Association of recent HIV infection and in-utero HIV-1 transmission

被引:23
|
作者
Taha, E. Taha [2 ]
James, Maria M. [1 ]
Hoover, Donald R. [3 ,4 ]
Sun, Jin [2 ]
Laeyendecker, Oliver [5 ,6 ]
Mullis, Caroline E. [6 ]
Kumwenda, Johnstone J. [7 ]
Lingappa, Jairam R. [8 ,9 ,10 ]
Auvert, Bertran [11 ,12 ,13 ]
Morrison, Charles S. [14 ]
Mofensen, Lynne M. [15 ]
Taylor, Allan [16 ]
Fowler, Mary G. [1 ]
Kumenda, Newton I. [2 ]
Eshleman, Susan H. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD 21205 USA
[3] Rutgers State Univ, Dept Stat & Biostat, Piscataway, NJ USA
[4] Rutgers State Univ, Inst Hlth Healthcare Policy & Aging Res, Piscataway, NJ USA
[5] NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
[6] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[7] Univ Malawi, Dept Med, Coll Med, Blantyre, Malawi
[8] Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA
[9] Univ Washington, Dept Med, Seattle, WA USA
[10] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[11] INSERM, U1018, CESP, Villejuif, France
[12] Hop Ambroise Pare, AP HP, Boulogne, France
[13] Univ Versailles, Guyancourt, France
[14] Family Hlth Int, Clin Sci, Durham, NC USA
[15] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Pediat Adolescent & Maternal AIDS Branch, NIH, Rockville, MD USA
[16] Ctr Dis Control & Prevent, Epidemiol Branch, Div HIV AIDS Prevent, Atlanta, GA USA
基金
美国国家卫生研究院;
关键词
HIV; incidence; Malawi; mother-to-child transmission; multiassay algorithm; CAPTURE ENZYME-IMMUNOASSAY; TO-CHILD TRANSMISSION; PREGNANT-WOMEN; PREVENTION; RISK; RNA; PROPHYLAXIS; SELECTION; ASSAYS; STAGE;
D O I
10.1097/QAD.0b013e3283489d45
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: We previously developed a multiassay algorithm (MAA) to identify recent HIV infection that includes the BED-capture enzyme immunoassay, an avidity assay based on the Genetic Systems HIV-1/HIV-2+O enzyme immunoassay, CD4 cell count, and HIV viral load. We used this MAA to evaluate the association between recent maternal HIV infection and in-utero transmission of HIV. Methods: Plasma samples were collected at delivery from 2561 HIV-infected women in the postexposure prophylaxis of infants-Malawi trial. The MAA described above was used to identify women with recent HIV infection. Logistic regression models assessed association between recent HIV infection and in-utero HIV transmission (defined as a positive infant HIV DNA test at birth). Results: Seventy-three women were identified as recently infected using the MAA. Those women were younger and had lower parity than women who were identified as not recently infected using the MAA (P<0.0001 for age and parity). The frequency of in-utero HIV transmission was 17.8% among women identified as recently infected, compared with 6.7% among women identified as not recently infected (13/73 vs. 166/2488, P = 0.001). In a multivariate model, three factors were independently associated with in-utero HIV transmission: recent infection [adjusted odds ratio (AOR): 2.49, 95% confidence interval (CI): 1.30-4.78, P = 0.006], log(10) HIV viral load at delivery (AOR: 2.01, 95% CI: 1.60-2.51, P<0.0001), and younger age (per 10 year increase, AOR: 0.66, 95% CI: 0.43-0.93, P = 0.02). Conclusion: Results obtained using a MAA suggest that recent maternal HIV acquisition is strongly associated with in-utero HIV transmission, independent of HIV viral load at delivery. (C) 2011 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins
引用
收藏
页码:1357 / 1364
页数:8
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