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Multicenter Study
. 2016 Mar;63(3):712-20.
doi: 10.1002/hep.28384. Epub 2016 Jan 16.

Acute and Chronic Hepatitis E Virus Infection in Human Immunodeficiency Virus-Infected U.S. Women

Affiliations
Multicenter Study

Acute and Chronic Hepatitis E Virus Infection in Human Immunodeficiency Virus-Infected U.S. Women

Mark H Kuniholm et al. Hepatology. 2016 Mar.

Abstract

Exposure to hepatitis E virus (HEV) is common in the United States, but there are few data on prevalence of HEV/human immunodeficiency virus (HIV) coinfection in U.S.

Populations: We tested 2,919 plasma samples collected from HIV-infected (HIV(+)) women and men enrolled in U.S. cohort studies for HEV viremia using a high-throughput nucleic acid testing (NAT) platform. NAT(+) samples were confirmed by real-time polymerase chain reaction. Samples were selected for testing primarily on the basis of biomarkers of liver disease and immune suppression. Prevalence of HEV viremia was 3 of 2,606 and 0 of 313 in tested plasma samples collected from HIV(+) women and men, respectively. All HEV isolates were genotype 3a. Based on follow-up testing of stored samples, 1 woman had chronic HEV infection for >4 years whereas 2 women had acute HEV detectable at only a single study visit.

Conclusions: To our knowledge, this is the first reported case of chronic HEV infection in an HIV(+) U.S. individual. We also confirm that chronic HEV infection can persist despite a CD4(+) count >200 cells/mm(3). Overall, though, these data suggest that HEV infection is rare in the HIV(+) U.S. population.

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Conflict of interest statement

CONFLICTS OF INTEREST

Edgar Ong and Jeffrey M. Linnen are employees of Hologic, Inc. which in partnership with Grifols Diagnostic Solutions (Emeryville, CA), developed the Procleix HEV assay. All other authors, no conflicts of interest declared.

Figures

Figure 1
Figure 1
HEV study design. *TMA assay; **in-house real-time PCR
Figure 2
Figure 2
Panels A–C. Patterns of ALT, AST, CD4+ count, HEV viremia and antibodies over time through 2013 for three women with confirmed HEV viremia (Panels A–C). ALT and AST are in IU/L and CD4+ counts are cells/mm3. The ± symbol represents an inconclusive or borderline test result. ALT and AST measurements in WIHS were conducted on an annual basis (every other WIHS visit) from 1994–2001 and on a semi-annual basis (every WIHS visit) thereafter. CD4+ measurements in WIHS are conducted on a semi-annual basis (every WIHS visit).
Figure 2
Figure 2
Panels A–C. Patterns of ALT, AST, CD4+ count, HEV viremia and antibodies over time through 2013 for three women with confirmed HEV viremia (Panels A–C). ALT and AST are in IU/L and CD4+ counts are cells/mm3. The ± symbol represents an inconclusive or borderline test result. ALT and AST measurements in WIHS were conducted on an annual basis (every other WIHS visit) from 1994–2001 and on a semi-annual basis (every WIHS visit) thereafter. CD4+ measurements in WIHS are conducted on a semi-annual basis (every WIHS visit).
Figure 2
Figure 2
Panels A–C. Patterns of ALT, AST, CD4+ count, HEV viremia and antibodies over time through 2013 for three women with confirmed HEV viremia (Panels A–C). ALT and AST are in IU/L and CD4+ counts are cells/mm3. The ± symbol represents an inconclusive or borderline test result. ALT and AST measurements in WIHS were conducted on an annual basis (every other WIHS visit) from 1994–2001 and on a semi-annual basis (every WIHS visit) thereafter. CD4+ measurements in WIHS are conducted on a semi-annual basis (every WIHS visit).

Comment in

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