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  3. A newly published AIDS study could open another front in the battle against HIV infection by showing that gene therapy can be us

A newly published AIDS study could open another front in the battle against HIV infection by showing that gene therapy can be us

admin2010-07-06  35
问题      A newly published AIDS study could open another front in the battle against HIV infection by showing that gene therapy can be used to stop infected cells from spreading the deadly virus, researchers said.
     In a test-tube experiment believed to be the first of its kind, researchers based at Children’s Hospital of Philadelphia were able to block the operation of the" tat "gene that allows HIV to spread throughout the body from infected cells.
     Up to now, genetic AIDS research has concentrated on finding ways to help healthy cells withstand the ravages of the HIV virus that infects an estimated 16, 000 new victims a day, mainly in the developing world.
     But by working with human cells already infected with HIV, the team was able to reduce the tat gene’s virus-replicating functions by 80 percent to 90 percent, according to findings published in the journal Gene Therapy.
     That, researchers said, raises the possibility of a new gene therapy approach capable of supplementing the current drug-based treatment known as highly active anti-retroviral therapy, or HAART, which is used to stop HIV infection from becoming full-blown AIDS.
     In recent studies, HAART has proved to be a costly drug regimen that poses serious side effects for HIV patients while delivering questionable results.
     "This is proof of the concept that HIV replication could be inhibited by a genetic approach, though we’re not at 100 percent yet, "said Dr. Stuart Starr, a study coauthor and chief of immunologic infectious diseases at Children’s Hospital.
     "Everyone thinks of an antiviral approach, or an immunologic approach to HIV. This adds another option into the equation that could become more important as other options prove not to be totally successful."
     Key to the study was an artificially produced" antitat" gene provided by the Washington-based Research Institute for Genetic and Human Therapy.
     Children’s Hospital researchers used a mouse retrovirus to deliver the antitat gene into HIV-infected U-1 and ACH-2 cells, which were developed in the lab from the tissues of living HIV patients.
     They found that when the antitat protein combined with the tat gene, it successfully inhibited the gene’s operation without disturbing healthy cells or causing toxic side-effects.
     The study, funded by a private foundation, also found that the introduction of the antitat gene prolonged the survival of immune-system cells called CD4 + T lymphocytes.
     Start said researchers have entered preliminary discussions with a New England-based primate center ,where animal experiments could be carried out on infected macaque monkeys.
     If animal experiments proved successful, the Children’s Hospital team would hope to have a gene therapy treatment ready for human clinical trials in three to four years.
According to Dr. Stuart Starr,______.
选项 A、the other options proved totally unsuccessful
B、everyone knows how to deal with HIV virus effectively
C、the new therapy is but one among a number of options
D、the new approach might take the place of other therapies
答案C
解析 A 其他的选择方案被证明是完全不成功的；B 每个人都知道如何有效地对抗艾滋病病毒；C 新的疗法是众多疗法中的一种；D 新的疗法可能会取代其他疗法。文章中提到了“This adds another．．．be totally successful．”说明了这增加了另一种选择方案，这种方案将变得越来越重要，因为其他治疗方案并不是完全成功的。故应选C 。
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