Hepatitis Delta: Seek and Ye Shall Find

The Journal of Infectious Diseases 2010;202:822–824
© 2010 by the Infectious Diseases Society of America. All rights reserved.
0022-1899/2010/20206-0002$15.00
DOI: 10.1086/655809

EDITORIAL COMMENTARY

Scott D. Holmberg and John W. Ward
Division of Viral Hepatitis, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia

Received 10 June 2010; accepted 10 June 2010; electronically published 11 August 2010.

(See the article by Kucirka et al, on pages 845–852.)

Reprints or correspondence: Dr Scott Holmberg, Division of Viral Hepatitis, Centers for Disease Control and Prevention, MS G‐37, 1600 Clifton Rd NE, Atlanta, GA 30333 (sdh1@cdc.gov).

Hepatitis delta virus (HDV) was discovered in 1977 by Rizzetto and colleagues [1], and—as he expressed it 30 years later—HDV “would have possibly died away as another odd antigenic subtype” of hepatitis B virus (HBV) had it not been for an international collaboration among investigators from Turin, Italy, the National Institutes of Health, and Georgetown University [2]. Chimpanzee experiments demonstrated that the delta antigen, rather than being a component of HBV, was its own defective form that required HBV for its infection and replication, a “virus’s virus.” Dual HBV‐HDV infection was quickly recognized to have worldwide distribution, to be associated with more severe and rapidly progressive hepatitis, and to be especially resistant to treatment.

In the past few decades, remarkable strides in understanding the complex interplay between HBV and HDV at the molecular level have been achieved [3]. But many mysteries remain when these insights are applied to human disease, in which levels of HBV DNA and HDV RNA may fluctuate in relation to each other or not at all in individual patients [4]. Furthermore, some of the groups with HBV‐HDV coinfection, such as injection drug users, also have hepatitis C virus (HCV) and human immunodeficiency virus (HIV) coinfections. Unrecognized coinfections with these viruses—ie, before the availability of reliable screening tests for HIV (1985) or HCV (1992)—may have confounded early observations of the clinical course of patients with HBV‐HDV coinfections. Indeed, one of the helpful observations of the article by Kucirka and colleagues [5] in the current issue of the Journal is the still very high infection rate found among a sample of injection drug users from 2005 to 2006 when tested for HCV (92%) or HIV (38%).

When first examined in the 1980s, it was clear that there were areas of high endemicity, especially in the Amazon Basin, Eastern Europe, and several regions of Africa and the Middle East, of intermediate endemicity in Southern Europe, and low endemicity in Northern Europe and North America. Over the next 10 years, there was a dramatic decline in HDV infection prevalence in Europe, considered to be the result of declining numbers of hepatitis B surface antigen (HBsAg)–positive injection drug users, vaccination for hepatitis B, and the effects of public health interventions related to the HIV epidemic. However, it has been noted that no additional declines in HDV have been observed in the past decade [6], perhaps because of the influx of immigrants dually infected with HBV‐HDV to the United States from highly endemic areas.

In the United States, several early studies in the late 1970s through the mid‐1980s showed antibodies to delta antigen in HBsAg‐positive blood donors (3.8%) in 1979 [7], persons with acute and chronic hepatitis B infection in Los Angeles (homosexual men, 15%; injection drug users, 22%) [8, 9], and developmentally disabled persons in Illinois state facilities (30%) [10]. Relatively high rates of HDV prevalence were seen in injection drug users in New York City (67%) [11]. Furthermore, a retrospective study of serum collected from 1972 to 1975 from drug‐using HBsAg‐positive patients at several Veterans Administration facilities at US locales showed that 42% had antibodies to delta antigen [12].

Few outbreaks of HDV in the United States (and these among injection drug users) have been detected and examined in the last 25 years. Over a 21‐month period between 1983 and 1985, Lettau and colleagues [13] investigated an outbreak of severe hepatitis among injection drug users in western Massachusetts associated with dual delta and hepatitis B viruses. Another 15 years elapsed before there was detection and investigation of a similar outbreak among injection drug users in Pierce County, Washington, by the Centers for Disease Control and Prevention (CDC) [14]. However, aside from these outbreaks, in recent years only about 6–10 cases of “confirmed” infections with HDV have been reported to the CDC from various states each year. Thus, it is quite difficult to know what is happening with HDV without specific reports such as the one by Kucirka and colleagues [5].

So, where is HDV headed in this country? On the one hand, there has been a gratifying decrease in prevalence of HDV in Asia and Europe, attributed to the expanding rate of hepatitis B vaccination activities over the last 20 years. We should expect a similar decline in HDV in the United States as we progressively remove its “host virus.” Or should we?

Previous outbreaks have shown a high prevalence of HDV coinfection among HBV‐infected injection drug users—54% in Massachusetts and 34.5% in Washington state—whereas HBV‐infected non‐drug users in those outbreaks had much lower HDV coinfection rates (9% in both states) [13, 14]. Indeed, a study of female prostitutes showed that, among those who used intravenous drugs, HBV and HDV coinfection rates were 21%, whereas the HBV‐infected women who were not injection drug users had an HDV coinfection rate of 6% [15]. Similarly, early analyses demonstrated high hepatitis D infection rates among hemophilic men (19%) [16] but not in gay men (0%) [17].

One unifying explanation for these numbers is that HDV, like other bloodborne pathogens, may be more efficiently transmitted parenterally than by sexual contact. If this is the case, perhaps we should not expect the same drop‐off in HDV coinfection rates as seen between 1980 and 2000 in places as diverse as Italy, Japan, Taiwan, and Turkey [6], where proportionately more HBV infection is acquired perinatally, sexually, or horizontally (in households), and proportionately less as the result of injection drug use. This hypothesis would also fit the current observation, albeit from a small sample, that fully 50% of HBV‐infected injection drug users in Baltimore in 2005–2006 had concurrent HDV infection.

Trends in HDV‐HBV coinfection and morbidity are contingent on successes in hepatitis B vaccination and screening. Approximately 15% of persons reported with acute hepatitis B infection in the United States are injection drug users [18]. In 1991, the United States adopted a vaccine‐based strategy to eliminate HBV transmission, with subsequent gains in immunization coverage particularly among children and adolescents [19]. Despite a long‐standing recommendation for hepatitis B vaccination, hepatitis B vaccine coverage among injection drug users remains low. As a result, 20%–70% of injection drug users have evidence of past or current HBV infection, with many lacking serologic evidence of hepatitis B vaccination and thus greater susceptibility to HBV [20]. When barriers to vaccination such as vaccine costs are removed, drug treatment centers successfully integrate hepatitis B vaccination as a routine service and greatly increase the numbers of injection drug users vaccinated [21]. To increase vaccination of injection drug users, the CDC recommends hepatitis B vaccination for all adults in correctional institutions and drug abuse prevention and treatment clinics; the CDC and other federal resources are available to defray the cost of vaccine purchase for these settings [19, 21]. In addition to vaccination, all injection drug users should be screened for HBV [19]. An estimated 3%–11% of injection drug users have chronic HBV infection, and many remain undiagnosed, reflecting inadequate HBV screening services in settings such as drug treatment programs [22]. Management of persons with chronic hepatitis B infection should include interventions to reduce behavioral risks of HBV transmission and referral for medical care. The data from Kucirka et al [5] highlight the importance of HDV testing as a component of clinical management for persons with chronic HBV infection. Unfortunately, few data are available to monitor whether injection drug users are receiving recommended hepatitis B prevention and care services.

Indeed, the study by Kucirka and colleagues [5] is not only useful as a marker of where we are in the US hepatitis D epidemic, but of where we are not. Very few studies such as this can or will be done, simply because there are too few cohorts of injection drug users currently being followed in the United States. The HIV/AIDS epidemic stimulated federal agencies such as the National Institute on Drug Abuse and (then) the CDC to establish studies of HIV and, eventually, of hepatitis virus infections among large populations of injection drug user in several cities. At present, the Baltimore study (ALIVE [AIDS Link to Intravenous Experience]) as reported here is the longest running US cohort study; in fact, its predecessor, “Man ALIVE,” predated the AIDS epidemic but is now one of few such studies left. This stymies our understanding not only of HDV and the “carrier” HBV epidemics in the United States but also of the continuing HCV and, to a lesser extent, HIV epidemics. Thus, we should expect our understanding of the evolution of the HDV epidemic—as well as HBV, HCV, and HIV epidemics—in this country, especially in one of the transmission risk groups most affected, to remain spotty and infrequent. It is a truism to write that “more research is needed,” but there is probably no more fitting comment on the implications of the research of the companion paper in this issue of the Journal.

References

•1.Rizzetto M, Canese MG, Gerin JL, et al. Immunofluorescence detection of new antigen‐antibody system (delta/anti‐delta) associated to hepatitis B virus in liver and serum of HBsAg carriers. Gut 1977;18(12):997–1003.

•2.Rizzetto M. Hepatitis D: thirty years after [review]. J Hepatol 2009;50:1043–1050.

•3.Taylor JM. Hepatitis delta virus. Virology 2006;344:71–76.

•4.Wedemeyer H. Re‐emerging interest in hepatitis delta: new insights into the dynamic interplay between HBV and HDV. J Hepatol 2010;52(5):627–629.

•5.Kucirka LM, Farzadegan H, Field JJ, et al. Prevalence, correlates, and viral dynamics of hepatitis delta among injection drug users. J Infect Dis 2010;202(6):845–852 (in this issue).

•6.Rizzetto M. Hepatitis D: the comeback? Liver Int 2009;29:140–142.

•7.Nath N, Mushawar IK, Fang CT, Berberian H, Dodd RY. Antibodies to delta antigen in asymptomatic hepatitis B surface antigen‐reactive blood donors in the United States and their association with other markers of hepatitis B virus. Am J Epidemiol 1985;122:218–225.

•8.De Cock KM, Niland JC, Lu HP, et al. Experience with human immunodeficiency virus infection in patients with hepatitis B virus and hepatitis delta virus infections in Los Angeles, 1977–1985. Am J Epidemiol 1988;127:1250–1260.

•9.Govindarajan S, Kanel GC, Peters RL. Prevalence of delta‐antibody among chronic hepatitis B virus infected patients in the Los Angeles area: its correlation with liver biopsy diagnosis. Gastroenterology 1983;85:160–162.

•10.Hershow RC, Chomel BB, Graham DR, et al. Hepatitis D virus infection in Illinois state facilities or the developmentally disabled: epidemiology and clinical manifestations. Ann Intern Med 1989;110:779–785.

•11.Novick DM, Farci P, Croxson TS, et al. Hepatitis D virus and human immunodeficiency virus antibodies in parenteral drug abusers who are hepatitis B surface antigen positive. J Infect Dis 1988;158:795–803.

•12.Ponzetto A, Seeff LB, Buskell‐Bales Z, et al. Hepatitis B markers in United States drug addicts with special emphasis on the delta hepatitis virus. Hepatology 1984;4:1111–1115.

•13.Lettau LA, McCarthy JG, Smith MH, et al. Outbreak of severe hepatitis due to delta and hepatitis B viruses in parenteral drug abusers and their contacts. N Engl J Med 1987;317:1256–1262.

•14.Bialek SR, Bower WA, Mottram K, et al. Risk factors for hepatitis B in an outbreak of hepatitis B and D among injection drug users. J Urban Health 2005;82:468–478.

•15.Rosenblum L, Darrow W, Witte J, et al. Sexual practices in the transmission of hepatitis B virus and prevalence of hepatitis delta virus infection in female prostitutes in the United States. JAMA 1992;267:2477–2481.

•16.Troisi CL, Hollinger FB, Hoots WK, et al. A multicenter study of viral hepatitis in a United States hemophilic population. Blood 1993;81:412–418.

•17.Weisfuse IB, Hadler SC, Fields HA, et al. Delta hepatitis in homosexual men in the United States. Hepatology 1989;9:872–874.

•18.Daniels D, Grytdal S, Wasley A. Surveillance for acute hepatitis—United States, 2007. MMWR 2009;58(Suppl 3):1–27.

•19.Centers for Disease Control and Prevention. A comprehensive immunization strategy to eliminate transmission of hepatitis B virus infection in the United States: recommendations of the Advisory Committee on Immunization Practices (ACIP). Part II: immunization of adults. MMWR Morb Mortal Wkly Rep 2006;55:1–33.

•20.Centers for Disease Control and Prevention. Recommendations for identification and public health management of persons with chronic hepatitis B virus infection. MMWR Morb Mortal Wkly Rep 2008;57:1–20.

•21.Kresina TF, Hoffman K, Lubran R, Clark HW. Integrating hepatitis services into substance abuse treatment programs: new initiatives from SAMHSA. Public Health Rep 2007;122(Suppl 2):96–98.

•22.Substance Abuse and Mental Health Services Administration, Center for Substance Abuse Treatment. Screening for infectious diseases among substance abusers (Treatment Improvement Protocol [TIP] Series 6; DHHS publication [SMA] 95–3060). Rockville, Maryland: NIH, 1993. http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=hssamhsatip&part=A25461. Accessed 19 April 2010.

Potential conflicts of interest: none reported.

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