4.7 Article Proceedings Paper

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

期刊

JOURNAL OF INFECTIOUS DISEASES
卷 193, 期 4, 页码 488-493

出版社

UNIV CHICAGO PRESS
DOI: 10.1086/499826

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资金

  1. NCRR NIH HHS [RR-00036, RR-00051, RR-00046, RR-00070, RR-05096, RR-00034] Funding Source: Medline
  2. NIAID NIH HHS [AI-46370, AI-38855, AI-34832, AI-34853, AI-27666, AI-27673, AI-27664, AI-27663, AI-27661, AI-27660, AI-27658, AI-25924, AI-25903-15, AI-27675, AI-25897, AI-25879, AI-25868, AI-46386, AI-38858, AI-41089, AI-32783, AI-50410, AI-32782, AI-25859, AI--27659, AI-32770] Funding Source: Medline
  3. NICHD NIH HHS [HD-33345] Funding Source: Medline

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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.

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