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. Author manuscript; available in PMC: 2016 Oct 18.
Published in final edited form as: Exp Biol Med (Maywood). 2016 Mar 2;241(7):749–754. doi: 10.1177/1535370216636723

Parvovirus B19 Infection in Children with Sickle Cell Disease in the Hydroxyurea Era

Jane Hankins 1, Rhiannon R Penkert 2, Paul Lavoie 1, Li Tang 3, Yilun Sun 3, Julia L Hurwitz 2,4
PMCID: PMC4950380  NIHMSID: NIHMS817792  PMID: 26940953

Abstract

Parvovirus B19 infection causes transient aplastic crisis in sickle cell disease (SCD) due to a temporary interruption in the red blood cell production. Toxicity from hydroxyurea includes anemia and reticulocytopenia, both of which also occurring during a transient aplastic crisis event. Hydroxyurea inhibits proliferation of hematopoietic cells and may be immunosuppressive. We postulated that hydroxyurea could exacerbate parvovirus B19-induced aplastic crisis and inhibit the development of specific immune responses in children with SCD. We conducted a retrospective review of parvovirus B19 infection in 330 children with SCD. Altogether there were 120 known cases of aplastic crisis attributed to parvovirus B19 infection, and 12% of children were on hydroxyurea treatment during the episode. We evaluated hematological and immune responses. Children with HbSS or HbSβ0-thalassemia treated with hydroxyurea, when compared with untreated children, required fewer transfusions and had higher Hb concentration nadir during transient aplastic crisis. Duration of hospital stays was no different between hydroxyurea-treated and untreated groups. Children tested within a week following aplastic crisis disease were positive for parvovirus-specific IgG. Immune responses lasted for the duration of the observation period, up to 13 years after transient aplastic crisis, and there were no repeat aplastic crisis episodes. The frequencies of parvovirus-specific antibodies in all children with SCD increased with age, as expected due to the increased likelihood of a parvovirus exposure, and were comparable to frequencies reported for healthy children. Approximately one-third of children had a positive parvovirus B19-specific IgG test without a documented history of transient aplastic crisis, 64% of them were treated with hydroxyurea. Hydroxyurea may reduce requirements for blood transfusions and may attenuate symptoms during transient aplastic crisis episodes caused by parvovirus B19 infections. Children with SCD, whether treated or untreated with hydroxyurea, generate sustained and protective parvovirus B19-specific immune responses.

Keywords: sickle cell anemia, hydroxycarbamide, immune response

Introduction

Parvovirus B19 causes “fifth” disease, a common illness of childhood that is usually associated with low grade fever, malaise, arthralgia and a characteristic facial exanthem that resolves about two weeks after infection.1 In patients with sickle cell disease (SCD) however, parvovirus B19 infection exacerbates anemia by temporarily suppressing bone marrow erythropoietic activity, leading to a transient aplastic crisis episode that often requires hospitalization and supportive red blood cell transfusions.2-5 This complication is particularly common in young children with SCD, and less frequent, but present, in adults.6-8 In SCD patients, an acute parvovirus B19 infection event may also precipitate prolonged vaso-occlusive crisis, myocarditis, splenic sequestration, and fatal bone marrow embolism.9-12 Long-term parvovirus B19-associated problems in SCD can include glomerulonephritis (which may lead to end-stage renal disease), cardiac dysfunction, and stroke with permanent neurologic deficits.13;14 Acute and chronic complications arising from parvovirus B19 infection affect all SCD genotypes. In most individuals, including those with SCD, parvovirus B19 infection promotes the production of specific serum IgM and IgG antibodies and IgG-specific antibodies provide lifetime immunity from reinfection. In immunocompromised patients, however, acute parvovirus B19 infection can fail to resolve and produces severe and refractory anemia.15 These clinical observations raise the question as to whether hydroxyurea, an S-phase acting agent that inhibits hematopoietic cell proliferation, can impair clinical recovery during acute parvovirus B19 infection in SCD patients.

Hydroxyurea is a myelosupressive agent used with increasing frequency in the pediatric SCD population. Hydroxyurea therapy increases fetal hemoglobin production, hemoglobin (Hb) concentration and reduces white blood cell count and hemolysis markers, thereby ameliorating disease-associated symptoms and complications.16-18 Toxicities of hydroxyurea therapy in SCD include reversible, dose-related reticulocytopenia, neutropenia, and thrombocytopenia.19;20 Indeed, hydroxyurea therapy is most effective when dose-escalated to mild myelosuppression.21 Acute parvovirus B19 infection causes reticulocytopenia, and less commonly neutropenia, and thrombocytopenia, all of which are also reported as hydroxyurea toxicities. Moreover, hydroxyurea can potentially alter the immune response. A recent report demonstrated that total lymphocyte, CD4, and memory T-cell counts were reduced in hydroxyurea-treated children compared to placebo-treated controls, although these values were still within normal range.22

Little information exists in the literature regarding the hematopoietic effects and immune response during a natural parvovirus B19 infection in the context of hydroxyurea therapy. Defining the hematopoietic effects, immune response, and degree of protection elicited by natural infection in children with SCD treated with hydroxyurea is necessary: (i) to further evaluate the risk-benefit profile for hydroxyurea used in young children, (ii) to support vaccine development by defining a patient's potential to respond to parvovirus B19 antigens while receiving hydroxyurea therapy, and (iii) to provide benchmarks against which new vaccine candidates may be judged. To address these issues, we conducted a retrospective review of clinical parameters during a transient aplastic crisis episode and the parvovirus B19-specific immune responses in a large pediatric SCD population.

Methods

All participants were children with SCD treated at St. Jude Children's Research Hospital. The median age was 7.6 years (range 0.4 to 18 years). Inclusion criteria were: pediatric patients (age ≤18 years) with SCD (all genotypes) who were tested for parvovirus B19-specific antibody using the semi-quantitative commercially-available enzyme-linked immunosorbent assay (ELISA, Focus Diagnostics, Cypress, California, US) between June 2006 and December 2013. Parvovirus-specific immune responses, as reported by the manufacturer, were: negative <0.9, equivocal 0.9-1.1, and positive >1.1. Parvovirus B19 testing was performed due to suspicion of transient aplastic crisis, prior to initiation of hydroxyurea therapy, or as screening of prior viral exposure. In our program, we routinely screen young children for prior parvovirus B19 exposure (positive IgG) to help guide general management during a febrile event (e.g., help differentiate reticulocytopenia caused by transient aplastic crisis from a different virus) or hydroxyurea therapy (e.g., help differentiate reticulocytopenia caused by hydroxyurea toxicity from transient aplastic crisis).

The medical records of children with SCD who underwent a parvovirus ELISA test were reviewed for history of transient aplastic crisis and hydroxyurea therapy treatment. Transient aplastic crisis was defined as an exacerbation of anemia with severe reticulocytopenia (absolute reticulocyte count, ARC < 50 ×109/L),23 or a positive IgM score for parvovirus B19 (denoting acute infection). Parvovirus B19-specific serology was examined as a function of time relative to the transient aplastic crisis episodes. Duration of hospital stay, laboratory parameters, and erythrocyte transfusions (number of packed red blood cell, PRBC, units transfused) during the transient aplastic crisis event were compared between hydroxyurea-treated and hydroxyurea-untreated participants using Fisher's exact test or Wilcoxon-Mann-Whitney test, where appropriate. IRB approval was granted for this retrospective analysis, with a waiver of consent from participants.

Results

Transient aplastic crisis and hydroxyurea therapy

Of 330 eligible participants in our study, there were 120 who experienced an episode of transient aplastic crisis. The Hb genotype distribution of these 120 patients was HbSS (80), HbSC (30), HbSβ0-thalassemia (6), and HbSβ+-thalassemia (4). Fourteen (12%) patients who experienced aplastic crisis were treated with hydroxyurea for a median of 2.8 years (range 0.14 to 10.4 years) prior to this episode. In order to examine the severity of the transient aplastic crisis in relationship to hydroxyurea therapy, the initial and the nadir Hb concentration, ARC, duration of admission, and blood transfusion history were compared among the hydroxyurea treated and untreated groups, including all sickle genotypes. The proportion of participants given erythrocyte transfusion (for a significant decline from baseline or clinical symptoms of anemia) during the episode of transient aplastic crisis was similar among patients receiving hydroxyurea therapy compared to those who were not on hydroxyurea (Table 1). Children who were not treated with hydroxyurea (median age = 7.1, range 0.5 to 17.6 years), however, were more likely to receive > 1 unit of packed red blood cells than those treated with hydroxyurea (median age = 8.9, range 4.0 to 17.3 years) during the transient aplastic crisis (Table 1). There was no difference in Hb concentration and ARC at the onset or during nadir of the transient aplastic crisis episode (Table 1). The median duration of hospital stay between children receiving hydroxyurea and those who were not on this treatment was similar (2 versus 3 days, respectively, p=0.1). This analysis was repeated among hydroxyurea-treated and untreated children with HbSS or HbSβ0 thalassemia Hb genotypes only. The findings were similar, except that the group of hydroxyurea-treated patients exhibited a higher median Hb concentration nadir during aplastic crisis and were less likely to receive an erythrocyte transfusion in comparison with untreated patients (Table 1). The number of SCD-related complications (acute vaso-occlusive pain, acute chest syndrome and acute splenic sequestration) in the 4 weeks following the episode of transient aplastic crisis was similar among hydroxyurea-treated and untreated children. One child developed myocarditis during the episode of transient aplastic crisis, and she was not receiving hydroxyurea during this episode.

Table 1. Comparison of hematologic indices and erythrocyte transfusions according to therapy during the transient aplastic crisis episode.

Hydroxyurea-treated Hydroxyurea-Untreated P-value
All genotypes
(N=14) (N=106)
Baseline Hb (g/dL) 8.9 (7.3, 11.5) 9.2 (6.1, 11.9) 0.7a
Nadir Hb (g/dL) 6.5 (4.4, 8.6) 5.8 (2.1, 9.9) 0.1a
Nadir ARC (×109/L) 22.0 (1.3, 168.8) 14.0 (0, 319.0) 0.3a
# patients transfused (%) 10/14 (71%) 87/100 (87%) 0.2b
# patients who received >1 PRBC (%) 1/10 (10%) 37/76 (49%) 0.04b
HbSS and HbSβ0thalassemia
(N=14) (N=72)
Baseline Hb (g/dL) 8.9 (7.3, 11.5) 8.5 (6.1, 11.0) 0.1a
Nadir Hb (g/dL) 6.5 (4.4, 8.6) 5.2 (2.1, 8.7) 0.01a
Nadir ARC (×109/L) 22.0 (1.3, 168.8) 18.0 (0, 190.8) 0.7a
# patients transfused (%) 10/14 (71%) 62/66 (94%) 0.03b
# patients who received >1 PRBC (%) 1/10 (10%) 31/51 (61%) 0.005b
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Notes: Results presented as median (range) unless noted otherwise. Hb: hemoglobin concentration, ARC: absolute reticulocyte count, PRBC: packed red blood cell.

a

Wilcoxon-Mann-Whitney test was applied.

b

Fisher's Exact Test was applied.

B19 Parvovirus-specific immune response following a known aplastic crisis event

We next analyzed the timing of parvovirus B19-specific responses after documented transient aplastic crises. Parvovirus B19-specific IgM antibodies were not detected in IgG positive patients who exhibited no evidence of a current transient aplastic crisis, indicating a past infection. When tested prior to or greater than 7 days from the aplastic crisis episodes, the IgM antibodies were not present, however, when tested at the time of diagnosis of aplastic crisis, patients exhibited parvovirus B19-specific IgM antibodies (index>1.1), indicating a rapid primary response (Figure 1A). The IgG antibody response was evident at time periods shortly thereafter (Figure 1B). IgM responses quickly waned, whereas IgG responses were sustained for the duration of the observation period (up to 4976 days) in all patients who experienced transient aplastic crisis. Two individuals exhibited signs of transient aplastic crisis without a detectable IgG response, however since the antibody measurement was conducted only 4 days after the onset of symptoms (fever and reticulocytopenia), it likely preceded the IgG rise. These two participants were not receiving hydroxyurea at the time of the transient aplastic crisis episode. There were no cases of recurrent aplastic crisis among any patients in this cohort.

Figure 1. Parvovirus antibody scores in relationship with transient aplastic crisis events.

Figure 1

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Each dot represents a different blood sample tested for IgM (panel A) or IgG (panel B). IgM responses were observed immediately following the onset of symptoms and IgG responses were slightly delayed. IgG responses were long-lasting in all tested subjects.

There were no differences in the magnitude or timing of parvovirus-specific sero-responses among participants who were treated with hydroxyurea or not (p = 0.38 for IgG; p = 0.47 for IgM). After the transient aplastic crisis, an additional 35 participants initiated hydroxyurea therapy, yielding a total of 49 hydroxyurea-treated children. At a median of 0.6 years (range 0 to 9.1) after the transient aplastic crisis, these hydroxyurea-treated children continued to exhibit positive IgG scores that did not significantly differ in magnitude from those of untreated patients.

Parvovirus B-19 specific immune responses among all 330 children with SCD

We further analyzed the frequencies of anti-parvovirus B19 antibody production in all 330 pediatric SCD patients, regardless of hydroxyurea treatment or prior aplastic crisis, over a 7.5 year interval. Overall, 124 of 330 (38%) patients exhibited a positive IgG result. There were 387 valid observations in total, because some patients were tested more than once (Figure 2A). Positive scores in the first year of life (0.6% of events) could have occurred via maternal antibody transmission. A steady rise in anti-parvovirus B19 seropositivity among children with SCD was observed with increasing age (range 12 to 53%) (Figure 2B), as would be expected due to an increased likelihood of parvovirus B19 exposure over time.

Figure 2. IgG Seropositivity rates among children with SCD.

Figure 2

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A. Each point represents an individual sample. B. The fraction of children of various age groups with positive parvovirus-specific antibody responses increases with age.

Patients with parvovirus-specific IgG, but no record of parvovirus-induced aplastic crisis

Forty-four (35%) out of 124 participants with positive IgG did not have a documented history of prior transient aplastic crisis in their medical records. Of these, there were 23 patients for whom records were complete. Medical records were incomplete for the remaining 21 patients due to transfer from other programs or gaps in their care. Among the 23 with patients with complete records at the time of documentation of a positive IgG, 16 had HbSS or HbSβ0 thalassemia (15 of whom received hydroxyurea or monthly transfusion therapy), and 7 had HbSC or HbSβ+ thalassemia (3 of whom received hydroxyurea therapy). Of the remaining 21 patients for whom records were incomplete, 19 had HbSS or HbSβ0 thalassemia (17 of whom received hydroxyurea or monthly transfusion therapy), and 2 had HbSC or HbSβ+ thalassemia (none of them receiving any disease-modifying therapy). Overall, a greater proportion of children with IgG sero-positive tests without prior documented aplastic crises were treated with hydroxyurea than children with IgG sero-positive tests and prior documented aplastic crises (64% versus 12%).

Discussion

We studied 330 children with SCD including 120 who had suffered transient aplastic crisis, 12% of whom were treated with hydroxyurea. Hydroxyurea treatment was associated with a reduced requirement for transfused PRBCs and higher Hb concentration nadir during aplastic crisis events, although there was no difference in the duration of hospitalization. There was no difference in production of parvovirus B19-specific immunoglobulins with hydroxyurea therapy.

Because transient aplastic crisis and hydroxyurea toxicity both cause bone marrow suppression with ensuing reticulocytopenia and anemia, it is theoretically possible that children receiving hydroxyurea could experience worsened symptoms during transient aplastic crisis. Our findings refute this possibility as hematologic indices and duration of stay were not worse when accounting for hydroxyurea treatment. Indeed, our study suggests that concomitant hydroxyurea therapy may reduce the total volume of transfused red blood cells during aplastic crisis, which may be mediated by an increase in the lifespan of red blood cells in individuals with SCD, as reflected by a higher Hb concentration nadir among children with HbSS or HbSβ0 thalassemia. Red blood survival (as measured by 51Cr method) is indeed prolonged during therapy with hydroxyurea.24

In immunocompetent individuals, a first infection by parvovirus B19 usually provides lifelong protection against re-infection, although exceptions have been reported in SCD patients.25 In our cohort, no cases of re-infection were observed. The onset of aplastic crisis indicated the approximate time of parvovirus exposure for many patients and therefore provided a unique opportunity to monitor the kinetics of the humoral immune response. In our sample, IgM production was evident within a median of 1 day after clinical presentation and typically waned by 1 week. IgG responses were evident as early as the first day of symptom onset and were sustained for more than 13 years after infection. Among all patients with SCD, regardless of known exposure to parvovirus or hydroxyurea therapy, the frequency of parvovirus B19-specific antibody responses increased with age, as expected due to an increased likelihood of parvovirus B19 exposure over time. Frequencies of parvovirus-specific antibodies were similar to those of healthy children and other previously examined SCD pediatric populations.6;7;26;27

Positive IgG results were recognized in approximately one third of patients who had no documentation of prior transient aplastic crisis. This indicates that infection with parvovirus B19 does not cause clinically evident transient aplastic crisis in all SCD patients. Prior reports have shown prevalence of absent prior documented transient aplastic crisis in patients with parvovirus B19 IgG ranging from 20 to 35%, which is in agreement with our findings.6;28 In our study, several patients with parvovirus-specific antibodies without a documented history of worsened anemia and reticulocytopenia were receiving chronic transfusion therapy or harbored HbSC or HbSβ+ thalassemia genotypes. These situations increase the red blood cell lifespan and are therefore predicted to reduce the severity of transient aplastic crisis. Furthermore, passive parvovirus B19 IgG may occur during transfusions, possibly explaining the absence of documented history of transient aplastic crisis. Finally, 64% of these patients were treated with hydroxyurea, possibly minimizing symptoms of worsened anemia during transient aplastic crisis. Because we may have underreported the occurrence of prior transient aplastic crisis in some patients (due to incomplete records in 21 subjects), it is possible that the true rate of asymptomatic parvovirus B19 infection was lower than 35% in our population.

Our findings indicate that concomitant hydroxyurea therapy does not worsen parvovirus B19-induced transient aplastic crisis nor does it compromise immune responses that protect against repeat infections. However, there are several limitations to data interpretation. First, our study was retrospective with a relatively small number of participants on hydroxyurea at the time of the transient aplastic crisis. In addition, full records were not available on patients who had positive anti-parvovirus B19 IgG without prior documentation of transient aplastic crisis, and we were not able to retrieve total volume of transfused PRBCs on all participants (only total number of units). Finally, we could not exclude the possibility that clinicians' preferences for post-transfusion target Hb played a role in our results. However, we have formally investigated the relationships between hydroxyurea therapy and severity of transient aplastic crisis and the parvovirus B19-specific immune response, both of which will aid in the development of future vaccines and help to better define the relative risks and benefits of the drug. This information is particularly important considering that recent guidelines encourage caregivers to offer hydroxyurea therapy to all HbSS and HbSβ0-thalassemia children over age 9 months, regardless of severity of symptoms.29 Thus, use of this drug for SCD is likely to increase substantially in the near future.

In conclusion, we demonstrate that the responses to natural parvovirus B19 infection in children with SCD are predictable, protective, long-lasting and not worsened by concomitant hydroxyurea therapy. These data support other studies indicating that hydroxyurea therapy does not cause clinically significant immunosuppression22;30 and alleviate concerns that use of the drug could cause chronic or relapsed parvovirus B19 infection in SCD patients. Patients with SCD who are treated with hydroxyurea exhibit normal response to a natural parvovirus B19 infection and are likely to exhibit normal responses to candidate parvovirus B19 vaccines, therefore should not be excluded from related clinical trials.

Acknowledgments

This work was supported in part by the Children's Infectious Defense Center (CIDC), NIH R01 AI088729, NIH P30 CA21765, and the American Lebanese Syrian Associated Charities (ALSAC). The authors would like to thank Mitch Weiss, MD, PhD for critical editing of the manuscript, and Bertha Davis and Jola Dowdy, BS, MS for support with data collection and regulatory procedures.

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