Cytomegalovirus-specific immunity and protection against viremia and disease in HIV-infected patients in the era of highly active antiretroviral therapy

被引:26
作者
Weinberg, A
Tierney, C
Kendall, MA
Bosch, RJ
Bartlett, JP
Erice, A
Hirsch, MS
Polsky, B
机构
[1] Univ Colorado, Hlth Sci Ctr, Sch Med, Denver, CO 80262 USA
[2] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] Columbia Univ, Coll Phys & Surg, New York, NY 10027 USA
[5] St Lukes Roosevelt Hosp, New York, NY USA
[6] Hosp Asepey, Madrid, Spain
关键词
D O I
10.1086/499826
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To define the immune correlates of protection against cytomegalovirus ( CMV) end-organ disease, CMV-specific interferon ( IFN)-gamma enzyme-linked immunospot ( ELISPOT) and CD8(+) and CD4(+) intracellular IFN-gamma synthesis assays were performed for subjects with CD4(+) cell counts of <= 50 cells/mu L who were enrolled in a prospective observational study of CMV infection in the era of highly active antiretroviral therapy. Of 87 subjects, 46 developed viremia, 14 developed end-organ disease, and 20 died. Positive ELISPOT assay results, but not positive results for CD4(+) or CD8(+) intracellular IFN-gamma synthesis, were associated with delayed development of viremia and CMV end-organ disease or death. CMV viremia did not appear to boost CMV-specific immunity. ELISPOT assays may be used to identify HIV-infected patients who might benefit from anti-CMV prophylactic interventions.
引用
收藏
页码:488 / 493
页数:6
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