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1.
Clin Microbiol Infect ; 12(1): 50-5, 2006 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-16460546

RESUMO

Nasopharyngeal carriage of Streptococcus pneumoniae is a key factor in the development of invasive disease and the spread of resistant strains within the community. A single nasopharyngeal swab was obtained from 648 unvaccinated children aged <5 years, either healthy or with acute respiratory tract infection or meningitis, during the winters of 2000 and 2001. The overall pneumococcal carriage rate was 35.8% (95% CI 32.1-39.6). The pneumococcal serotypes found most frequently in the nasopharynx were 14, 6B, 6A, 19F, 10A, 23F and 18C, which included five of the seven serotypes in the currently licensed seven-valent conjugate vaccine (PCV7); serotypes 4 and 9V were less common. Serotypes 1 and 5 were isolated rarely from the nasopharynx. A comparison of 222 nasopharyngeal isolates with 125 invasive isolates, matched for age and time to the carrier isolates, showed a similar prevalence of penicillin non-susceptible pneumococci (PNSp) (19.8% and 19.2%, respectively). PNSp serotypes were similar (6B, 14, 19F, 19 A, 23B and 23F) for carriage and invasive disease isolates. The coverage of PCV7 for carriage isolates (52.2%) and invasive isolates (62.4%) did not differ significantly (p 0.06); similarly, there was no significant difference in PCV7 coverage for carriage isolates (34.5%) and invasive isolates (28.2%) of PNSp. These data suggest that PCV7 has the potential to reduce pneumococcal carriage and the number of carriers of PNSp belonging to vaccine serotypes.


Assuntos
Streptococcus pneumoniae/classificação , Antibacterianos/farmacologia , Brasil/epidemiologia , Portador Sadio/epidemiologia , Portador Sadio/microbiologia , Feminino , Humanos , Lactente , Masculino , Nasofaringe/microbiologia , Resistência às Penicilinas , Penicilinas/farmacologia , Infecções Pneumocócicas/epidemiologia , Infecções Pneumocócicas/microbiologia , Vacinas Pneumocócicas/administração & dosagem , Prevalência , Sorotipagem , Streptococcus pneumoniae/efeitos dos fármacos , Streptococcus pneumoniae/isolamento & purificação , Streptococcus pneumoniae/patogenicidade , Vacinação , Vacinas Conjugadas/administração & dosagem
2.
Lancet ; 358(9276): 91-7, 2001 Jul 14.
Artigo em Inglês | MEDLINE | ID: mdl-11463409

RESUMO

BACKGROUND: The yellow fever vaccine is regarded as one of the safest attenuated virus vaccines, with few side-effects or adverse events. We report the occurrence of two fatal cases of haemorrhagic fever associated with yellow fever 17DD substrain vaccine in Brazil. METHODS: We obtained epidemiological, serological, virological, pathological, immunocytochemical, and molecular biological data on the two cases to determine the cause of the illnesses. FINDINGS: The first case, in a 5-year-old white girl, was characterised by sudden onset of fever accompanied by headache, malaise, and vomiting 3 days after receiving yellow fever and measles-mumps-rubella vaccines. Afterwards she decompensated with icterus and haemorrhagic signs and died after a 5-day illness. The second patient-a 22-year-old black woman-developed a sore throat and fever accompanied by headache, myalgia, nausea, and vomiting 4 days after yellow fever vaccination. She then developed icterus, renal failure, and haemorrhagic diathesis, and died after 6 days of illness. Yellow fever virus was recovered in suckling mice and C6/36 cells from blood in both cases, as well as from fragments of liver, spleen, skin, and heart from the first case and from these and other viscera fragments in case 2. RNA of yellow fever virus was identical to that previously described for 17D genomic sequences. IgM ELISA tests for yellow fever virus were negative in case 1 and positive in case 2; similar tests for dengue, hantaviruses, arenaviruses, Leptospira, and hepatitis viruses A-D were negative. Tissue injuries from both patients were typical of wild-type yellow fever. INTERPRETATION: These serious and hitherto unknown complications of yellow fever vaccination are extremely rare, but the safety of yellow fever 17DD vaccine needs to be reviewed. Host factors, probably idiosyncratic reactions, might have had a substantial contributed to the unexpected outcome.


Assuntos
Injúria Renal Aguda/etiologia , Febre/etiologia , Cefaleia/etiologia , Hemorragia/etiologia , Icterícia/etiologia , Faringite/etiologia , Vômito/etiologia , Vacina contra Febre Amarela/efeitos adversos , Injúria Renal Aguda/epidemiologia , Injúria Renal Aguda/patologia , Adulto , Sistemas de Notificação de Reações Adversas a Medicamentos , Autopsia , Brasil/epidemiologia , Pré-Escolar , DNA Viral/análise , Ensaio de Imunoadsorção Enzimática , Evolução Fatal , Feminino , Febre/epidemiologia , Febre/patologia , Cefaleia/epidemiologia , Cefaleia/patologia , Hemorragia/epidemiologia , Hemorragia/patologia , Humanos , Imuno-Histoquímica , Icterícia/epidemiologia , Icterícia/patologia , Faringite/epidemiologia , Faringite/patologia , Alinhamento de Sequência , Vacinas Atenuadas/efeitos adversos , Vômito/epidemiologia , Vômito/patologia , Vírus da Febre Amarela/genética
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