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1.
Medisan ; 24(2)mar.-abr. 2020.
Artículo en Español | LILACS, CUMED | ID: biblio-1098396

RESUMEN

Se presenta el caso clínico de un anciano de 84 años de edad, fumador, con diagnóstico de cáncer de pulmón en etapa IV, quien fue incluido en el ensayo clínico de fase III para ser tratado con racotumumab. Se observó mejoría clínica y del estado general del paciente, pues según la escala funcional concluyó el estudio con ECOG 0. Por tanto, es oportuno destacar que esta vacuna incrementa la supervivencia de los afectados por cáncer de pulmón de células no pequeñas recurrentes o en estadios avanzados.


The case report of a 84 years elderly smoker, is presented with diagnosis of lung cancer in stage IV who was included in the phase III clinical trial to be treated with racotumomab. Clinical improvement and recovery of the patient's general state was observed, because according to the functional scale the study concluded with ECOG 0. Therefore, it is opportune to highlight that this vaccine increases the survival of those affected by recurrent non-small cells lung cancer or in advanced stages.


Asunto(s)
Inmunoterapia Activa , Carcinoma de Pulmón de Células no Pequeñas/terapia , Ensayo Clínico Fase III , Supervivencia
3.
Rev. cuba. med. mil ; 47(1): 23-32, ene.-mar. 2018. tab
Artículo en Español | LILACS, CUMED | ID: biblio-960591

RESUMEN

Introducción: en los últimos años la biología de los meningiomas cerebrales ha comenzado a entenderse mejor. La inmunoterapia activa contra el factor de crecimiento epidérmico es un concepto emergente, en el que se propone manipular la respuesta inmune del individuo, para generar anticuerpos específicos contra el factor de crecimiento epidérmico, capaces de bloquear la unión ligando-receptor y por consiguiente la señalización a través de este último. El receptor del factor de crecimiento epidérmico está sobrexpresado en este tipo de tumor. Objetivo: estimar la sobrevida libre de progresión de la entidad clínica y su relación con algunas variables socio-demográficas y terapéuticas seleccionadas. Métodos: se realizó un estudio descriptivo, transversal, en 25 pacientes portadores de meningiomas, tratados con un anticuerpo monoclonal humanizado (AcM h-R3) (nimotuzumab), en el Hospital Provincial Docente Clínico Quirúrgico Saturnino Lora de Santiago de Cuba, en el período comprendido entre el 1 de diciembre del 2013 y el 30 de noviembre del 2015. Resultados: el conjunto de pacientes incluidos en el estudio (n= 25) se caracterizó por el predominio del sexo femenino (60 por ciento), edad de 50 y más años (68 por ciento), piel blanca (48 por ciento) y escala de Karnofsky de 100 puntos (84 por ciento). El tiempo medio libre de progresión fue de 17 ± 8,6 meses. Conclusiones: fueron identificadas las principales características de la supervivencia libre de progresión del meningiomas en pacientes vacunados con AcM h-R3 y el tiempo fue como promedio de alrededor de año y medio(AU)


Introduction: in recent years the biology of brain meningiomas has begun to be better understood. Active immunotherapy against epidermal growth factor is an emerging concept, in which it is proposed to manipulate the immune response of the individual, to generate specific antibodies against epidermal growth factor, capable of blocking the ligand / receptor binding and therefore signaling through the latter. The epidermal growth factor receptor is overexpressed in this type of tumor. Objective: to estimate the progression free survival and its relation with some selected socio-demographic and therapeutic variables. Methods: a descriptive, cross-sectional study was conducted in 25 patients with meningiomas, treated with a humanized monoclonal antibody (mAb h-R3) (Nimotuzumab), in the Provincial Clinical-Surgical Teaching Hospital Saturnino Lora of Santiago de Cuba, from December 1, 2013 to November 30, 2015. Results: the group of patients included in the study (n= 25), was characterized by the predominance of females (60 percent), age 50 and over (68 percent), white skin (48 percent) and Karnofsky scale of 100 points (84 percent). The mean progression-free time was 17 ± 8.6 months. Conclusions: the main characteristics of progression-free survival of meningiomas were identified in patients vaccinated with mAb h-R3 and the progression-free time reached almost of a year and a half(AU)


Asunto(s)
Humanos , Femenino , Persona de Mediana Edad , Inmunoterapia Activa/métodos , Factor de Crecimiento Epidérmico/uso terapéutico , Meningioma/epidemiología , Estudios Epidemiológicos , Epidemiología Descriptiva
4.
Rev. Pesqui. (Univ. Fed. Estado Rio J., Online) ; 9(3): 627-633, jul.-set. 2017. tab
Artículo en Inglés, Portugués | LILACS, BDENF | ID: biblio-869943

RESUMEN

Objective: To analyze the socio-demographic profile of reported hepatitis B and immunization against the disease. Methods: Study Hepatitis B notification data in the surveillance of a Minas Gerais’ municipality, from 2007 to 2015, conducted at the Labor Education Program for Health descriptive and analytical statistics, with significance level of p < 0.05. Results: 132 cases and two deaths were notified. The age of the reported cases ranged from zero to 87 years, average 35.8 (± 14.0) years. More frequently for men (52.3%) and with low education (64.8%). Most of them did not vaccinate (81.8%) and had positive result of HSBsAg serology (90.1%); immunization was not linked to the socio-demographic profile (p > 0.05). Conclusion: Age, education and gender were not associated with immunization, vaccination schedule and the HSBsAg test. The absence of vaccination among the notified suggests need for health education among the population, orienting the possibility of protection by immunization.


Objetivo: Analisar o perfil sociodemográfico dos notificados para hepatite B e a imunização contra a doença. Métodos: Estudo com dados de notificação de hepatite B na vigilância epidemiológica do município de Minas Gerais, entre 2007 a 2015, conduzido no Programa de Educação pelo Trabalho para a Saúde. Estatística descritiva e analítica, com nível de significância p < 0,05. Resultados: Notificaram-se 132 casos e dois óbitos. A idade dos notificados variou de zero a 87 anos, média de 35,8 (± 14,0) anos. Maior frequência para homens (52,3%) e baixa escolaridade (64,8%). A maioria não vacinou (81,8%) e teve resultado da sorologia HSBsAg positivo (90,1%); a imunização não se associou ao perfil sociodemográfico (p > 0,05). Conclusão: Idade, escolaridade e sexo não foram associados à imunização, ao esquema vacinal ou ao teste HSBsAg. A ausência de vacinação entre os notificados sugere a necessidade de educação em saúde junto à população, orientando-a sobre possibilidade de proteção pela imunização.


Objetivo: Analizar el perfil sociodemográfico reportado de hepatitis B y la inmunización contra la enfermedad. Métodos: Estudio de datos de notificación de la hepatitis B en la vigilancia del municipio de Minas Gerais, de 2007 a 2015, realizadas en el Programa de Educación para el Trabajo de estadística descriptiva y analítica de la Salud, con un nivel de significación de p<0,05. Resultados: 132 casos fueron notificados; dos muertes. La edad del reportado varió de cero a 87 años, con una media de 35,8 (± 14,0) años. Con mayor frecuencia entre los hombres (52,3%) y baja educación (64,8%). La mayoría no vacunados (81,8%) y tuvo resultado positivo de HSBsAg serología (90,1%); la inmunización no vinculado al perfil sociodemográfico (p > 0,05). Conclusión: La edad, la educación y el sexo no se asociaron con la inmunización, calendario de vacunación y la prueba HSBsAg. La ausencia de vacunación entre los notificados sugiere la necesidad de educación para la salud entre la población, orientando la posibilidad de protección mediante la vacunación.


Asunto(s)
Lactante , Preescolar , Niño , Adolescente , Adulto Joven , Adulto , Persona de Mediana Edad , Anciano , Anciano de 80 o más Años , Cobertura de Vacunación , Hepatitis B/epidemiología , Hepatitis B/mortalidad , Hepatitis B/prevención & control , Inmunoterapia Activa , Perfil de Salud , Vacunas contra Hepatitis B , Brasil , Monitoreo Epidemiológico
5.
Int. arch. otorhinolaryngol. (Impr.) ; 20(1): 6-12, Jan.-Mar. 2016. tab, graf
Artículo en Inglés | LILACS | ID: lil-773505

RESUMEN

Introduction The relevance of allergic rhinitis is unquestionable. This condition affects people s quality of life and its incidence has increased over the last years. Objective Thus, this study aims to analyze the effectiveness of subcutaneous injectable immunotherapy in cases of nasal itching, sneeze, rhinorrhea and nasal congestion in allergic rhinitis patients. Methods In the present study, the same researcher analyzed the records of 281 patients. Furthermore, the researchers identified allergens through puncture cutaneous tests using standardized extracts containing acari, fungi, pet hair, flower pollen, and feathers. Then, the patients underwent treatment with subcutaneous specific immunotherapy, using four vaccine vials for desensitization, associated with environmental hygiene. The authors analyzed conditions of nasal itching, sneeze, rhinorrhea, and nasal congestion throughout the treatment, and assigned them with a score ranging from zero (0), meaning absence of these symptoms to three (3), for severe cases. The symptoms were statistically compared in the beginning, during, and after treatment. Results In this study, authors analyzed the cases distribution according to age and the evolution of symptomatology according to the scores, comparing all phases of treatment. The average score for the entire population studied was 2.08 before treatment and 0.44 at the end. These results represent an overall improvement of ±79% in symptomatology of allergic rhinitis in the studied population. Conclusion The subcutaneous immunotherapy as treatment of allergic rhinitis led to a reduction in all symptoms studied, improving the quality of life of patients, proving itself as an important therapeutic tool for these pathological conditions.


Asunto(s)
Humanos , Masculino , Femenino , Preescolar , Niño , Adolescente , Adulto , Persona de Mediana Edad , Anciano , Adulto Joven , Inmunoterapia Activa , Rinitis Alérgica , Signos y Síntomas , Desensibilización Inmunológica , Inyecciones Subcutáneas
6.
International Journal of Mycobacteriology. 2016; 5 (1): 34-43
en Inglés | IMEMR | ID: emr-177660

RESUMEN

Objective/background: There is an urgent need for a more effective vaccine against Mycobacterium tuberculosis [Mtb]. Although CD4+ T cells play a central role in host immunity to Mtb, recent evidence suggests a critical role of CD8+ T cells in combating Mtb. In the present study, we have predicted HLA antigen class I binding peptides of DosR operon using an in-silico approach. This method is useful as an initial computational filtration of probable epitopes based on their binding ability and antigenicity


Methods: CD8+ epitopes were predicted by software NetMHC 3.4 and BIMAS. Self-peptides were found and excluded by indigenously developed Perl script. Antigenicity of promiscuous peptides was predicted using a Vaxijen server. The top Vaxijen scoring antigenic peptides were docked to globally relevant HLA allele using CABS dock and Hex program


Results: A total of 1436 overlapping nonamer peptides were generated which gave 46 promiscuous epitopes, 25 were predicted to be antigenic. Rv2627 epitope "SAFRPPLV" which gave the highest Vaxijen score of 1.9157 and showed binding to all the three HLA loci. The top Vaxijen scoring antigenic peptides were docked and had significant interactions with residues of the HLA class I molecule indicating them to be good cytotoxic T lymphocyte epitopes


Conclusion: Our study has generated several promiscuous antigenic peptides capable of binding to major histocompatibility complex class I with high affinity. These epitopes can become part of a postexposure multivalent subunit vaccine upon experimental validation


Asunto(s)
Proteínas Bacterianas , Regulón , Proteínas Quinasas , Epítopos de Linfocito T , Inmunoterapia Activa , Linfocitos T CD8-positivos , Mycobacterium tuberculosis , Tuberculosis
7.
An. bras. dermatol ; 88(1): 32-40, fev. 2013. tab, graf
Artículo en Inglés | LILACS | ID: lil-667938

RESUMEN

BACKGROUND: The histopathology and immune responses of the healing process of leishmaniasis are still poorly studied. OBJECTIVES: This study aimed to examine the histopathological and immunological aspects of lesions of patients with cutaneous leishmaniasis before and after different therapeutic methods. METHODS: We studied 23 individuals grouped according to the treatments: Glucantime, Glucantime + Leishvacin and Glucantime + Leishvacin associated with Bacillus Calmette-Guerin. For analysis of the histopathological changes present in the dermis and epidermis, histological sections were stained with hematoxylin and eosin. The samples were immunostained before and after treatment to analyze the expression of interferon (IFN)-γ, interleukin (IL) 12, IL-10 and IL-4. RESULTS: Before treatment the presence of intense infiltrates of mononuclear cells was noticed and after treatment, even with a diagnosis of clinical cure, the subjects still showed a moderate inflammatory process. In the immunohistochemical analyses, we noticed a difference between the cytokines, with increased expression of cytokines IFN-γ and IL-12 compared to IL 10 and IL-4, both before and after treatment and, comparatively, the difference in this expression was more intense before treatment. However, the cytokine expression analyzed by treatment group showed no statistically significant difference. CONCLUSION: We conclude that a clinical cure does not always coincide with the histopathological ...


FUNDAMENTOS: A histopatologia e as respostas imunológicas do processo de cura da leishmaniose são ainda pouco estudadas. OBJETIVOS: Este estudo teve como objetivo avaliar os aspectos histopatológicos e imunológicos das lesões de pacientes com leishmaniose tegumentar, antes e após diferentes métodos terapêuticos. MÉTODOS: Foram estudados 23 indivíduos agrupados de acordo com os tratamentos: Glucantime, Glucantime + Leishvacin e Glucantime + Leishvacin associado com Bacilo Calmette-Guerin. Para a análise das alterações histopatológicas presentes na derme e epiderme, cortes histológicos foram corados com hematoxilina e eosina. Para avaliar a expressão de interferon (IFN)-γ, interleucina (IL) 12, IL-10 e IL-4 foi utilizada a técnica de imuno-histoquímica antes e após o tratamento. RESULTADOS: Antes do tratamento houve um intenso infiltrado de células mononucleares, após o tratamento, mesmo com um diagnóstico de cura clínica, apresentou-se ainda um moderado processo inflamatório. Na análise imuno-histoquímica, notamos uma diferença entre as citocinas, com expressão aumentada de citocinas IFN-γ e IL-12 em comparação com IL-10 e IL-4 tanto antes quanto depois do tratamento, e comparativamente, a diferença nesta expressão mostrou-se mais intensa antes do tratamento. No entanto, a expressão das citocinas analisadas por grupo de tratamento não mostraram diferenças ...


Asunto(s)
Adolescente , Adulto , Anciano , Niño , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Antiprotozoarios/uso terapéutico , Citocinas/biosíntesis , Inmunoterapia Activa/métodos , Leishmaniasis , Adyuvantes Inmunológicos/uso terapéutico , Vacuna BCG/uso terapéutico , Inmunohistoquímica , Leishmania/inmunología , Vacunas contra la Leishmaniasis/uso terapéutico , Leishmaniasis/tratamiento farmacológico , Leishmaniasis/inmunología , Leishmaniasis/patología , Meglumina/uso terapéutico , Compuestos Organometálicos/uso terapéutico , Estudios Retrospectivos , Resultado del Tratamiento , Cicatrización de Heridas/efectos de los fármacos
8.
In. Lopes, Ademar; Chammas, Roger; Iyeyasu, Hirofumi. Oncologia para a graduação. São Paulo, Lemar, 3; 2013. p.238-243, tab. (Oncologia para a graduação).
Monografía en Portugués | LILACS | ID: lil-692003
9.
Rev. méd. Costa Rica Centroam ; 69(604): 455-459, oct.-dic. 2012.
Artículo en Español | LILACS | ID: lil-762525

RESUMEN

El virus del papiloma humano es una de las infecciones de transmisión sexual más comunes, se encuentra asociado con varias enfermedades desde cáncer cervical y anal, hasta verrugas genitales. Sus particulares inmunológicas le permiten subsistir en algunos pacientes y causar enfermedades malignas. Con la aprobación de la vacuna tetravalente contra el VPH los médicos poseemos una nueva arma en la prevención primaria contra el cáncer cervical, las verrugas genitales y el cáncer anal. Este trabajo revisa los conocimientos actuales sobre esta vacuna y sus indicaciones en medicina general.


Asunto(s)
Humanos , Papiloma , Vacunas Virales , Inmunoterapia Activa , Enfermedades Bacterianas de Transmisión Sexual/inmunología , Enfermedades Virales de Transmisión Sexual/diagnóstico , Enfermedades Virales de Transmisión Sexual/patología , Enfermedades Virales de Transmisión Sexual/terapia , Costa Rica
10.
Perionews ; 6(1): 89-93, jan. 2012.
Artículo en Portugués | LILACS | ID: lil-688080

RESUMEN

A cárie dentária é uma doença de rápida progressão, podendo levar a destruição dos elementos dentários. Neste artigo, os autores fazem uma revisão da literatura sobre o estado atual da vacina anticárie. São discutidos os principais mecanismos de ação da vacina anticárie em modelos animais e sua aplicabilidade em humanos, revelando qual impacto pode ser observado na prevenção da doença cárie. Estudos clínicos futuros devem ser incentivados para o total esclarecimento da vacina anticárie e do seu mecanismo de ação.


Asunto(s)
Humanos , Masculino , Femenino , Caries Dental/inmunología , Caries Dental/prevención & control , Inmunoterapia Activa , Odontología Preventiva/métodos , Vacunas/uso terapéutico
11.
Chinese Journal of Integrated Traditional and Western Medicine ; (12): 766-769, 2012.
Artículo en Chino | WPRIM | ID: wpr-288524

RESUMEN

<p><b>OBJECTIVE</b>To study the immunoregulation effects of Tiaomian No. 3 (TM3) for recurrent spontaneous abortion (RSA) caused by shortage of blocking antibodies.</p><p><b>METHODS</b>Totally 61 patients with RSA caused by shortage of blocking antibodies were randomly assigned to the treatment group (31 cases) and the control group (30 cases) by lot method. Patients in the treatment group were treated with TM3, while those in the control group were treated with active immunotherapy using lymphocytes of their spouses. The therapeutic course for all was 3 months. Another 10 healthy females in the same age ranges were recruited as the healthy control group. The blocking antibodies (Ab1), anti-idiotypic antibodies (Ab2), T-lymphocyte cell subsets (CD4 and CD8), serum interleukin 10 (IL-10), and macrophage colony-stimulating factor (M-CSF) levels were determined before and after treatment.</p><p><b>RESULTS</b>(1) After treatment the positive conversion rate of Ab1 and/or Ab2 was 87.1% (27/31) in the treatment group and 86.7% (26/30) in the control group, showing no statistical difference (P > 0.05). (2) In the two groups, CD4 decreased and CD8 increased. The CD4/CD8 ratio was in the normal level after treatment, showing statistical difference when compared with before treatment (P < 0.05). (3) In the two groups, IL-10 and M-CSF levels were higher after treatment, showing statistical difference when compared with before treatment (P < 0.05). (4) The 1-year conception rate was 58.1% (18/31) in the treatment group, significantly higher than that in the control group (46.7%, 14/30, P < 0.05).</p><p><b>CONCLUSIONS</b>TM3 could promote the positive conversion rate of Ab1, promote the production of IL-10 and M-CSF cytokines, thus strengthening the protection for fetus by the mother and the normal maintenance for pregnancy. The 1-year successful pregnancy rate obviously increased in the treatment group.</p>


Asunto(s)
Adulto , Femenino , Humanos , Embarazo , Aborto Habitual , Quimioterapia , Alergia e Inmunología , Anticuerpos Antiidiotipos , Anticuerpos Bloqueadores , Relación CD4-CD8 , Medicamentos Herbarios Chinos , Farmacología , Usos Terapéuticos , Inmunoterapia Activa , Interleucina-10 , Sangre , Factor Estimulante de Colonias de Macrófagos , Sangre , Fitoterapia , Subgrupos de Linfocitos T
12.
Chinese Journal of Biotechnology ; (12): 261-266, 2012.
Artículo en Chino | WPRIM | ID: wpr-304495

RESUMEN

Heat-shock protein gp96 associates with antigenic peptides derived from tumor and virus. Exogenous gp96-peptide complexes are taken up by antigen-presenting cells through interaction with its receptor CD91 on the cell surface, and cross-present antigenic peptides to MHC class I molecules by a peptide relay line in the endoplasmic reticulum for specific T-cell activation. Meanwhile, gp96 has been shown to initiate innate immune responses through interaction with toll-like receptor 2 and toll-like receptor 4. Recent studies have shown a gp96-mediated immune balance between CTL and Tregs. With the further understanding of counteracting immunosuppressive mechanisms in gp96-induced cellular immune responses, and establishment of high level production of recombinant gp96 by the yeast, gp96 appears to be a promising candidate for designing effective therapeutic vaccines against tumor and infectious diseases.


Asunto(s)
Animales , Humanos , Enfermedades Transmisibles , Terapéutica , Proteínas de Choque Térmico , Alergia e Inmunología , Usos Terapéuticos , Inmunoterapia Activa , Métodos , Neoplasias , Terapéutica , Linfocitos T Reguladores , Alergia e Inmunología
13.
Invest. clín ; 52(4): 365-375, dic. 2011. ilus
Artículo en Inglés | LILACS | ID: lil-659226

RESUMEN

A patient with localized cutaneous leishmaniasis due to Leishmania (Leishmania) amazonensis infection was treated with an antigen containing heat-killed L. (L.) amazonensis promastigotes plus BCG. Expression of T-cell differentiation, memory and senescence receptors markers were analyzed on T cell subpopulations, in order to establish the correlation between the percentages of expression of these receptors and his clinical status, at different stages of his follow up. The following case reports on the achievement of a successful clinical outcome with complete resolution after receiving immunotherapy. A thorough clinical and immunological follow up supporting the healing process of this patient’s lesion is presented in detail.


Un paciente con leishmaniasis cutánea localizada producida por Leishmania (Leishmania) amazonensis fue tratado con un antígeno compuesto por promastigotes de L. (L.) amazonensis muertos por calor combinado con BCG. Se analizó la expresión de distintos receptores de diferenciación, de memoria y de senescencia en las subpoblaciones de células T, con el fin de establecer una relación entre los porcentajes de expresión de dichos receptores y la clínica del paciente en diferentes momentos del seguimiento. Se reporta en este caso un resultado exitoso, con resolución completa de la lesión después de recibir la inmunoterapia, y se presenta en detalle un seguimiento clínico e inmunológico completo durante el proceso de curación.


Asunto(s)
Adulto , Humanos , Masculino , Antígenos de Protozoos/uso terapéutico , Vacuna BCG/uso terapéutico , Inmunoterapia Activa , Leishmania mexicana/inmunología , Leishmaniasis Cutánea/terapia , Enfermedades Profesionales/terapia , Vacunas Antiprotozoos/uso terapéutico , Antígenos de Protozoos/administración & dosificación , Antígenos de Protozoos/inmunología , Argentina/epidemiología , Vacuna BCG/administración & dosificación , Explotaciones Pesqueras , Inmunidad Celular , Memoria Inmunológica , Inyecciones Intradérmicas , Úlcera de la Pierna/etiología , Úlcera de la Pierna/parasitología , Leishmania mexicana/crecimiento & desarrollo , Leishmaniasis Cutánea/epidemiología , Leishmaniasis Cutánea/inmunología , Leishmaniasis Cutánea/parasitología , Enfermedades Profesionales/inmunología , Enfermedades Profesionales/parasitología , Vacunas Antiprotozoos/administración & dosificación , Vacunas Antiprotozoos/inmunología , Subgrupos de Linfocitos T/inmunología , Vacunas de Productos Inactivados
14.
Arch. méd. Camaguey ; 15(4)oct. 2010. graf
Artículo en Español | LILACS | ID: lil-615948

RESUMEN

La rinitis alérgica produce un importante deterioro de la calidad de vida. La inmunoterapia sublingual, representa una vía natural para la inducción de la tolerancia en este desorden alérgico. Objetivo: evaluar la eficacia y seguridad del extracto alergénico VALERGEN-DP del ácaro Dermatophagoides pteronyssinus como vacuna terapéutica sublingual en pacientes con rinitis alérgica. Método: ensayo clínico, fase II, a doble ciegas, paralelo, aleatorizado, controlado con un grupo placebo. Las vacunas se suministraron por vía sublingual en un esquema de incremento de dosis. El tratamiento tuvo una duración mínima de un año con evaluaciones frecuentes. Los 40 pacientes incluidos se asignaron a los dos grupos de forma pareja, 20 a cada uno, previo consentimiento informado. Resultados: se observó una disminución promedio en la media de los síntomas, así como en el consumo de medicamentos en el grupo activo en relación al placebo, dado por 156,3(p=0,000) y 43,5 (p=0,000) respectivamente. Los valores de la media de la reactividad cutánea descendieron en el grupo activo no así en el placebo en 2,6 %. Se reportaron solo cuatro eventos adversos, ninguno fatal, que representaron un 0,2 %. Conclusiones: la inmunoterapia sublingual con Dermatophagoide pteronyssinus es eficaz y segura para el tratamiento de los pacientes con rinitis alérgica.


Allergic rhinitis produced a significant deterioration in the quality of life. Sublingual immunotherapy represents a natural way to induce tolerance in the allergic disorder. Objective: to assess the efficacy and safety of allergenic extract VALERGEN-DP from mite Dermatophagoides pteronyssinus as sublingual therapeutic vaccine in patients with allergic rhinitis. Method: a clinical trial, phase II, double-blind, parallel, randomized, controlled with a placebo group was conducted. Vaccines were provided via sublingual in an increasing dose schedule. The treatment had a minimal duration of one year with frequent evaluations. The 40 patients included, two groups of 20 were assigned, previous informed consent. Results: it was observed an average decrease in the mean of symptoms, as well as drugs consumption in the active group in relation to the placebo with 156,3 (p=0,000) and 43.5 (p = 0, 000) respectively. Values of the mean of skin reactivity declined in the active group not so in the placebo with 2.6 %. Only four adverse events were reported, none fatal, representing a 0.2 %. Conclusions: sublingual immunotherapy with Dermatophagoide pteronyssinus is safe and effective for the treatment of patients with allergic rhinitis.


Asunto(s)
Humanos , Administración Sublingual , Ensayos Clínicos Fase II como Asunto , Dermatophagoides pteronyssinus , Inmunoterapia Activa , Rinitis
16.
Rev. medica electron ; 33(2)mar.-abr. 2011. tab
Artículo en Español | LILACS | ID: lil-616159

RESUMEN

La infección cutánea por Staphylococcus aureus constituye en estos momentos un problema de salud en nuestra población, por su elevada frecuencia, resistencia a la terapia antibiótica y por sus complicaciones. Se realizó un ensayo clínico, fase II, controlado, abierto y aleatorizado, con el objetivo de demostrar el efecto terapéutico y seguridad de la autovacuna como tratamiento de la estafilococia. Se incluyeron 457 pacientes con diagnóstico de Staphylococcus aureus en lesiones de piel, y se dividieron en dos grupos. El grupo A (237 pacientes), recibió la aplicación de la autovacuna obtenida a partir del microorganismo aislado en cada sujeto, y el grupo B (220 pacientes), recibió tratamiento antibiótico según resultados del antibiograma. Con la aplicación de la autovacuna, se obtuvo un 82 por ciento de curación, y sólo el 10 por ciento de los pacientes tuvo reaparición de forúnculos en el intervalo de 6 meses posterior a la terminación del tratamiento. Sin embargo, con la aplicación de la antibioticoterapia se observó un 12 por ciento de curación y un 75 por ciento de reaparición de forúnculos en ese intervalo de tiempo. La autovacuna resultó ser más eficaz en el tratamiento de la infección bacteriana por Staphylococcus aureus que los antimicrobianos, además de ser una inmunoterapia bien tolerada por la mayoría de los paciente


The skin infection by Staphylococcus aureus is currently a health problem in our population, because of its high frequency, resistance to the antibiotic therapy and its complications. We carried out a randomized, open, controlled, phase II clinical trial, with the objective of demonstrating the therapeutic effect and safety of the autovaccine as a treatment of the Staphylococcus infections. 457 patients with a diagnosis of Staphylococcus aureus in skin lesions were included, and they were divided in two groups. Group A (237 patients), received the autovaccine obtained form the micro organism isolated in each subject, and group B (220 patients), received antibiotic treatment according to the antibiogram results. With the application of the autovaccine, we obtained 82 per cent of healing, and only 10 per cent of the patients had the reappearance of furuncles in an interval of 6 months after finishing the treatment. However, with the application of the antibiotic therapy there was 12 per cent of healing and 75 per cent of reappearance of the furuncles in the mentioned time interval. The autovaccine was more effective in the treatment of the bacterial infection by Staphylococcus aureus that the antimicrobial agents besides being a good tolerated immunotherapy for most of the patients


Asunto(s)
Humanos , Adulto , Infecciones Cutáneas Estafilocócicas/terapia , Inmunoterapia Activa/métodos , Staphylococcus aureus/inmunología , Vacunas Bacterianas , Resultado del Tratamiento
17.
Chinese Journal of Contemporary Pediatrics ; (12): 149-152, 2011.
Artículo en Chino | WPRIM | ID: wpr-308851

RESUMEN

<p><b>OBJECTIVE</b>Some research has shown that Newcastle disease virus (NDV) is effective in the treatment of various tumors, including transferred melanoma and well differentiated renal cell carcinoma. This study aimed to evaluate the effect of NDV against human acute monocytic leukemia SHI-1 cells in vitro and in vivo.</p><p><b>METHODS</b>In vitro, the density and morphologic changes between wild SHI-1 cells (control) and NDV-infected SHI-1 cells were observed. MTT assay was utilized to observe the effect of NDV on the proliferation of SHI-1 cells. In vivo, the effect of NDV on the tumor inhibition was assessed using SHI-1 xenografts subcutaneously established in CD-1 nude mice. NDV was given by intra-tumor injections, and the tumor inhibition rate and toxic effects were evaluated.</p><p><b>RESULTS</b>In the control group, the SHI-1 cells were observed using an inverted microscope to be regular in morphology and intensive in distribution. In the NDV-infected group, the SHI-1 cells were irregular and sparsate, and the aggregate and fused cells were common. MTT assay showed that the proliferation of SHI-1 cells were significantly inhibited by NDV at different concentrations (P<0.01) and in a time- and concentration-dependent manner. The tumor inhibition rate in the NDV group was 84.7%, which was significantly higher than that in the control group (P<0.01). No toxic effects were observed in the nude mice.</p><p><b>CONCLUSIONS</b>NDV can suppress the proliferation of human acute monocytic leukemic cells both in vitro and in vivo. The safety of NDV is reliable.</p>


Asunto(s)
Animales , Humanos , Ratones , Proliferación Celular , Inmunoterapia Activa , Leucemia Monocítica Aguda , Terapéutica , Ratones Desnudos , Virus de la Enfermedad de Newcastle , Fisiología , Ensayos Antitumor por Modelo de Xenoinjerto
18.
Chinese Journal of Otorhinolaryngology Head and Neck Surgery ; (12): 36-39, 2011.
Artículo en Chino | WPRIM | ID: wpr-277509

RESUMEN

<p><b>OBJECTIVE</b>To evaluate the efficacy and immunological changes of children receiving subcutaneous immunotherapy with Dermatophagoides pteronyssinus.</p><p><b>METHODS</b>Sixty-four children with allergic rhinitis to Dermatophagoides pteronyssinus (Der p) were randomly allocated to receive either specific immunotherapy (n = 32) or medical treatment (n = 32). Symptom and medication scores were assessed to evaluate the clinical efficacy in the baseline and after one year treatment. Total IgE, Der p-specific IgE, and specific IgG4 were measured.</p><p><b>RESULTS</b>Immunotherapy reduced the symptom (the scores reduced from 10[9;11] to 4[3;6]) and medication score (the scores reduced from 0.76[0.61;0.90] to 0.35[0.30;0.43]) in children with allergic rhinitis significantly(Z value were -4.80 and -4.74, respectively, each P < 0.01). There was a significant difference in symptom and medication scores between both groups after one year treatment (U value were 155.00 and 139.50, respectively, each P < 0.01). There were no differences in levels of serum total IgE, specific IgE before and after one year treatment, but the level of serum specific IgG4 increased significantly after one year treatment.</p><p><b>CONCLUSIONS</b>Immunotherapy with standardized extract is efficacious to treat children sensitive to Der p, allergen-specific IgG4 is significant as immunological marker to predict efficacy of immunotherapy.</p>


Asunto(s)
Adolescente , Animales , Niño , Femenino , Humanos , Masculino , Alérgenos , Alergia e Inmunología , Farmacología , Antígenos Dermatofagoides , Alergia e Inmunología , Farmacología , Desensibilización Inmunológica , Inmunoglobulina E , Sangre , Inmunoterapia Activa , Ácaros , Alergia e Inmunología , Rinitis Alérgica Perenne , Alergia e Inmunología , Terapéutica , Resultado del Tratamiento
19.
Acta méd. costarric ; 52(4): 192-194, dic. 2010.
Artículo en Español | LILACS | ID: lil-700606
20.
J. bras. med ; 98(4): 22-24, ago.-set. 2010. tab
Artículo en Portugués | LILACS | ID: lil-566751

RESUMEN

Objetivo: Avaliar a ação do ß-1-3 glucan na resposta imunológica de pacientes portadores de cáncer de intestino submetidos à cirurgia, quimioterapia e radioterapia. Método: Estudo retrospectivo de 75 pacientes, analisando as variações dos valores dos leucócitos, linfócitos e subpopulações CD4 e CD8 com o uso de ß-1-3 glucan. Resultados: Houve um aumento no número de todas as linhagens celulares estudadas, principalmente a da subpopulação de linfócitos CD4 (29,70%). A análise estatística pelo teste "t" de Student e pelo de Wilcoxon mostrou que os resultados foram significativos. Conclusão: O uso do ß-1-3 glucan foi capaz de restaurar e manter a resposta imune, reduzir os danos imunossupressores da quimioterapia e radioterapia e o seu uso não demonstrou efeitos colaterais.


Objective: To review the effectiveness of ß-1-3 glucan in the immune response of patients with intestinal cancer submitted to surgery, chemo and radiotherapy. Methods: Retrospective study on 75 patients, analyzing the variations on the leucocytes, lymphocytes and CD4/CD8 lymphocyte subpopulations using ß-1-3 glucan. Results: There was an increase in the general cellular sample, especially on CD4 lymphocyte subpopulations. Statistica analyses via Student's t-test and the Wilcoxon test have showed that the resultshave been significant. Conclusion: The use of ß-1-3 glucan was able to restore and keep the immune response in check, and to reduce the immunosupressor damages from chemo and radiotherapy. There were no side effects.


Asunto(s)
Humanos , Masculino , Femenino , Neoplasias Intestinales/cirugía , Neoplasias Intestinales/tratamiento farmacológico , Neoplasias Intestinales/terapia , Radioterapia , Adyuvantes Inmunológicos/uso terapéutico , /uso terapéutico , Inmunoterapia Activa , Linfocitos T/inmunología , Saccharomyces cerevisiae
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