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1.
Int J Hematol ; 118(5): 652-655, 2023 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-37532827

RESUMO

Recommendations and guidelines for management of SARS-COV-2 infection in hematologic patients were developed in the very difficult context of dealing with novel viral variants from one pandemic wave to another, with different susceptibility to available drugs and vaccines. Moreover, the largest SARS-COV-2 case series in patients treated for hematologic malignancies, including stem cell transplant recipients, was published before the Omicron surge, and refers mainly to Alpha and Delta viral variants. These infections had very high mortality, in a period when antivirals and monoclonal antibodies were mostly unavailable. Here, we report for the first time a SARS-COV-2 Omicron variant outbreak inside a Bone Marrow Transplant (BMT) Unit, describing the characteristics, clinical course, and infection outcomes shortly before and shortly after myeloablative transplantation. We detail how infections were treated off-label and managed inside the BMT ward, to guarantee the best possible outcomes while avoiding risks for non-infected inpatients. The positive outcomes observed suggest that it may not be absolutely necessary to obtain SARS-CoV-2 PCR negativity before BMT in hematologic patients after treated infection, in cases with long-term PCR positivity and high-risk hematologic disease.


Assuntos
COVID-19 , Transplante de Células-Tronco Hematopoéticas , Humanos , SARS-CoV-2 , Surtos de Doenças , Transplante de Células-Tronco Hematopoéticas/efeitos adversos
2.
Infection ; 51(5): 1577-1581, 2023 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-37076752

RESUMO

PURPOSE: People with hematologic malignancies have a significantly higher risk of developing severe and protracted forms of SARS-CoV-2 infection compared to immunocompetent patients, regardless of vaccination status. RESULTS: We describe two cases of prolonged SARS-CoV-2 infection with multiple relapses of COVID-19 pneumonia in patients with follicular lymphoma treated with bendamustine and obinutuzumab or rituximab. The aim is to highlight the complexity of SARS-CoV-2 infection in this fragile group of patients and the necessity of evidence-based strategies to treat them properly. CONCLUSIONS: Patients with hematological malignancies treated with bendamustine and anti-CD20 antibodies had a significant risk of prolonged and relapsing course of COVID-19. Specific preventive and therapeutic strategies should be developed for this group of patients.


Assuntos
COVID-19 , Neoplasias Hematológicas , Linfoma Folicular , Humanos , Rituximab/uso terapêutico , Linfoma Folicular/complicações , Linfoma Folicular/tratamento farmacológico , Linfoma Folicular/patologia , Cloridrato de Bendamustina/uso terapêutico , Recidiva Local de Neoplasia/tratamento farmacológico , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , SARS-CoV-2 , Neoplasias Hematológicas/tratamento farmacológico
3.
J Med Virol ; 93(11): 6292-6300, 2021 11.
Artigo em Inglês | MEDLINE | ID: mdl-33580523

RESUMO

Human cytomegalovirus (CMV) represents the most common viral infection after hematopoietic stem cell transplant (HSCT), mainly occurring as reactivation from latency in seropositive patients, with a different prevalence based on the extent and timing of seroconversion in a specific population. Here, we retrospectively analyzed a cohort of patients who underwent HSCT at our Institution between 2013 and 2018, all of whom were prophylactically treated with CMV-IG (Megalotect Biotest®), to define the incidence and clinical outcomes of CMV reactivation and clinically significant infection. CMV infection occurred in 69% of our patient series, mainly resulting from reactivation, and CMV clinically significant infection (CS-CMVi) occurred in 48% of prophylactically treated patients. CMV infection and CS-CMVi impacted neither on relapse incidence nor on overall survival nor on relapse-free survival. Moreover, a very low incidence of CMV end-organ disease was documented. CMV-IG used alone as prophylactic therapy after HSCT does not effectively prevent CMV reactivation.


Assuntos
Anticorpos Antivirais/administração & dosagem , Infecções por Citomegalovirus/prevenção & controle , Citomegalovirus/fisiologia , Transplante de Células-Tronco Hematopoéticas/efeitos adversos , Imunoglobulina G/administração & dosagem , Ativação Viral , Adolescente , Adulto , Anticorpos Antivirais/imunologia , Antivirais/administração & dosagem , Antivirais/imunologia , Citomegalovirus/genética , Infecções por Citomegalovirus/imunologia , Infecções por Citomegalovirus/virologia , Feminino , Transplante de Células-Tronco Hematopoéticas/estatística & dados numéricos , Humanos , Masculino , Pessoa de Meia-Idade , Profilaxia Pré-Exposição , Recidiva , Estudos Retrospectivos , Adulto Jovem
4.
Int J Syst Evol Microbiol ; 65(Pt 2): 656-662, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-25487637

RESUMO

Fourteen mycobacterial strains isolated from pulmonary samples of independent patients in the state of Pará (Brazil), and three strains isolated in Italy, were characterized using a polyphasic approach. Thorough genetic investigation, including whole-genome sequencing, demonstrated that the strains belong to the M. simiae complex, being most closely related to Mycobacterium interjectum. For 14 of the strains, evidence emerged supporting their inclusion in a previously unreported species of the genus Mycobacterium, for which the name Mycobacterium paraense sp. nov. is proposed (type strain, IEC26(T) = DSM 46749(T) = CCUG 66121(T)). The novel species is characterized by slow growth, unpigmented or pale yellow scotochromogenic colonies, and a HPLC mycolic acid profile different from other known mycobacteria. In different genetic regions, high sequence microheterogeneity was detected.


Assuntos
Infecções por Mycobacterium/microbiologia , Mycobacterium/classificação , Filogenia , Técnicas de Tipagem Bacteriana , Brasil , DNA Bacteriano/genética , Genes Bacterianos , Humanos , Itália , Dados de Sequência Molecular , Mycobacterium/genética , Mycobacterium/isolamento & purificação , Ácidos Micólicos/química , RNA Ribossômico 16S/genética , Análise de Sequência de DNA , Escarro/microbiologia
5.
J Med Virol ; 85(1): 105-9, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23073996

RESUMO

Testicular germ cell tumors account for about 1% of all cancers. The incidence of these tumors is increasing and they represent the most common solid malignancies of young men aged 15-40 years with seminoma being one of the most common histotype. Pathogenesis of testicular germ cell tumors remains unknown and, although cryptorchidism is considered the main risk factor, there is evidence of an association with environmental and genetic risk factors. Human papillomaviruses (HPV) are a family of DNA viruses and represent a major risk factor for cervical cancer. In addition, they have been associated with other human non-malignant and malignant diseases, including breast and head and neck cancer. HPV sequences have been detected throughout the male lower genitourinary tract as well as in seminal fluid and an increased testicular tumorigenesis has been reported in HPV transgenic mice. Aim of this study was to evaluate the potential involvement of HPV in human testicular tumorigenesis. Real-time PCR employing GP5+/GP6+ consensus HPV primers was used to examine the presence of HPV sequences in a subset of human seminoma (n = 61) and normal testicles (n = 23). None of the specimens tested displayed the presence of HPV DNA. These findings do not support an association between HPV and human seminoma and warrant further studies to assess definitively the role of these viruses in human testicular tumorigenesis.


Assuntos
Papillomaviridae/isolamento & purificação , Infecções por Papillomavirus/complicações , Infecções por Papillomavirus/virologia , Seminoma/etiologia , Seminoma/virologia , Animais , Primers do DNA/genética , Humanos , Masculino , Camundongos , Camundongos Transgênicos , Papillomaviridae/genética , Reação em Cadeia da Polimerase/métodos , Proteínas Estruturais Virais/genética
6.
Nat Commun ; 2: 321, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21610724

RESUMO

Understanding the determinants of virus transmission is a fundamental step for effective design of screening and intervention strategies to control viral epidemics. Phylogenetic analysis can be a valid approach for the identification of transmission chains, and very-large data sets can be analysed through parallel computation. Here we propose and validate a new methodology for the partition of large-scale phylogenies and the inference of transmission clusters. This approach, on the basis of a depth-first search algorithm, conjugates the evaluation of node reliability, tree topology and patristic distance analysis. The method has been applied to identify transmission clusters of a phylogeny of 11,541 human immunodeficiency virus-1 subtype B pol gene sequences from a large Italian cohort. Molecular transmission chains were characterized by means of different clinical/demographic factors, such as the interaction between male homosexuals and male heterosexuals. Our method takes an advantage of a flexible notion of transmission cluster and can become a general framework to analyse other epidemics.


Assuntos
Classificação/métodos , Infecções por HIV/virologia , HIV-1/classificação , Filogenia , Algoritmos , Feminino , Produtos do Gene pol/genética , Infecções por HIV/transmissão , HIV-1/genética , HIV-1/isolamento & purificação , Humanos , Masculino
7.
Int J Syst Evol Microbiol ; 61(Pt 7): 1606-1611, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20693362

RESUMO

Four strains isolated in the last 15 years were revealed to be identical in their 16S rRNA gene sequences to MCRO19, the sequence of which was deposited in GenBank in 1995. In a polyphasic analysis including phenotypic and genotypic features, the five strains (including MCRO19), which had been isolated in four European countries, turned out to represent a unique taxonomic entity. They are scotochromogenic slow growers and are genetically related to the group that included Mycobacterium simiae and 15 other species. The novel species Mycobacterium europaeum sp. nov. is proposed to accommodate these five strains. Strain FI-95228(T) ( = DSM 45397(T)  = CCUG 58464(T)) was chosen as the type strain. In addition, a thorough revision of the phenotypic and genotypic characters of the species related to M. simiae was conducted which leads us to suggest the denomination of the 'Mycobacterium simiae complex' for this group.


Assuntos
Micobactérias não Tuberculosas/classificação , Filogenia , Adulto , Idoso de 80 Anos ou mais , Técnicas de Tipagem Bacteriana , Parede Celular/química , DNA Bacteriano/genética , Europa (Continente) , Feminino , Genótipo , Humanos , Masculino , Dados de Sequência Molecular , Infecções por Mycobacterium/microbiologia , Ácidos Micólicos/química , Micobactérias não Tuberculosas/genética , Micobactérias não Tuberculosas/isolamento & purificação , Fenótipo , RNA Ribossômico 16S/genética , Análise de Sequência de DNA
8.
Eur J Haematol ; 85(1): 76-82, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20148942

RESUMO

Clinical charts from 63 consecutive highly immunocompromised haematologic patients presenting with pulmonary nodular lesions on CT scan, classified as either probable or possible invasive fungal disease (IFD) according to the revised EORTC/MSG classification, were retrospectively studied. Histopathological analysis of lung tissues, available for 23 patients, demonstrated proven IFD in 17 cases (14 invasive aspergillosis and 3 invasive zygomycosis), diffuse alveolar damage in one and organising pneumonia (OP) in five cases. In the OP cases, three of which have been defined as probable IFD according to EORTC/MSG classification, extensive immunohistochemical, molecular and immunological analyses for fungi were negative. Our case descriptions extend the notion that OP may be encountered as a distinct histopathological entity in pulmonary nodular lesions in patients with leukaemia with probable/possible IFD.


Assuntos
Pneumonia em Organização Criptogênica/diagnóstico , Pneumonia em Organização Criptogênica/etiologia , Leucemia Mieloide Aguda/complicações , Pneumopatias Fúngicas/diagnóstico , Pneumopatias Fúngicas/etiologia , Idoso , Líquido da Lavagem Broncoalveolar/microbiologia , Diagnóstico Diferencial , Feminino , Humanos , Hospedeiro Imunocomprometido , Aspergilose Pulmonar Invasiva/diagnóstico , Aspergilose Pulmonar Invasiva/etiologia , Leucemia Mieloide Aguda/imunologia , Masculino , Pessoa de Meia-Idade , Infecções Oportunistas/diagnóstico , Infecções Oportunistas/etiologia , Estudos Retrospectivos , Zigomicose/diagnóstico , Zigomicose/etiologia
9.
Am J Hematol ; 85(3): 188-9, 2010 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19507207
11.
Diagn Microbiol Infect Dis ; 59(1): 81-4, 2007 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-17532594

RESUMO

We report an unusual case of documented Bartonella henselae genotype I from hepatic tissue in an Italian immunocompetent girl presenting with erythema nodosum and hepatic granulomata. Polymerase chain reaction (PCR) was performed on biopsied liver sample to confirm the etiologic role of B. henselae and to identify the genetic variant of this organism. A PCR on the same liver biopsy for parvovirus B19 was also positive, but the clinical meaning of this was not clear.


Assuntos
Infecções por Bartonella/diagnóstico , Bartonella henselae/genética , Eritema Nodoso/etiologia , Parvovirus B19 Humano/genética , Antibacterianos/uso terapêutico , Infecções por Bartonella/complicações , Infecções por Bartonella/tratamento farmacológico , Bartonella henselae/classificação , Pré-Escolar , Claritromicina/uso terapêutico , Eritema Nodoso/tratamento farmacológico , Feminino , Granuloma/tratamento farmacológico , Granuloma/microbiologia , Humanos , Imunocompetência , Hepatopatias/tratamento farmacológico , Hepatopatias/microbiologia , Infecções por Parvoviridae/complicações , Infecções por Parvoviridae/diagnóstico , Infecções por Parvoviridae/genética , Reação em Cadeia da Polimerase
12.
Transplantation ; 80(12): 1742-8, 2005 Dec 27.
Artigo em Inglês | MEDLINE | ID: mdl-16378070

RESUMO

BACKGROUND: Infectious complications still represent a major cause of morbidity and mortality in patients with organ transplantation. In particular, small bowel or multivisceral transplantation is complicated to a greater extent than other grafts as a consequence of infectious complications including sepsis. METHODS: This prospective study assessed outcome, incidence, and timing of infections in sequential patients undergoing small bowel or multivisceral transplantation (SB/MVTx) performed at a university transplant center between January 2001 and October 2003. Nineteen patients underwent transplantation during this period, 13 of whom (68%) undergoing isolated SB and 6 (32%) MV grafts with or without liver. RESULTS: The median follow up was 524 days (interquartile range=252-730) with an overall 24.4 person/year of observation. Postoperative mortality rate was 0.1 death/person/year; all patients, except one who died intraoperatively, were alive 6 months postsurgery. There were 100 documented infections including: 59 bacterial (2.4 events/person/year), 35 viral (1.4 events/person/year) and 6 fungal (0.2 events/person/year). Patients developed at least one episode of bacterial infection in 94% of the cases, viral infection in 67%, and fungal infection in 28%. CONCLUSIONS: This cohort describes the very common and complex nature of infectious complications in this challenging group of transplantation patients. Larger cohorts are needed to specifically address infection risk factors and longer term outcomes.


Assuntos
Intestino Delgado/transplante , Complicações Pós-Operatórias/epidemiologia , Infecção da Ferida Cirúrgica/epidemiologia , Transplante Homólogo/efeitos adversos , Vísceras/transplante , Adulto , Infecções Bacterianas/epidemiologia , Transfusão de Sangue , Causas de Morte , Feminino , Seguimentos , Rejeição de Enxerto/epidemiologia , Humanos , Incidência , Transplante de Fígado/efeitos adversos , Transplante de Fígado/mortalidade , Masculino , Micoses/epidemiologia , Reoperação , Estudos Retrospectivos , Análise de Sobrevida , Fatores de Tempo , Transplante Homólogo/mortalidade , Resultado do Tratamento , Viroses/epidemiologia
13.
Eur J Epidemiol ; 20(6): 559-61, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-16121766

RESUMO

The case of authoctonous isolated laryngeal leishmaniasis due to L. infantum in an italian immunocompetent host is reported. It is highlighed the need to consider mucosal leishmaniasis in the differential diagnosis of laryngeal tumors. Rapid nested-PCR technique and enzyme restriction analysis were useful for diagnosis and species identification directly from bioptic samples.


Assuntos
Hospedeiro Imunocomprometido , Neoplasias Laríngeas/diagnóstico , Leishmania infantum/isolamento & purificação , Leishmaniose/diagnóstico , Mucosa/parasitologia , Animais , Diagnóstico Diferencial , Humanos , Itália , Leishmaniose/imunologia , Leishmaniose/parasitologia , Masculino , Pessoa de Meia-Idade , Reação em Cadeia da Polimerase , Resultado do Tratamento
14.
Mod Pathol ; 18(2): 283-9, 2005 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-15272281

RESUMO

Ameloblastomas are epithelial tumors of odontogenic origin, biologically characterized by local recurrence. Among different etiologic factors, HPV infection has been recently postulated to be somehow involved in ameloblastoma etiopathogenesis. To address this issue, we studied 18 ameloblastomas by means of immunohistochemistry, in situ hybridization (conventional and amplified), polymerase chain reaction and nested-polymerase chain reaction analyses using laser capture microdissection in order to detect the occurrence of HPV in this setting. No evidence of HPV infection was detected by morphological examination, immunohistochemistry, in situ hybridization and conventional polymerase chain reaction, while nested-polymerase chain reaction showed a weak positive band in two cases. However, the subsequent restriction enzyme analysis carried out from the nested-polymerase chain reaction amplification products of these two samples excluded the presence of HPV subtypes 16, 18, 31, 33, 35, 52, and 58. The search for HPV 6 and 11 in the same specimens was also negative. In conclusion, our data do not support an etiopathogenetic evidence for HPV in ameloblastoma.


Assuntos
Ameloblastoma/patologia , Neoplasias Maxilomandibulares/patologia , Papillomaviridae/genética , Infecções por Papillomavirus/complicações , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Ameloblastoma/etiologia , Feminino , Humanos , Imuno-Histoquímica , Hibridização In Situ , Neoplasias Maxilomandibulares/etiologia , Masculino , Microdissecção/instrumentação , Microdissecção/métodos , Pessoa de Meia-Idade , Proteínas Oncogênicas Virais/análise , Proteínas Oncogênicas Virais/genética , Papillomaviridae/fisiologia , Infecções por Papillomavirus/virologia , Reação em Cadeia da Polimerase
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