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pubmed-article:8205562pubmed:abstractTextWe have investigated the effect of interferon beta (INF beta) on the natural killer (NK) cytotoxic activity of peripheral blood mononuclear cells (PBMC) from patients with superficial and infiltrative transitional-cell carcinoma of the bladder (TCC) against both NK-sensitive and NK-resistant target cells. The normal NK activity found in PBMC from these patients can be significantly enhanced by short-term incubation (18 h) with INF beta (P < 0.05). The depressed NK cytotoxic activity found in PBMC from patients with infiltrative TCC can also be significantly enhanced, but not normalized, by short-term incubation with INF beta (P < 0.05). In kinetic studies we found that the maximal levels of the INF beta-promoted cytotoxic activity against NK-sensitive and against NK-resistant target cells in PBMC from TCC patients were reached after 18 h of culture. Short-term-INF beta-incubated PBMC from patients with TCC of the bladder also showed marked cytotoxic activity against NK-resistant target cells. The effector cells of the INF beta-induced cytotoxic activity in PBMC from patients with TCC were CD16+ CD3- NK cells. This cytotoxic inducer effect of INF beta synergized with that of interleukin-2. In conclusion, INF beta can enhance the NK activity of PMBC from patients with TCC of the bladder.lld:pubmed
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pubmed-article:8205562pubmed:authorpubmed-author:OlivierCClld:pubmed
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pubmed-article:8205562pubmed:pagination406-10lld:pubmed
pubmed-article:8205562pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:8205562pubmed:articleTitleInterferon beta enhances the natural killer activity of patients with bladder carcinoma.lld:pubmed
pubmed-article:8205562pubmed:affiliationDepartment of Medicine, Hospital Universitario Principe de Asturias, Universidad de Alcalá de Henares, Madrid, Spain.lld:pubmed
pubmed-article:8205562pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8205562pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed