Cytomegalovirus (CMV) and human immunodeficiency virus (HIV) burden, CMV end-organ disease, and survival in subjects with advanced HIV infection (AIDS clinical trials group protocol 360)

被引:53
|
作者
Erice, A
Tierney, C
Hirsch, M
Caliendo, AM
Weinberg, A
Kendall, MA
Polsky, B
机构
[1] Univ Minnesota, Minneapolis, MN USA
[2] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
[4] Emory Univ, Sch Med, Atlanta, GA USA
[5] Univ Colorado, Denver, CO 80202 USA
[6] Columbia Univ, Coll Phys & Surg, New York, NY USA
关键词
D O I
10.1086/375843
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We undertook a prospective study to analyze cytomegalovirus (CMV) end-organ disease ( EOD) in subjects with advanced human immunodeficiency virus (HIV) infection. Of 403 individuals without prior CMV EOD who were followed up for a median of 151 weeks, 56 died and 21 developed CMV EOD. Twenty of the subjects with CMV EOD had CD4 cell counts of less than or equal to50 cells/mm(3) and HIV RNA level of >10,000 copies/mL of plasma at baseline; in these 20 subjects, an increase of CMV DNA level to greater than the quantification limits was associated with CMV EOD. A CD4 cell count of less than or equal to100 cells/ mm(3) and an HIV RNA level of >10,000 copies/ mL of plasma at baseline, a CMV DNA level of >200 copies/ mL of blood during follow-up, or development of CMV EOD were all associated with decreased survival. HIV-infected subjects with CD4 cell counts of less than or equal to50 cells/mm(3) and HIV RNA levels of >10,000 copies/ mL of plasma should have blood fractions screened for CMV DNA; if CMV DNA is detected, CMV prophylaxis might be considered.
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收藏
页码:567 / 578
页数:12
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