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1.
J Comput Assist Tomogr ; 41(3): 484-488, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-27798445

RESUMEN

BACKGROUND AND PURPOSE: Dental and periodontal diseases represent important but often overlooked causes of acute sinusitis. Our goal was to examine the prevalence of potential odontogenic sources of acute maxillary sinusitis according to immune status and their associations with sinusitis. MATERIALS AND METHODS: A retrospective review of maxillofacial computed tomography studies from 2013 to 2014 was performed. Each maxillary sinus and its ipsilateral dentition were evaluated for findings of acute sinusitis and dental/periodontal disease. RESULTS: Eighty-four patients (24 immunocompetent, 60 immunocompromised) had 171 maxillary sinuses that met inclusion criteria for acute maxillary sinusitis. Inspection of dentition revealed oroantral fistula in 1%, periapical lucencies in 16%, and projecting tooth root(s) in 71% of cases. Immunocompromised patients were more likely to have bilateral sinusitis than immunocompetent patients (67% vs 33%, P = 0.005). A paired case-control analysis in a subset of patients with unilateral maxillary sinusitis (n = 39) showed a higher prevalence of periapical lucency in association with sinuses that had an air fluid level-29% of sinuses with a fluid level had periapical lucency compared with 12% without sinus fluid (P = 0.033). CONCLUSIONS: Potential odontogenic sources of acute maxillary sinusitis are highly prevalent in both immunocompetent and immunocompromised patients, although the 2 patient populations demonstrate no difference in the prevalence of these potential odontogenic sources. Periapical lucencies were found to be associated with an ipsilateral sinus fluid level. Increased awareness of the importance of dental and periodontal diseases as key components of maxillofacial computed tomography interpretation would facilitate a more appropriate and timely treatment.


Asunto(s)
Inmunocompetencia/inmunología , Huésped Inmunocomprometido/inmunología , Sinusitis Maxilar/diagnóstico por imagen , Enfermedades Periodontales/diagnóstico por imagen , Análisis de Causa Raíz/métodos , Tomografía Computarizada por Rayos X , Enfermedades Dentales/diagnóstico por imagen , Enfermedad Aguda , Huesos Faciales/diagnóstico por imagen , Humanos , Maxilar/diagnóstico por imagen , Sinusitis Maxilar/complicaciones , Sinusitis Maxilar/inmunología , Enfermedades Periodontales/complicaciones , Enfermedades Periodontales/inmunología , Estudios Retrospectivos , Enfermedades Dentales/complicaciones , Enfermedades Dentales/inmunología
2.
Ann Rheum Dis ; 73(12): 2094-100, 2014 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-23918037

RESUMEN

OBJECTIVES: To examine the safety and efficacy of 5-year administration of certolizumab pegol (CZP)+methotrexate (MTX) in patients with active rheumatoid arthritis (RA). METHODS: Eligible patients from the Rheumatoid Arthritis Prevention of Structural Damage (RAPID)1 randomised controlled trial (RCT) were treated in open-label extension (OLE) with CZP 400 mg every other week (Q2W), reduced to 200 mg Q2W after ≥6 months, +MTX. Combined safety data from RCT and OLE are presented from initiation of CZP treatment to 12 wks post last visit in patients receiving ≥1 dose of CZP (Safety population, N=958). Efficacy data are presented to start of first site closure (wk 256 of CZP treatment: 52 wks in RCT+204 wks in OLE) for all patients randomised to receive CZP (intent-to-treat (ITT) population, N=783) and CZP patients who completed the 52 wk RCT and enrolled into OLE (wk 52 CZP completers, N=508). Disease Activity Score (DAS)28 (Erythrocyte Sedimentation Rate (ESR)), American College of Rheumatology Criteria (ACR) 20/50/70, Health Assessment Questionnaire - Disability Index (HAQ-DI), and patient retention (Kaplan-Meier analysis) were assessed. RESULTS: Overall event rate per 100 patient-years (ER) of adverse events (AEs) was 290.4, most frequently: urinary tract infections (ER=7.9), nasopharyngitis (ER=7.3) and upper respiratory tract infections (ER=7.3). ER of serious AEs was 20.3 (infections=5.9, malignancies=1.2). 21 patients (2.2%) experienced an AE resulting in death (incidence rate=0.6). At wk 256 of treatment, 55.3% of the CZP ITT population were estimated to remain on treatment (68.7% if solely withdrawals due to AE or lack of efficacy were considered). In wk 52 CZP completers and CZP ITT population, DAS28 (ESR) remission rates and improvements from baseline were sustained to wk 256. CONCLUSIONS: CZP+MTX treatment provided a favourable risk-benefit profile over 5 years in patients with active RA. No new safety signals were identified.


Asunto(s)
Anticuerpos Monoclonales Humanizados/uso terapéutico , Artritis Reumatoide/tratamiento farmacológico , Fragmentos Fab de Inmunoglobulinas/uso terapéutico , Inmunosupresores/uso terapéutico , Metotrexato/uso terapéutico , Polietilenglicoles/uso terapéutico , Adulto , Certolizumab Pegol , Estudios de Cohortes , Quimioterapia Combinada , Femenino , Humanos , Huésped Inmunocomprometido/inmunología , Estudios Longitudinales , Masculino , Persona de Mediana Edad , Faringitis/inmunología , Infecciones del Sistema Respiratorio/inmunología , Resultado del Tratamiento , Infecciones Urinarias/inmunología
3.
Rheumatol Int ; 30(3): 405-8, 2010 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-19449010

RESUMEN

We report a case of sudden onset of late infection after TKA inflamed by anti-TNFalpha therapy, Infliximab, in a 54-year-old woman with RA. Infliximab therapy was started 3 years and 8 months after TKAs as a result of multiple arthritides showing high inflammation of RA. One week after the third administration of Infliximab, the patient suffered sudden knee pain and infectious clinical symptoms, and bacteria (MSSA) were detected by joint effusion culture. She was successfully treated by open debridement with antibiotics-loaded calcium phosphate bone paste and cement and the prostheses were retained. Early diagnosis and operative treatment might be the key to controlling infected TKA without removing the implant. This present case might indicate a serious risk of immunosuppressive effects caused by Infliximab.


Asunto(s)
Anticuerpos Monoclonales/efectos adversos , Artritis Reumatoide/cirugía , Artroplastia de Reemplazo de Rodilla/efectos adversos , Articulación de la Rodilla/fisiopatología , Infecciones Relacionadas con Prótesis/inducido químicamente , Infección de la Herida Quirúrgica/inducido químicamente , Antibacterianos/uso terapéutico , Antirreumáticos/efectos adversos , Artritis Reumatoide/inmunología , Artritis Reumatoide/fisiopatología , Cementos para Huesos/uso terapéutico , Diagnóstico Precoz , Femenino , Humanos , Enfermedad Iatrogénica/prevención & control , Huésped Inmunocomprometido/efectos de los fármacos , Huésped Inmunocomprometido/inmunología , Terapia de Inmunosupresión/efectos adversos , Infliximab , Articulación de la Rodilla/inmunología , Articulación de la Rodilla/microbiología , Persona de Mediana Edad , Implantación de Prótesis/efectos adversos , Infecciones Relacionadas con Prótesis/inmunología , Infecciones Relacionadas con Prótesis/microbiología , Infección de la Herida Quirúrgica/inmunología , Infección de la Herida Quirúrgica/microbiología , Factores de Tiempo , Factor de Necrosis Tumoral alfa/antagonistas & inhibidores
4.
Braz Oral Res ; 34: e048, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32428085

RESUMEN

In less than four months, an unprecedented pandemic changed the world scenario, closing institutions and commerce, paralyzing sports championships, blocking frontiers, and putting almost all populations in a house quarantine regimen. Immunocompromised patients are within the high-risk group to severe outcomes from COVID-19. However, there is no clear evidence of the association between impaired immune host status and complications from SARS-CoV-2 infection so far. The virus is transmitted by inhalation or direct contact with infected secretions, and therefore the dental office is a highly susceptible environment for such transmission. Here, we review the literature and discuss immunological COVID-19 related issues. We also make suggestions for immunocompromised patients' support in this new emerging context of clinical dental practice. Until comprehensive findings are published, individuals with impaired immunity should be considered as high-risk. Cross infection control procedures for the clinical care of immunocompromised patients should follow the same guidelines that are being proposed for immunocompetent ones. However, during the active outbreak, people under immunosuppressive conditions should not receive elective procedures, even if they do not have symptoms or exposure history to COVID-19, and in case of emergence, care must be done in a separate airborne room. In the pos-pandemic phase, the dental care general recommendations should be the same for all subjects. Changes in the current guidelines have been proposed to SARS-CoV-2 infection control in order to provide the best and safe dental practice. However, they still need to be validated by future studies.


Asunto(s)
Betacoronavirus , Infecciones por Coronavirus/inmunología , Atención Odontológica/normas , Huésped Inmunocomprometido/inmunología , Neumonía Viral/inmunología , Microbiología del Aire/normas , COVID-19 , Infecciones por Coronavirus/transmisión , Infecciones por Coronavirus/virología , Consultorios Odontológicos , Humanos , Pandemias , Neumonía Viral/transmisión , Neumonía Viral/virología , SARS-CoV-2
5.
Asian J Androl ; 22(1): 28-33, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-31489848

RESUMEN

Inflatable penile prostheses are an important tool in the treatment of medically refractory erectile dysfunction. One of the major complications associated with these prostheses is infections, which ultimately require device explanation and placement of a new device. Over the past several decades, significant work has been done to reduce infection rates and optimize treatment strategies to reduce patient morbidity. This article reviews the current state of knowledge surrounding penile prosthesis infections, with attention to the evidence for methods to prevent infection and best practices for device reimplantation.


Asunto(s)
Disfunción Eréctil/cirugía , Implantación de Pene/métodos , Prótesis de Pene , Infecciones Relacionadas con Prótesis/prevención & control , Infección de la Herida Quirúrgica/prevención & control , Antibacterianos/uso terapéutico , Antiinfecciosos Locales/uso terapéutico , Profilaxis Antibiótica/métodos , Vendajes , Portador Sano/diagnóstico , Portador Sano/tratamiento farmacológico , Clorhexidina/uso terapéutico , Materiales Biocompatibles Revestidos , Remoción de Dispositivos , Diabetes Mellitus/epidemiología , Disfunción Eréctil/epidemiología , Infecciones por Bacterias Gramnegativas/epidemiología , Infecciones por Bacterias Gramnegativas/inmunología , Infecciones por Bacterias Gramnegativas/prevención & control , Infecciones por Bacterias Gramnegativas/terapia , Remoción del Cabello/métodos , Humanos , Huésped Inmunocomprometido/inmunología , Masculino , Cuidados Preoperatorios/métodos , Infecciones Relacionadas con Prótesis/epidemiología , Infecciones Relacionadas con Prótesis/inmunología , Infecciones Relacionadas con Prótesis/terapia , Reoperación , Factores de Riesgo , Traumatismos de la Médula Espinal/epidemiología , Infecciones Estafilocócicas/epidemiología , Infecciones Estafilocócicas/inmunología , Infecciones Estafilocócicas/prevención & control , Infecciones Estafilocócicas/terapia , Staphylococcus aureus , Staphylococcus epidermidis , Paños Quirúrgicos , Instrumentos Quirúrgicos , Infección de la Herida Quirúrgica/epidemiología , Infección de la Herida Quirúrgica/inmunología , Infección de la Herida Quirúrgica/terapia
6.
Aliment Pharmacol Ther ; 28(6): 742-8, 2008 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-19145730

RESUMEN

BACKGROUND: Efficacy and safety of antiviral combination therapy in patients with Crohn's disease (CD) and chronic hepatitis C (CHC) is presently not established and consequently CHC is rarely treated in CD patients. AIM: To analyse the efficacy and tolerability of antiviral interferon/ribavirin therapy in patients with CHC and CD. METHODS: Eleven HCV-infected CD patients received either 3 x 1.5 microg/kg/week interferon-alpha-2b or 180 microg/week peginterferon-alpha-2a (PEGASYS; Roche, Basel, Switzerland) as monotherapy (n = 1) or in combination with 800-1200 mg/day ribavirin (COPEGUS; Roche) (n = 10) for 24-54 weeks according to HCV-genotype and initial response respectively. Eight patients were under CD-specific therapy. RESULTS: Five (46%) patients (HCV-1: a = 3; HCV-2: n = 0; HCV-3: n = 1; unknown: n = 1) achieved a sustained virological response, three (27%) patients relapsed, three (27%) were nonresponders (all GT 1b). At baseline, the Harvey--Bradshaw Index was 0 (0-8) [median (range)], increased on antiviral therapy to 4 (1-15) (P = 0.005) and decreased to baseline level 0 (0-6) after 6-month follow-up. CONCLUSIONS: This preliminary experience demonstrates that treatment of CHC in patients with CD is comparable to the treatment of CHC in those without CD. However, gastrointestinal symptoms may be temporarily exacerbated and haemopoietic growth factors may be required.


Asunto(s)
Antivirales/uso terapéutico , Enfermedad de Crohn/tratamiento farmacológico , Hepatitis C Crónica/tratamiento farmacológico , Huésped Inmunocomprometido/inmunología , Interferón-alfa/uso terapéutico , Polietilenglicoles/uso terapéutico , Adulto , Comorbilidad , Enfermedad de Crohn/epidemiología , Enfermedad de Crohn/inmunología , Quimioterapia Combinada , Femenino , Hepacivirus/aislamiento & purificación , Hepatitis C Crónica/epidemiología , Hepatitis C Crónica/inmunología , Humanos , Inmunosupresores/uso terapéutico , Interferón alfa-2 , Recuento de Leucocitos , Masculino , Persona de Mediana Edad , Reacción en Cadena de la Polimerasa , ARN Viral/sangre , Proteínas Recombinantes , Estudios Retrospectivos , Ribavirina/uso terapéutico , Resultado del Tratamiento
7.
J Oral Maxillofac Surg ; 66(3): 475-85, 2008 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-18280380

RESUMEN

PURPOSE: This retrospective study describes the clinical features and management of noma (cancrum oris) in patients with HIV and AIDS. PATIENTS AND METHODS: Records of 48 consecutive patients with noma (cancrum oris) seen between July 2002 and November 2006 were reviewed for age, gender, clinical features, and management. Other reports on noma in HIV and AIDS in Zimbabwe were also reviewed. RESULTS: There were 48 patients included; 35.4% (n = 17) were males, of which 64.7% (n = 11) were children (16 years and younger) and 35.3% (n = 6) were adults; 64.6% (n = 31) were females, out of which 87.1% (n = 27) were children and 12.9% (n = 4) were adults. The average age was 14.2 years (range, 3 to 30 years) for males and 9.2 years (range, 1 to 36 years) for females. The average age for the entire group was 11 years (range, 1 to 36 years). All patients were HIV-positive by the ELISA method. Only 13 patients had CD4 cell and CD8 cell count obtained, ranging from 10 to 594 cells/microL with a CD4/CD8 ratio ranging from 0.02 to 0.45. Only 5 patients had microbiologic investigations conducted, isolating Staphylococcus aureus, Klebsiella species, group D Streptococcus, and group B hemolytic Streptococcus. Isolated cheek defect (37.5%) was most common, followed by the type I and type IV defect (25% each). Administration of antibiotics, nutritional support, wound debridement, and sequestrectomy were conducted before definitive reconstructive surgery. Facial reconstruction was performed using distant and local advancement flaps. No bony reconstruction was performed. Satisfactory results were achieved with minimal infection and flap breakdown. Follow-up was difficult; patients were lost to follow-up within 6 to 12 months after surgery. CONCLUSION: Noma cases are on the increase in line with the current HIV and AIDS epidemic. Female children appear to be more commonly affected than their male counterparts. Reconstructive surgery is possible in patients with low CD4/CD8 ratios because of HIV infection.


Asunto(s)
Infecciones por VIH/complicaciones , Huésped Inmunocomprometido/inmunología , Noma/terapia , Procedimientos Quirúrgicos Orales/métodos , Procedimientos de Cirugía Plástica/métodos , Síndrome de Inmunodeficiencia Adquirida/complicaciones , Adolescente , Adulto , Antígenos CD4/análisis , Recuento de Linfocito CD4 , Relación CD4-CD8 , Antígenos CD8/análisis , Niño , Preescolar , Femenino , Humanos , Masculino , Noma/inmunología , Noma/microbiología , Terapia Nutricional , Estudios Retrospectivos , Factores Sexuales , Zimbabwe
8.
J Int Acad Periodontol ; 10(1): 10-5, 2008 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-18333595

RESUMEN

Necrotizing gingivitis (NG) is a well-known periodontal condition characterized by marginal gingival necrosis, bleeding and pain. Necrotizing periodontitis is an extension of NG into the periodontal attachment apparatus, and the two stages are referred to collectively as necrotizing periodontal diseases (NPD). Necrotizing periodontal diseases in HIV-seropositive subjects are similar with regard to the spectrum of periodontopathic bacteria, the clinical manifestations, the natural course and the response to treatment when compared to NPD in HIV-seronegative subjects. However, in the former group, there is an increase in the prevalence of candidal species and herpesviruses in the subgingival plaque and gingival biopsy specimens. In the periodontal tissues, spirochaetes, activated herpesviruses, Candida species and HIV have the capability of deregulating host innate and adaptive immune responses and of stimulating host inflammatory reactions, and may therefore explain the greater prevalence of NPD in HIV-seropositive subjects compared to immunocompetent subjects.


Asunto(s)
Gingivitis Ulcerosa Necrotizante/microbiología , Seropositividad para VIH/complicaciones , Periodontitis/microbiología , Antiinfecciosos/uso terapéutico , Candida albicans/patogenicidad , Clorhexidina/uso terapéutico , Citocinas/fisiología , Raspado Dental , Gingivitis Ulcerosa Necrotizante/complicaciones , Gingivitis Ulcerosa Necrotizante/inmunología , Gingivitis Ulcerosa Necrotizante/terapia , Seropositividad para VIH/inmunología , Herpesviridae/patogenicidad , Humanos , Huésped Inmunocomprometido/inmunología , Metronidazol/uso terapéutico , Periodontitis/complicaciones , Periodontitis/inmunología , Periodontitis/terapia , Spirochaetales/patogenicidad , Linfocitos T/fisiología
10.
Braz. oral res. (Online) ; 34: e048, 2020.
Artículo en Inglés | LILACS, BBO - odontología (Brasil) | ID: biblio-1132664

RESUMEN

Abstract In less than four months, an unprecedented pandemic changed the world scenario, closing institutions and commerce, paralyzing sports championships, blocking frontiers, and putting almost all populations in a house quarantine regimen. Immunocompromised patients are within the high-risk group to severe outcomes from COVID-19. However, there is no clear evidence of the association between impaired immune host status and complications from SARS-CoV-2 infection so far. The virus is transmitted by inhalation or direct contact with infected secretions, and therefore the dental office is a highly susceptible environment for such transmission. Here, we review the literature and discuss immunological COVID-19 related issues. We also make suggestions for immunocompromised patients' support in this new emerging context of clinical dental practice. Until comprehensive findings are published, individuals with impaired immunity should be considered as high-risk. Cross infection control procedures for the clinical care of immunocompromised patients should follow the same guidelines that are being proposed for immunocompetent ones. However, during the active outbreak, people under immunosuppressive conditions should not receive elective procedures, even if they do not have symptoms or exposure history to COVID-19, and in case of emergence, care must be done in a separate airborne room. In the pos-pandemic phase, the dental care general recommendations should be the same for all subjects. Changes in the current guidelines have been proposed to SARS-CoV-2 infection control in order to provide the best and safe dental practice. However, they still need to be validated by future studies.


Asunto(s)
Humanos , Neumonía Viral/inmunología , Atención Odontológica/normas , Huésped Inmunocomprometido/inmunología , Infecciones por Coronavirus/inmunología , Betacoronavirus , Neumonía Viral/transmisión , Neumonía Viral/virología , Infecciones por Coronavirus/transmisión , Infecciones por Coronavirus/virología , Consultorios Odontológicos , Microbiología del Aire/normas , Pandemias , SARS-CoV-2 , COVID-19
12.
Dent Clin North Am ; 47(4): 641-64, v-vi, 2003 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-14664457

RESUMEN

Two very successful approaches aimed at preventing infectious diseases acquired in the dental office have introduced more vigilant infection control and barrier techniques as well as the use of specific immunizations. Special consideration is given to the subgroup of dental professionals at increased risk for common diseases that may prevail because of the location and demographics of their practices. A brief review of the basic principles of immunology and immunization is covered as well as immunizations and the medically compromised oral health care worker, the medically compromised patient, new vaccines that may be in the offing, and the future role of immunization for dentists.


Asunto(s)
Control de Enfermedades Transmisibles/normas , Infección Hospitalaria/prevención & control , Auxiliares Dentales , Odontólogos , Inmunización/normas , Enfermedades Profesionales/prevención & control , Contraindicaciones , Atención Dental para Enfermos Crónicos , Humanos , Inmunización/efectos adversos , Esquemas de Inmunización , Huésped Inmunocomprometido/inmunología , Control de Infecciones/normas , Transmisión de Enfermedad Infecciosa de Paciente a Profesional/prevención & control , Transmisión de Enfermedad Infecciosa de Profesional a Paciente/prevención & control , Vacunación/efectos adversos , Vacunación/normas
14.
Arch Inst Pasteur Tunis ; 77(1-4): 51-4, 2000.
Artículo en Francés | MEDLINE | ID: mdl-14658228

RESUMEN

The immunodepression, related or not to AIDS, induces the emergence of opportunistic parasitosis and mycosis. Our objective is to analyze these pathogenic agents, their clinical expression and gravity in immunocompromised individuals. Our retrospective 9 years study reported parasitic and fungic infections complicating immunodepression. Among 31 HIV infected patients, we diagnosed the following parasitosis: Cryptosporidium (7 cases), Isospora belli (2 cases) and Enterocytozoon bieneusi (1 case). Pulmonary pneumocystosis was diagnosed in 6 cases, cerebral toxoplasmosis in 6 cases and meningo-cerebral cryptococcosis in 1 case. The systemic candidasis was diagnosed in 13 leukaemic patients. The intestinal anguilluliasis was found in 5 patients treated with corticoïds for long periods. A case of Kala azar was observed in a 83 years man treated with corticoïds. A disseminated aspergillosis occurred in a child with a Chediack Higashi syndrome. A gingivo-labial fusariosis was diagnosed in a leukaemic patient. This emergency of the new parasitic and fungal agents requires a better understanding of these affections in order to improve their early diagnosis and treatments.


Asunto(s)
Infecciones Oportunistas Relacionadas con el SIDA/epidemiología , Huésped Inmunocomprometido , Micosis/epidemiología , Enfermedades Parasitarias/epidemiología , Infecciones Oportunistas Relacionadas con el SIDA/diagnóstico , Infecciones Oportunistas Relacionadas con el SIDA/inmunología , Infecciones Oportunistas Relacionadas con el SIDA/parasitología , Centros Médicos Académicos , Aspergilosis/epidemiología , Candidiasis/epidemiología , Criptosporidiosis/epidemiología , Enterocytozoon , Humanos , Huésped Inmunocomprometido/inmunología , Isosporiasis/epidemiología , Leishmaniasis Visceral/epidemiología , Microsporidiosis/epidemiología , Micosis/diagnóstico , Micosis/inmunología , Micosis/microbiología , Enfermedades Parasitarias/diagnóstico , Enfermedades Parasitarias/inmunología , Enfermedades Parasitarias/parasitología , Neumonía por Pneumocystis/epidemiología , Vigilancia de la Población , Estudios Retrospectivos , Estrongiloidiasis/epidemiología , Toxoplasmosis Cerebral/epidemiología , Túnez/epidemiología
15.
J Med Case Rep ; 8: 463, 2014 Dec 25.
Artículo en Inglés | MEDLINE | ID: mdl-25539638

RESUMEN

INTRODUCTION: Mycobacterium europaeum, a slow-growing nontuberculous mycobacteria belonging to the Mycobacterium simiae complex, was described after the seminal characterization of five isolates collected from three sputum specimens and a jaw gland biopsy in Italy, Greece and Sweden. Five respiratory tract isolates were further reported in Iran. Here, we report the first isolation of M. europaeum in France, in the respiratory tract of a patient co-infected with human immunodeficiency virus and hepatitis C virus. CASE PRESENTATION: A 49-year-old Caucasian woman with a 26-year history of human immunodeficiency virus-hepatitis C virus co-infection was admitted for significant influenza-like syndrome in a context of repetitive exacerbations of chronic obstructive pulmonary disease. Significant biological parameters included lymphocytes of 1.6G/L including 237/mm3 T4 lymphocytes, a human immunodeficiency virus viral load of 1.6 log and a hepatitis C virus viral load of 6 log. Reverse-transcriptase polymerase chain reaction of her nasopharyngeal aspiration confirmed influenza A H1N1. Three sputum specimens lacked acid-fast bacilli but one grew mycobacteria identified by using matrix-assisted laser desorption ionization/time-of-flight mass spectrometry as M. europaeum with a 1.56 log score. A 1,482-bp 16S ribosomal ribonucleic acid gene sequence yielded 99% similarity with both Mycobacterium parascrofulaceum ATCC BAA-614 and M. europaeum DSM 45397T and partial rpoB polymerase chain reaction-sequencing yielded a 725-bp sequence exhibiting 100% similarity with M. europaeum strain DSM 45397T. CONCLUSIONS: We report the first isolation of M. europaeum in France, in the respiratory tract of a patient co-infected with human immunodeficiency virus and hepatitis C virus. M. europaeum warrants further attention in immunosuppressed patients with influenza, using matrix-assisted laser desorption ionization/time-of-flight mass spectrometry and rpoB partial sequencing as tools for its accurate identification.


Asunto(s)
Huésped Inmunocomprometido/inmunología , Subtipo H1N1 del Virus de la Influenza A , Gripe Humana/diagnóstico , Mycobacterium/aislamiento & purificación , Sistema Respiratorio/microbiología , Coinfección , Femenino , Francia , Infecciones por VIH/complicaciones , Infecciones por VIH/inmunología , Hepatitis C/complicaciones , Hepatitis C/inmunología , Humanos , Gripe Humana/complicaciones , Gripe Humana/inmunología , Espectrometría de Masas , Persona de Mediana Edad , Sistema Respiratorio/inmunología , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Esputo/microbiología
16.
J Periodontol ; 82(2): 251-8, 2011 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-20722530

RESUMEN

BACKGROUND: The aim of this study is to make a longitudinal evaluation of the incidence and severity of gingival overgrowth (GO) induced by immunosuppressive agents, such as tacrolimus (Tcr) and cyclosporin A (CsA), in the absence of calcium channel blockers in patients undergoing renal transplantation (RT). METHODS: This longitudinal study is conducted in 49 patients with RT who were divided into a CsA group (n = 25) and Tcr group (n = 24). The individuals were assessed at four time intervals: before transplant and 30, 90, and 180 days after RTs. Demographic data and periodontal clinical parameters (plaque index, cemento-enamel junction to the gingival margin, probing depth, clinical attachment level, bleeding on probing [BOP], and GO) were collected at all time intervals. RESULTS: The mean GO index was significantly lower in the Tcr group compared to the CsA group after 30 (P = 0.03), 90 (P = 0.004), and 180 (P = 0.01) days of immunosuppressive therapy. One hundred eighty days after RTs, a clinically significant GO was observed in 20.0% of individuals in the CsA group and 8.3% of individuals in the Tcr group. However, this difference was not statistically significant (P = 0.41). There was a reduction in periodontal clinical parameters regarding the time of immunosuppressive therapy for PI and BOP (P <0.001) in both groups. CONCLUSION: Although there was no statistical difference in the incidences of clinically significant GO after 180 days of immunosuppressive therapy, it was observed that GO occurred later in the Tcr group, and the severity of GO in this group was lower than in patients who used CsA.


Asunto(s)
Ciclosporina/efectos adversos , Sobrecrecimiento Gingival/inducido químicamente , Inmunosupresores/efectos adversos , Trasplante de Riñón/inmunología , Tacrolimus/efectos adversos , Adulto , Análisis de Varianza , Bloqueadores de los Canales de Calcio/uso terapéutico , Femenino , Sobrecrecimiento Gingival/inmunología , Humanos , Huésped Inmunocomprometido/efectos de los fármacos , Huésped Inmunocomprometido/inmunología , Terapia de Inmunosupresión/métodos , Estudios Longitudinales , Masculino , Persona de Mediana Edad , Índice de Severidad de la Enfermedad , Estadísticas no Paramétricas , Adulto Joven
18.
Nan Fang Yi Ke Da Xue Xue Bao ; 28(10): 1911-3, 2008 Oct.
Artículo en Zh | MEDLINE | ID: mdl-18971199

RESUMEN

OBJECTIVE: To observe the effects of bagasse polysaccharide on the immune functions of immunosuppressed mice. METHODS: Immunosuppressed mouse models were established by intraperitoneal injections with cyclophosphamide followed by daily intragastric administration of bagasse polysaccharide. After the treatments, the mice were examined for immune organ weight index, phagocytotic function of the macrophages, delayed type hypersensitivity, serum IgM level following exposure to chicken red blood cells, formation of hemolytic plaques, T cell percentage and lymphocyte transformation. RESULTS: Treatment of the immunosuppressed mice with bagasse polysaccharide at the daily dose of 200 and 400 mg/kg significantly increased the weight of the immune organs, phagocytotic function of the macrophages, delayed type hypersensitivity, serum IgM level against chicken red blood cells, formation of hemolytic plaques, T cell percentage and lymphocyte transformation. CONCLUSION: Bagasse polysaccharide can enhance the immune functions of immunosuppressed mice.


Asunto(s)
Celulosa/química , Huésped Inmunocomprometido/inmunología , Activación de Linfocitos/efectos de los fármacos , Polisacáridos/farmacología , Animales , Ciclofosfamida , Femenino , Macrófagos/inmunología , Masculino , Ratones , Fagocitosis/efectos de los fármacos , Distribución Aleatoria
19.
Artículo en Inglés | MEDLINE | ID: mdl-18155610

RESUMEN

In 2001, the World Health Organization (WHO) published its new classification of tumors of hematopoietic and lymphoid tissues, including an entity named posttransplantation lymphoproliferative disorder (PTLD). Because oral PTLD is of clinical relevance to oral health providers, the importance of distinguishing between PTLD and nontransplantation related lymphoma is outlined, and the clinical implications of oral PTLD are discussed.


Asunto(s)
Enfermedades de las Encías/patología , Trasplante de Células Madre Hematopoyéticas/efectos adversos , Huésped Inmunocomprometido/inmunología , Trastornos Linfoproliferativos/patología , Resultado Fatal , Enfermedades de las Encías/terapia , Enfermedades de las Encías/virología , Herpesvirus Humano 4 , Humanos , Trastornos Linfoproliferativos/terapia , Trastornos Linfoproliferativos/virología , Masculino , Persona de Mediana Edad , Organización Mundial de la Salud
20.
Artículo en Inglés | MEDLINE | ID: mdl-18442743

RESUMEN

OBJECTIVE: The objective of this study was to assess if there is increased herpes simplex virus type 1 (HSV-1) salivary shedding in oncology pediatric patients with severe cytopenia (SC). STUDY DESIGN: HSV-1 was detected by real time PCR in saliva samples from oncology pediatric patients (n = 30) during SC and relative cytopenia (RC), and from healthy children (n = 27). RESULTS: The frequency of HSV-1 positive saliva samples was higher in patients with SC as compared to controls (P < .05), and this frequency presented a significant reduction during RC periods (P < .02). The SC group positive for HSV-1 presented both a twofold increase in the neutrophil-to-lymphocyte ratio as compared with SC patients negative for HSV-1 (P < .05), and a positive correlation between neutrophil and lymphocyte counts (P < .05, R = 0.82, R(2) = 0.67). This correlation was not found in oncology patients negative for HSV-1 during SC and RC. CONCLUSION: Severe cytopenia in oncology pediatric patients could be an important susceptibility factor for increased HSV-1 salivary shedding.


Asunto(s)
Herpesvirus Humano 1/fisiología , Huésped Inmunocomprometido/inmunología , Leucopenia/virología , Neoplasias/sangre , Saliva/virología , Antineoplásicos/efectos adversos , Estudios de Casos y Controles , Niño , Preescolar , ADN Viral/análisis , Herpesvirus Humano 1/aislamiento & purificación , Humanos , Lactante , Recuento de Leucocitos , Leucopenia/inducido químicamente , Neoplasias/tratamiento farmacológico , Reacción en Cadena de la Polimerasa , Estadísticas no Paramétricas , Esparcimiento de Virus
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