficiencia Cardíaca/fisiopatología , Humanos , Incidencia , Masculino , Pronóstico , Estudios Retrospectivos , Factores de Riesgo , Factores Sexuales , Transposición de los Grandes Vasos/diagnóstico por imagen , Transposición de los Grandes Vasos/fisiopatología , Disfunción Ventricular/epidemiología , Disfunción Ventricular/fisiopatología
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