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Over a 5½-year period, 22 of 262 children receiving liver transplants developed adenoviral infections. Five had adenoviral hepatitis in the allograft, caused by serotype 5. All five were treated for rejection, either just before or at the time of infection. Liver biopsy specimens had characteristic histological appearance, and diagnosis of adenoviral infection was confirmed with monoclonal anti-adenoviral antibodies, electron microscopy, and by culture of liver tissue. In the remaining 17 patients, adenovirus was isolated from urine, stool, throat secretions, and/or blood samples, but none had any detectable visceral infection. Serotypes 1 and 2 predominated, similar to children not receiving transplants during the same time period. Three of the patients with hepatitis are alive and well; two died of liver failure. Adenoviral hepatitis did not recur in the second allograft of a patient who underwent retransplantation for combined rejection and adenoviral hepatitis, and appears, therefore, not to be a contraindication to retransplantation when liver failure ensues.
Since they were first isolated from human tissues in 1953,1 adenoviruses (AVs) have been shown to cause a wide spectrum of illness. Common forms of infection are pharyngitis, conjunctivitis, gastroenteritis, and pneumonia. It is believed that AVs cause 10% of pneumonias that require hospitalization in children2 and that by age 5 years every child has had at least one episode of AV infection.3 To date, 41 serotypes have been identified,4 and serotypes 1 to 3, 5 to 7, and 21 are the most common pathogens in children.2 Adenoviruses have been reported on occasion to cause fulminant hepatitis and other disseminated infections, mostly in immunocompromised patients,5–7 including renal and bone marrow transplant recipients.8–12 There is a case report of a lethal AV infection following a fetal liver transplant for severe combined immunodeficiency.13 A recent fatal AV hepatitis following orthotopic liver transplant in a child in our institution prompted us to review our experience with these infections in pediatric recipients of orthotopic liver transplants.
The records of the virology laboratory at Children’s Hospital of Pittsburgh were reviewed and all patients, including those receiving liver transplants from whom AV was isolated between March 1981 and September 1986 were identified. Clinical data of all patients with orthotopic liver transplants having AV infections were reviewed, with particular attention paid to the interval between transplantation and onset of infection, the relationship of rejection and its treatment to infection, other concomitant viral infections, and the clinical features of AV infections. All available, pertinent pathology material was reviewed by one of us (R.J.). Information regarding the site and serotype of AV was obtained for the nontransplant population.
Throat swab, urine, and blood specimens were sent for virologic culture every two weeks in all children with liver transplants as part of viral surveillance and during the investigation of any febrile episode (temperature of 38.5°C or more). Stool samples were sent only when patients developed diarrhea. Beginning in June 1985, liver tissue from biopsy specimens was sent routinely for viral culture. Urine and throat swab specimens were sent in viral transport medium containing a balanced salt solution, gelatin, and antibiotics. Blood was sent in a heparinized specimen tube; the buffy coat was separated and resuspended in viral transport medium. Liver tissue, submitted in a petri dish with saline, was ground with a mortar and centrifuged and the supernatant was added to viral transport medium. Specimens in viral transport medium were inoculated into commercially prepared cell culture tubes. One tube each of African green monkey kidney and HEp-2 cells and two tubes of human foreskin fibroblasts were used. Liver tissue was also inoculated into Rhesus monkey kidney and WI-38 cells. Cell culture tubes were maintained at 37°C and observed periodically for cytopathic effects. Cytomegalovirus (CMV) and herpes simplex were identified by their cytopathic effect alone. Suspected AV isolates were identified and typed at the Allegheny County (Pittsburgh) Laboratories using neutralization with antisera obtained from the Centers for Disease Control, on African green monkey kidney and HEp-2 cells.
Liver tissue was processed for light microscopy and a portion was snap frozen in a cryoprotective medium and stored at −70°C. Frozen sections were stained using an avidin-biotin peroxidase method with monoclonal anti-AV antibody (MA805) and anti-CMV antibody (MA810). The anti-AV antibody crossreacts with all serotypes and the anti-CMV antibody recognized an early antigen. Appropriate biologic positive and negative controls were used. Sections for electron microscopy were fixed in 2% glutaraldehyde, embedded in epoxy resin and examined with a Phillips II microscope.
During the 5½-year study period 262 children received orthotopic liver transplants. Immunosuppression was with cyclosporin and steroids. Rejection episodes were treated with additional steroids, monoclonal antibody OKT3, or both. Twenty-two patients (8.4%) had AV isolated from different sites. These patients were divided into two groups based on the type of infection.
All five patients in this group (Table 1) had hepatitis caused by AV serotype 5 (AV5) within an interval of 12 to 30 days following the transplant. All five had received treatment for suspected rejection either concurrently with the AV infection or shortly preceding it. Three of the five had the rejection episode treated with OKT3 in addition to other therapy. Four of the five patients showed growth of AV5 in other sites in addition to liver (blood, urine, and throat), but none had any other parenchymal organ involvement. Two of the five also had CMV infection while in three AV was the only viral infection. All had elevated serum transaminase levels and severe systemic symptoms (eg, temperatures to 40°C and chills) but only in one could the fevers be attributed entirely to AV as the others had, in addition, rejection or other infections. The diagnosis in all five was suspected by histological findings (four biopsy specimens and one hepatectomy specimen at retransplantation), and was confirmed by ancillary means. The patient undergoing retransplantation had both AV infection and rejection in the removed allograft. Three of the five patients are alive and well; two patients died of fulminant liver failure with coagulopathy and of gastrointestinal tract bleeding. Autopsies were performed on both.
The features in all five cases were highly distinctive and virtually identical. Punched-out, circumscribed lesions were scattered randomly in the hepatic parenchyma with no fixed relation to portal areas (Fig 1, left). These lesions had some necrosis but less than that seen in herpetic lesions. Instead, they were filled with monocytes and neutrophils (Fig 1, center), confirmed by the demonstration of large amounts of lysozyme in the mononuclear and granular cells (Fig 1, right) and with monoclonal antibody FMC-17 against monocytes-macrophages. Very few T cells were seen in the lesions, using the pan T-cell marker, T11.
Hepatocytes at the edges of the lesions were slightly enlarged without multinucleation. Only a few cells contained intranuclear inclusions, most of which were stellate or cruciate amphophilic bodies (Fig 2, left). Monoclonal antibody to AV was intensely reactive with the nucleus and cytoplasm of cells in and around the lesions but with few cells outside of the lesions (Fig 2, right). There was no reaction with antibody to herpes simplex or CMV except in one instance (to be described later). In one child who died of AV hepatitis, autopsy results three days after biopsy showed progression with a far greater number of punched-out lesions, extensive, almost confluent necrosis, and fewer monocytes and neutrophils. No AV was detected by microscopy outside of the liver. In the second patient, who died 15 days after diagnosis, autopsy results showed extensive hepatic necrosis, but only a minimal amount of viral antigen was demonstrable in liver tissue and no other organ involvement was detected.
Adenovirus was confirmed in the lesions by immunostaining of frozen liver tissue in the four cases tested (Fig 2, right). Viral particles 65 to 90 nm in size were seen in the four cases examined by electron microscopy. Adenovirus and CMV were found together in one lesion. In this instance, characteristic necrotizing lesions were found in which CMV was demonstrable by microscopy and confirmed by immunostaining. Since this type of granulomatous, monocyte-filled lesion is not characteristic of CMV infection, another virus was suspected and AV was detected in the lifted sections. Adenovirus serotype 5 was cultured from liver biopsy specimens in all five patients.
Seventeen patients aged 8 months through 10 years had AV on culture of different body fluids (urine, stool, throat secretions, and/or blood), but without any detectable visceral infection (Table 2). One was a preoperative throat specimen. The other 16 developed infection five days to two years following orthotopic liver transplants. Seven had AV1 isolates, four, AV2; two, AV5; and one, AV7. In three patients the AV isolate was untyped. Nine of 17 had other viral infections (CMV, six; herpes simplex, two; and Epstein-Barr virus, three). Eleven of the 17 had liver biopsies close to the time of the AV isolation, but none showed hepatitis. Eleven of these 17 patients are alive and well. One has chronic rejection; two patients who earlier had Epstein-Barr virus infections developed Epstein-Barr virus-related lymphoproliferative disorders. Three patients died, none as a result of AV infection.
The incidence of AV infections in our patients was 8.4%. This could be an underestimate, because viral cultures were not pursued aggressively in the investigation of a febrile episode earlier on. Also, the use of other media, such as primary or transformed human embryonic kidney cells for viral isolation may have yielded a higher incidence of positive cultures. The same applies to the culturing of liver tissue. The incidence of AV hepatitis was 1.9%, but it is possible that some were missed because it is very difficult to differentiate clinically between rejection and hepatitis, and some patients with hepatitis may not have undergone biopsy. Shields et al10 noted a 4.9% overall incidence of AV infections in 1051 bone marrow recipients of all ages. Visceral infections accounted for 0.95%; two of those had AV hepatitis.
Percutaneous liver biopsy is the most definitive way of diagnosing AV hepatitis. Without this, it may be mistakenly treated as rejection, with detrimental effects. The histological features of AV hepatitis reported in the literature have been those of advanced disease,5,6,14 showing considerable necrosis. The histological appearance we have described is thus characteristic, allowing a presumptive diagnosis to be made on morphological grounds alone. This can be confirmed rapidly and economically by immunoenzyme staining using monoclonal anti-AV antibodies. Electron microscopy is not required routinely. The diagnosis can be made within hours, long before viral cultures of the liver biopsy specimen are definitive, which may take several days.
All hepatitis cases in our series were due to AV5. Experimentally, human A V5 has been shown to cause fulminant hepatitis in newborn hamsters and mice.15,16 Some of the AV hepatitis cases reported in the literature were also caused by AV5.7,10,11 Thus, AV5 may have greater propensity to cause hepatitis than other serotypes, at least in children.
The significance of the AV isolations in group 2 patients is not clear. Even though several of these patients had fevers, it is difficult to attribute them solely to AV infections, as other causes coexisted. It can be argued that some of these are not new AV infections but are episodes of temporary virus shedding following an AV infection in the recent past. This has been shown to happen following enteric and respiratory AV infections in normal children.17
The serotypes isolated in group 2 are similar to the pattern of isolates in the general pediatric population, where AV1 and AV2 accounted for 60% of isolates.2 In contrast to the studies of Shields et al10 in bone marrow transplants, and Horowitz et al,18 in patients with the acquired immunodeficiency syndrome, we did not find any AV35 isolates at all. We do not know at present what determines the onset of hepatitis in a given patient with AV infection.
These infections must have been either exogenously acquired or followed reactivation of latent virus present in the tissues (transplanted organ or recipient’s own) after a remote infection. There was no calendar clustering of cases to suspect a common external source. There is ample evidence to suggest that AV can remain latent in tonsils and adenoids,19 and, latency has been suggested in kidneys also.12 In vitro cultures of human umbilical cord mononuclear leukocytes have shown that AV5 and AV6 can infect and remain in these cells for months, either alone or when the leukocytes have been previously infected by Epstein-Barr virus.20,21 There were three patients in our study who had Epstein-Barr virus and AV infections together, reflecting such an association or a general immunosuppressed state. It has been suggested that the virus may be reactivated from within the recipient’s activated lymphocytes in a rejection process.22 Shields et al23 have shown that reactivation of latent virus in the recipient’s tissue is a strong possibility because in 15 bone marrow recipients with AV infections, 12 had neutralizing antibodies in pre-transplant serum samples. It is not known whether AV infection can initiate allograft rejection, but CMV infections have been implicated in causing allograft rejection.24
Most of the patients with AV hepatitis reported in the literature have died5–7,14,25 with coagulopathy, encephalopathy, and gastrointestinal tract bleeding. The absence of any specific chemotherapeutic agent effective against AV limits treatment options. There are two single case reports of serious AV infections successfully treated, one with thymic humoral factor26 and the other, an AV5 infection, with immune serum globulin containing high titer of neutralizing antibody to AV5.27 Our policy in treating these patients was to decrease the immunosuppression, trying to achieve a delicate balance between treating rejection and infection. Three of our five patients with hepatitis are alive and well at home. One of the patients had very rapid progression to fulminant hepatitis and died in a few days. The other patient who survived for 15 days following the onset of hepatitis had only a minimal amount of virus demonstrable in the liver at the time of autopsy and may have lived had we been able to retransplant the liver. It is noteworthy that the child with the mixed picture of rejection and AV hepatitis did not develop recurrent AV infection in the new allograft after retransplantation.
This work was supported in part by research grants from the Veterans Administration, and project grant AM-29961 from the National Institutes of Health.
The authors are very grateful for the help provided by Richard Debiaso, MS, and Abid Rahman, MS, in the virology laboratory of Children’s Hospital of Pittsburgh.