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Clin Infect Dis. Oct 1, 2011; 53(7): 711–715.
PMCID: PMC3166351
John Cunningham Virus Antibody and Viremia as Predictors of Progressive Multifocal Leukoencephalopathy in Human Immunodeficiency Virus-1–Infected Individuals
Raphael P. Viscidi,corresponding author1a Nina Khanna,2,3 Chen S. Tan,4,5 Xiuhung Li,6 Lisa Jacobson,6 David B. Clifford,7 Avindra Nath,8 Joseph B. Margolick,9 Keerti V. Shah,9 Hans H. Hirsch,2,3a and Igor J. Koralnik4,5a
1Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland
2Division of Infectious Diseases and Hospital Epidemiology, and
3Institute for Medical Microbiology, Department of Biomedicine, University of Basel, Basel, Switzerland
4Department of Medicine, and
5Department of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts
6Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland
7Department of Neurology, Washington University School of Medicine, Saint Louis, Missouri
8Department of Neurology, Johns Hopkins University School of Medicine
9Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland
corresponding authorCorresponding author.
Correspondence: Raphael P Viscidi, MD, Johns Hopkins Hospital, Blalock Bldg Rm 1105, 600 N Wolfe St, Baltimore MD 21287 (rviscid1/at/jhmi.edu).
aR. P. V., H. H. H., and I. J. K. contributed equally to the study.
Received March 8, 2011; Accepted June 29, 2011.
Abstract
We examined whether prediagnostic John Cunningham virus (JCV) antibodies and viremia are predictors of progressive multifocal leukoencephalopathy (PML) in 83 PML cases and 240 human immunodeficiency virus (HIV) disease-matched controls. JCV viremia was not predictive of PML, but some patients showed higher anti-JCV immunoglobulin G (IgG) responses 6 months prior to diagnosis.
Progressive multifocal leukoencephalopathy (PML) is a demyelinating disease of the central nervous system caused by lytic infection of oligodendrocytes with John Cunningham polyomavirus (JCV). PML occurs in immunosuppressed individuals with AIDS or hematological malignancies, transplant recipients, and patients treated with immunomodulatory medications for autoimmune diseases [13].
Clinically useful predictors for PML are lacking. We therefore performed nested case-control studies within the Multicenter-AIDS and the Swiss-HIV (human immunodeficiency virus) cohort studies (MACS and SHCS) to examine whether JCV-specific virological and serological markers are predictors of PML.
The study was approved by the institutional review board (IRB) at each participating center and each MACS location.
Study Populations
Two nested case-control studies were performed using archived samples from the MACS, a prospective study of HIV/AIDS in homosexual men in the United States begun in 1984, and the SHCS, a prospective study of HIV-1 infected Swiss adults initiated in 1988. Demographic and clinical data, plasma, serum, and peripheral blood mononuclear cells (PBMC) were collected every 6 months for 2.5 years prior to PML diagnosis, and additionally for 1 year after diagnosis in the SHCS. Thirty PML patients from MACS were diagnosed between 1985 and 1996 by brain histology in 16 (53%), radiographic and clinical signs in 9 (30%), and clinical diagnosis in 5 (17%) patients. Cases were matched with 81 HIV-seropositive participants, who did not develop PML. In the SHCS, 53 patients were diagnosed with PML between 1995 and 2006 by brain histology in 7 (13%), detection of JCV by polymerase chain reaction (PCR) in cerebral spinal fluid in 18 (34%) and radiographic and clinical signs in 28 (53%) patients. Cases were matched with 149 HIV-seropositive participants. Criteria for matching are described in supplementary materials.
JCV PCR Assays
Plasma and PBMC samples were tested by quantitative PCR (QPCR) for JCV DNA (as described elsewhere [4] and supplementary materials).
JCV Serology Assays
A virus-like particle-based enzyme-linked immunosorbent assay (ELISA) was used to detect antibody to JCV capsids (as described elsewhere [5] and supplementary materials).
Statistical Analysis
Conditional logistic regression, with adjustment for age and CD4+ T-cell counts at diagnosis, was used to investigate the temporal relationship between PML and levels of log-transformed immunoglobulin (Ig) G, IgA, and IgM optical density values, serostatus, and plasma JCV DNA copy number.
Study Population
Within each study, demographic characteristics of cases and controls were similar (Table 1). MACS participants were men, while one-fifth of SHCS patients were women. Intravenous drug use was more common in SHCS (39.6%) than in MACS (12.6%). One case in MACS received combined antiretroviral therapy (cART), but 30 (57%) cases in SHCS were treated with cART. Within SHCS, cases and controls were well matched at entry and at PML diagnosis, while median CD4+ T-cell counts of MACS cases at the time of PML diagnosis were lower than that of controls (139 cells/uL vs 171 cells/uL, P = .01).
Table 1.
Table 1.
Characteristics of Study Populations
Serological Studies
Among the 83 PML cases and 230 controls, JCV IgG seroprevalence was 58% and 49%, respectively, 1–1.5 years before diagnosis, and did not differ substantially during other 6-month intervals before PML diagnosis. IgA seroprevalence among cases and controls 1–1.5 years before diagnosis was 16% and 11%, while IgM seroprevalence was 2.2% and 3.4%, respectively. After PML diagnosis, IgG seroprevalence increased to 96% in the 6 months following diagnosis, while IgA and IgM seroprevalence increased to 50% and 12.5%, respectively (analysis restricted to SHCS). Among subjects with 2 or more IgG measurements, 8 cases (15.1%) and 15 controls (9.4%) seroconverted. Fluctuating serostatus was observed in 8.6% of controls and 11.3% of cases. Treatment with cART had no effect on JCV-specific capsid IgG and IgM levels, whereas a trend for IgA seropositivity was seen (adjusted odds ratio [OR], 3.1, 95% confidence interval [CI], .99–9.74, P = .052).
The distribution of IgG, IgA, and IgM seroreactivity to JCV capsids during 6-month time intervals prior to PML diagnosis is shown in Figure 1. Six months prior to diagnosis, median (interquartile range) IgG levels for cases and controls were 0.23 (0.13, 0.40) and 0.18 (0.08, 0.35), respectively, and the median difference between matched case-control sets was 0.06 (−0.11, 0.23). Controlling for CD4+ T-cell count and age, a 1 log10 increase in JCV capsid-specific IgG level in cases compared with controls was associated with a 75% increase in the odds of developing PML (hazard ratio [HR], 1.75, 95% CI, 1.19–2.58, P = .0046). The association of IgG with risk of PML was observed in the combined analysis of 83 PML cases and in the 53 SHCS cases, but only a non-significant trend was seen in the 30 MACS cases. IgA and IgM levels were not associated with risk of PML. Comparable results were obtained when the analysis was restricted to the 36 PML cases confirmed histologically and/or virologically and their 114 controls. Antibodies to JCV capsid increased post PML diagnosis. The median IgG level was higher in SHCS cases compared with controls during the first 6-month interval (0.54 vs 0.24, P < .0001) and the 6–12 month interval (0.68 vs 0.23, P <.001) after diagnosis (Figure 2).
Figure 1.
Figure 1.
Distribution of IgG, IgA, and IgM absorbance values of sera from PML cases and HIV disease matched controls in the MACS and SHCS at time intervals before the diagnosis of PML. The summary statistics of each distribution are displayed in a box plot. The (more ...)
Figure 2.
Figure 2.
Distribution of absorbance values of IgG in sera from PML cases and HIV disease matched controls in the SHCS at time intervals before and after the diagnosis of PML. Data are represented in box plots as described in the legend to Figure 1.
Virological Studies
JCV DNA was detected by QPCR in plasma from 14 (17%) of 83 cases and 28 (12%) of 230 controls. The median detectable level of JCV DNA was 168 copy numbers per mL of plasma (interquartile range, 108–364). Detecting JCV viremia prior to diagnosis was not associated with a risk of developing PML. Of 42 subjects with viremia at 1 or more visits, 12 (29%) were seronegative at all visits. Six (26%) of 23 PML cases had detectable JCV DNA in PBMC samples during the 2 years prior to the diagnosis of PML, and the corresponding number for controls was 15 (17%) of 90 patients (P = .36).
We combined data from 2 nested case-control analyses to examine risk factors for development of PML in HIV-infected patients. Our study population of 83 PML cases is large for this rare disease. A striking finding was that JCV viremia did not have any diagnostic use for the risk of developing PML in the 2 years before diagnosis. The frequency of JC viremia in our study (13.4%) was lower than that reported for HIV-positive patients in some studies, which ranged between 20% and 40% [68].
The prevalence of IgG to JCV capsids and the level of antibody did not differ between cases and controls during any 6-month time window between 2.5 and 0.5 years before PML diagnosis. However, in the 6 months immediately preceding diagnosis of PML, the level of JCV capsid antibody was elevated in cases compared with controls, as reported elsewhere [9]. The association was largely due to the contribution of 53 cases from the SHCS. We cannot rule out that undefined technical and clinical factors, such as sample size, storage conditions, or the use of cART, contribute to this difference. The temporal proximity to the diagnosis of PML suggests that this association may reflect underlying disease. In a previous study in MACS, higher titers of JCV IgG were associated with JCV viruria but not to a diagnosis of PML [10] In total, 25% of HIV-positive individuals who developed PML were seronegative on 1 or more visits during the 2 years prior to diagnosis. It is not clear if seronegative patients were truly negative or if they had levels of antibodies too low to be scored as positive by our assay. In total, 29% of patients with JCV viremia were seronegative, supporting the notion that the assay was not very sensitive in the setting of advanced HIV infection. We speculate, therefore, that an increase in JCV IgG activity may reflect recent exposure to JCV antigen, which, in a severely immunosuppressed patient, might also indicate an increased risk of developing PML, while a stable IgG titer does not preclude subsequent development of PML.
One limitation of our study is the use of samples that had been kept frozen for long periods of time. It is possible that degradation of viral DNA precluded efficient amplification of JCV sequences. The JCV seroprevalence was lower in MACS (42%) than SHCS (67%) and lower than that reported in other populations [11, 12]. Nevertheless, the absence of viremia before PML diagnosis is consistent with models of pathogenesis, which hypothesize that PML is caused by reactivation in the brain either from virus resident in the brain or from virus in cells that traffic to the brain.
Interest in prediagnostic markers of PML has been triggered by the recent development of PML in multiple sclerosis and Crohn’s disease patients treated with natalizumab, and psoriasis patients treated with efalizumab [3]. The selective impairment in T-cell activation and trafficking caused by these drugs differs from immunosuppression seen in AIDS. Therefore, while it is not clear if the findings of our study are readily applicable to patients treated with these drugs, the study does suggest that monitoring these patients for JCV viremia is unlikely to predict who will develop PML.
Supplementary Data
Supplementary materials are available at Clinical Infectious Diseases online (http://www.oxfordjournals.org/our_journals/cid/). Supplementary materials consist of data provided by the author that are published to benefit the reader. The posted materials are not copyedited. The contents of all supplementary data are the sole responsibility of the authors. Questions or messages regarding errors should be addressed to the author.
Supplementary Data
Acknowledgments
Data in this manuscript were collected by the Multicenter AIDS Cohort Study (MACS) with centers (Principal Investigators) at the Johns Hopkins Bloomberg School of Public Health (Joseph B. Margolick, Lisa P. Jacobson), Howard Brown Health Center, Feinberg School of Medicine, Northwestern University, and Cook County Bureau of Health Services (John P. Phair, Steven M. Wolinsky), University of California, Los Angeles (Roger Detels), and University of Pittsburgh (Charles R. Rinaldo). Web site located at http://www.statepi.jhsph.edu/macs/macs.html.
The members of the Swiss HIV Cohort Study are M. Battegay, E. Bernasconi, J. Böni, HC. Bucher, Ph. Bürgisser, A. Calmy, S. Cattacin, M. Cavassini, R. Dubs, M. Egger, L. Elzi, M. Fischer, M. Flepp, A. Fontana, P. Francioli (President of the SHCS, Centre Hospitalier Universitaire Vaudois, CH-1011- Lausanne), H. Furrer (Chairman of the Clinical and Laboratory Committee), C. Fux, M. Gorgievski, H. Günthard (Chairman of the Scientific Board), H. H. Hirsch, B. Hirschel, I. Hösli, Ch. Kahlert, L. Kaiser, U. Karrer, C. Kind, Th. Klimkait, B. Ledergerber, G. Martinetti, B. Martinez, N. Müller, D. Nadal, M. Opravil, F. Paccaud, G. Pantaleo, A. Rauch, S. Regenass, M. Rickenbach (Head of Data Center), C. Rudin (Chairman of the Mother & Child Substudy), P. Schmid, D. Schultze, J. Schüpbach, R. Speck, P. Taffé, P. Tarr, A. Telenti, A. Trkola, P. Vernazza, R. Weber, S. Yerly.
We wish to thank Nadine Doppler from the institute for Medical Microbiology for technical assistance.
Financial support. This work was sponsored in part by grants from the Neurologic AIDS Research Consortium (U01 NS322228 to D. C. and I. J. K., R01 NS 041198, NS 047029, and K24 NS 060950); Johns Hopkins NIMH Center (5P30MH075673 to A. N.); and a Biogen Idec research grant (to I. J. K.). The MACS is funded by the National Institute of Allergy and Infectious Diseases, with additional supplemental funding from the National Cancer Institute (UO1-AI-35042, 5-MO1-RR-00052 [GCRC], UO1-AI-35043, UO1-AI-35039, UO1-AI-35040, UO1-AI-35041). This study has been supported by the Swiss HIV Cohort Study and the Swiss National Science Foundation (SHCS project Nr. 512).
Potential conflict of interest. D. C. has received fees for the following: consultancy from Biogen Idec, Genentech, Millennium, Genzyme, BMS, and Pfizer; expert testimony from Biogen Idec; payment for lectures or speakers bureaus from GSK, Millennium, Biogen; development of educational presentations from Millennium; travel/meeting expenses from Biogen Idec. A. N. has received fees for consultancy from Biogen and Diogenix. All other authors report no potential conflicts.
All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.
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