HIV antiretroviral therapy and prevention use in US blood donors: a new blood safety concern

Author:

Custer Brian12ORCID,Quiner Claire13,Haaland Richard4ORCID,Martin Amy4,Stone Mars12ORCID,Reik Rita5,Steele Whitney R.6ORCID,Kessler Debra7,Williamson Phillip C.8,Anderson Steven A.9,Williams Alan E.9,Raymond Henry F.10,McFarland Willi11ORCID,Robinson William T.1213,Glick Sara14,Sey Kwa15,Melton C. David16,Glynn Simone A.17,Stramer Susan L.18,Busch Michael P.12ORCID

Affiliation:

1. Vitalant Research Institute, San Francisco, CA;

2. Department of Laboratory Medicine, University of California, San Francisco, San Francisco, CA;

3. RTI International, Research Triangle Park, NC;

4. Division of HIV/AIDS Prevention, US Centers for Disease Control and Prevention, Atlanta, GA;

5. OneBlood, St. Petersburg, FL;

6. Scientific Affairs, American Red Cross, Rockville, MD;

7. New York Blood Center, New York, NY;

8. Creative Testing Solutions, Tempe, AZ;

9. US Food and Drug Administration, Silver Spring, MD;

10. School of Public Health, Rutgers University, Piscataway, NJ;

11. San Francisco Department of Public Health, San Francisco, CA;

12. Louisiana Department of Health, New Orleans, LA;

13. Louisiana State University Health Sciences Center, New Orleans, LA;

14. Department of Medicine, University of Washington, Public Health–Seattle & King County, Seattle, WA;

15. Los Angeles Department of Health, Los Angeles, CA;

16. Georgia Department of Public Health, Atlanta, GA;

17. National Heart, Lung, and Blood Institute, National Institutes of Health, Rockville, MD; and

18. Scientific Affairs, American Red Cross, Gaithersburg, MD

Abstract

Abstract Antiretroviral therapy (ART) to treat and pre-exposure prophylaxis (PrEP) to prevent HIV infection are effective tools to help end the HIV epidemic. However, their use could affect HIV transfusion-transmission risk. Three different ART/PrEP prevalence analyses in blood donors were conducted. First, blood samples from HIV-positive and a comparison group of infection-nonreactive donors were tested under blind using liquid chromatography-tandem mass spectrometry for ART. Second, blood donor samples from infection-nonreactive, 18- to 45-year-old, male, first-time blood donors in 6 US locations were tested for emtricitabine and tenofovir. Third, in men who have sex with men (MSM) participating in the 2017 Centers for Disease Control and Prevention National HIV Behavioral Surveillance (NHBS) from 5 US cities, self-reported PrEP use proximate to donation was assessed. In blind testing, no ART was detected in 300 infection-nonreactive donor samples, but in 299 HIV confirmed-infected donor samples, 46 (15.4%; 95% confidence interval [CI], 11.5% to 20.0%) had evidence of ART. Of the 1494 samples tested from first-time male donors, 9 (0.6%; 95% CI, 0.03% to 1.1%) had tenofovir and emtricitabine. In the NHBS MSM survey, 27 of 591 respondents (4.8%; 95% CI, 3.2% to 6.9%) reported donating blood in 2016 or 2017 and PrEP use within the same time frame as blood donation. Persons who are HIV positive and taking ART and persons taking PrEP to prevent HIV infection are donating blood. Both situations could lead to increased risk of HIV transfusion transmission if blood screening assays are unable to detect HIV in donations from infected donors.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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