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1.
Prostate Cancer Prostatic Dis ; 6(4): 301-4, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-14663471

RESUMO

This trial investigated the tolerability and effect of modified citrus pectin (Pecta-Sol) in 13 men with prostate cancer and biochemical prostate-specific antigen (PSA) failure after localized treatment, that is, radical prostatectomy, radiation, or cryosurgery. A total of 13 men were evaluated for tolerability and 10 for efficacy. Changes in the prostate-specific antigen doubling time (PSADT) of the 10 men were the primary end point in the study. We found that the PSADT increased (P-value<0.05) in seven (70%) of 10 men after taking MCP for 12 months compared to before taking MCP. This study suggests that MCP may lengthen the PSADT in men with recurrent prostate cancer.


Assuntos
Citrus , Pectinas/química , Pectinas/uso terapêutico , Antígeno Prostático Específico/sangue , Neoplasias da Próstata/sangue , Idoso , Humanos , Masculino , Pessoa de Meia-Idade , Pectinas/efeitos adversos , Testosterona/sangue
2.
Proc Natl Acad Sci U S A ; 100(8): 4819-24, 2003 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-12684537

RESUMO

Viral replication and latently infected cellular reservoirs persist in HIV-infected patients achieving undetectable plasma virus levels with potent antiretroviral therapy. We exploited a predictable drug resistance mutation in the HIV reverse transcriptase to label and track cells infected during defined intervals of treatment and to identify cells replenished by ongoing replication. Decay rates of subsets of latently HIV-infected cells paradoxically decreased with time since establishment, reflecting heterogeneous lymphocyte activation and clearance. Residual low-level replication can replenish cellular reservoirs; however, it does not account for prolonged clearance rates in patients without detectable viremia. In patients receiving potent antiretroviral therapy, the latent pool has a heterogeneous and dynamic composition that comprises a progressively increasing proportion of stable lymphocytes. Eradication will not be achieved with complete inhibition of viral replication alone.


Assuntos
Infecções por HIV/sangue , Infecções por HIV/virologia , Linfócitos/patologia , Linfócitos/virologia , Terapia Antirretroviral de Alta Atividade , Sobrevivência Celular , DNA Viral/sangue , DNA Viral/genética , Infecções por HIV/tratamento farmacológico , Transcriptase Reversa do HIV/genética , HIV-1/genética , HIV-1/isolamento & purificação , HIV-1/fisiologia , Humanos , Mutação Puntual , Fatores de Tempo , Viremia/sangue , Viremia/virologia , Replicação Viral
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