Administration of live varicella vaccine to HIV-infected children with current or past significant depression of CD4+ T cells

被引:80
作者
Levin, MJ
Gershon, AA
Weinberg, A
Song, LY
Fentin, T
Nowak, B
机构
[1] Univ Colorado, Sch Med, Denver, CO 80262 USA
[2] Columbia Univ, New York, NY USA
[3] Frontier Sci & Technol Res Fdn Inc, Amherst, NY USA
[4] Harvard Univ, Sch Publ Hlth, Stat & Data Anal Ctr, Boston, MA 02115 USA
关键词
D O I
10.1086/505149
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Varicella can be a severe illness in human immunodeficiency virus (HIV)-infected children. The licensed, live attenuated varicella vaccine is safe and immunogenic in HIV-infected children with minimal symptoms and good preservation of CD4(+) T cells (Centers for Disease Control and Prevention immunologic category 1). Methods. To study the safety and immunogenicity of this vaccine in varicella-zoster virus (VZV)-naive, HIV-infected children with moderate symptoms and/or more pronounced past or current decreases in CD4+ T cell counts, such children (age, 1-8 years) received 2 doses of vaccine 3 months apart. The children were observed in a structured fashion for adverse events. Blood was tested for VZV antibody and VZV-specific cell-mediated immunity (CMI) at baseline, 8 weeks after each dose, and annually for 3 years. Subjects who had no evidence of immunity 1 year after vaccination received a third dose and were retested. Results. The vaccine was well tolerated; there were no vaccine-related, serious adverse events. Regardless of immunologic category, at least 79% of HIV-infected vaccine recipients developed VZV-specific antibody and/or CMI 2 months after 2 doses of vaccine, and 83% were responders 1 year after vaccination. Conclusions. HIV-infected children with a CD4+ T cell percentage of >= 15% and a CD4+ T cell count of >= 200 cells/mu L are likely to benefit from receiving varicella vaccine.
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页码:247 / 255
页数:9
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