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Pediatric Acute Severe Hepatitis of Unknown Origin: What is New?

  • Jing Li1,2,
  • Wei Hu2,
  • Ji-Yuan Zhang2 and
  • Fu-Sheng Wang1,2,* 
Journal of Clinical and Translational Hepatology   2022;10(3):509-514

doi: 10.14218/JCTH.2022.00247

Received:

Revised:

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Published online:

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Citation: Li J, Hu W, Zhang JY, Wang FS. Pediatric Acute Severe Hepatitis of Unknown Origin: What is New?J Clin Transl Hepatol. 2022;10(3):509-514. doi: 10.14218/JCTH.2022.00247.

Abstract

Globally, there are emerging cases of acute severe hepatitis of unknown origin in children. These cases have gathered increasing attention, owing to the development of acute liver failure in some cases that resulted in liver transplantation. This review briefly summarizes the outbreak and diagnostic criteria of the disease. We further discuss the possible causes and related mechanisms underlying its occurrence and progression, and analyze the challenges in management. Finally, this review emphasizes patient management in clinical settings and a combination of efforts to unmask the disease.

Keywords

Hepatitis, Children, Diagnostic, Mechanism, Management

Outbreak of acute severe hepatitis of unknown origin in children

On March 31, 2022, five children (aged 3–5 years) in Scotland were the first to be diagnosed with acute severe hepatitis without an identified origin. As of April 5, more than 10 cases of acute severe hepatitis in children under 10 years of age were retrospectively reported in Scotland, with the earliest being January 1, 2022. These emerging cases raised concerns since they outnumbered the annual cases reported in this region of the UK.1 Globally, reports of children with acute hepatitis continue to increase (Fig. 1). As per the latest reports from the World Health Organization (WHO) and European Centre for Disease Prevention and Control (ECDC) on May 18,2,3 the number of cases worldwide has increased to 576 from 28 countries. Among these countries, the UK reported 176 cases and the USA reported 180 cases. In Asia, cases have been reported from Indonesia (21 cases), Israel (12 cases), and Japan (12 cases). The distribution of reported cases is shown in Figure 2.

Timeline of major events in acute severe hepatitis children with unknown origin from March 31 to May 18, 2022.
Fig. 1  Timeline of major events in acute severe hepatitis children with unknown origin from March 31 to May 18, 2022.
Distribution of reported cases with acute severe hepatitis of unknown origin worldwide until May 18, 2022.
Fig. 2  Distribution of reported cases with acute severe hepatitis of unknown origin worldwide until May 18, 2022.

(A) Number of reported cases up to 18th May, 2022; (B) Distribution of diagnosed cases worldwide.

Clinical manifestation and laboratory testing

The clinical characteristics of the reported cases mainly include (1) age at presentation (of 1 month to 16 years), with most affected children under the age of 10 years; (2) a significant elevation of serum alanine aminotransferase (ALT) or aspartate transaminase (AST) >500 U/L; and (3) symptoms including jaundice, nausea, abdominal pain, fatigue, lethargy, and gastrointestinal manifestations, such as diarrhea and vomiting. Fever was reported less frequently; in particular, it was reported in Alabama (5/9 cases) and England (24/81) but not in Scotland. The most important laboratory finding was the absence of known hepatitis viruses (hepatitis A, B, C, D, and E viruses) in any of the reported cases. Preliminary epidemiological data have shown that there is no association between the disease and the use of drugs, exposure to toxins, COVID-19 vaccination, nor environmental factors.2

On April 23, 2022, the WHO issued a communiqué statement that adenovirus infection was detected in at least 74 cases. Among samples from 18 cases analyzed through adenovirus genotyping, adenovirus type 41 was identified. Three separate studies have reported the rate of adenovirus infection, as follows: Alabama (100%, 9/9), England (75.5%, 40/53), and Scotland (38.5%, 5/13) (Table 1).1,4,5 In addition to adenovirus, systemic acute respiratory syndrome (SARS)-coronavirus-2 (CoV-2) monoinfection was detected in 20 cases via real-time PCR testing. Notably, coinfection of adenovirus and SARS-CoV-2 was detected in 19 cases. Among the nine patients in the USA, two recovered after liver transplantation and seven recovered without liver transplantation; there were no reports of mortality. Among the 43 patients in England, 3 had a full recovery after liver transplantation. By May 11, 2022, at least 11 children died outside England, including five children in Indonesia, 5 in the Americas, and 1 in Palestine.2 The latest data jointly released by the WHO and ECDC show that the proportion of diagnosed children with acute liver failure who required liver transplantation was approximately 6%.3

Table 1

Summary of acute severe hepatitis children with unknown origin from the USA, England and Scotland respectively

Alabama, USAEngland, UKScotland, UK
Cases (n)98113
Median age (years)233.9
Female/male7/244/376/7
Liver enzymes, median (range)
  ALT (U/L)1,724 (603–4,696)//
  AST (U/L)1,963 (447–4,000)//
  Total bilirubin (mg/dL)7 (0.23–13.5)//
Clinical manifestations
  Jaundice6/9 (66.7)60/81 (74.1)8/9 (88.9)
  Abdominal pain//7/9 (77.8)
  Vomiting7/9 (77.8)59/81 (72.8)4/4 (100)
  Pale stools/47/81 (58.0)/
  Lethargy/45/81 (55.6)4/4 (100)
  Diarrhea6/9 (66.7)40/81 (49.4)4/4 (100)
  Nausea/32/81 (39.5)6/9 (66.7)
  Fever5/9 (55.6)24/81 (29.6)0/4 (0)
  Upper respiratory symptoms3/9 (33.3)16/81 (19.8)/
  Scleral icterus8/9 (88.9)//
  Hepatomegaly7/9 (77.8)//
  Hepatic encephalopathy1/9 (11.1)//
  Splenomegaly1/9 (11.1)//
Pathogen test (pos/total, %)
  Adenovirus9/9 (100)40/53 (75.5)5/13 (38.5)
  Epstein-Barr virus6/9 (66.7)8/45 (17.8)/
  Enterovirus/Rhinovirus4/8 (50.0)5/20 (25.0)2/13 (15.4)
  Norovirus//2/13 (15.4)
  Cytomegalovirus/3/47 (6.4)1/13 (7.7)
  Metapneumovirus1/8 (12.5)//
  Respiratory syncytial virus1/8 (12.5)2/13 (15.4)/
  Human coronavirus OC431/8 (12.5)//
  Human coronavirus NL63//1/13 (7.7)
  SARS-CoV-20/9 (0)10/61 (16.4)3/13 (23.1)
  Hepatitis A/B/C/E virus0/9 (0)/0/13 (0)
Outcome, number (%)
  Recovered without liver transplantation7/9 (77.8)43/81 (53.1)8/13 (61.5)
  Recovered with liver transplantation and recovered2/9 (22.2)7/81 (8.6)5/13 (38.5)*
  Currently hospitalized or unknown discharge status/31/81 (38.3)/
  Death0/9 (0)0/81 (0)0/13 (0)

In general, epidemiological features revealed that most patients were not vaccinated against SARS-CoV-2. Except for 2 of the 13 patients in Scotland, who had close contact with the other two affected children,1 an obvious epidemiologic association was lacking in most cases reported in the Americas and England.

Differential diagnosis and treatment strategies

Differential diagnosis should be accomplished with the exclusion of other diseases, including (1) hepatophilic viral infections, such as hepatitis A, B, C, D, and E viruses; (2) non-hepatitis infections, such as those caused by rhinovirus, Epstein-Barr virus, cytomegalovirus, human herpes viruses, microvirus B19, and human immunodeficiency virus-1 (HIV-1); (3) non-viral pathogens that cause acute hepatitis, such as meningococcus and leptospira; (4) drugs or toxins, such as azithromycin and erythromycin; (5) immune-mediated liver injury, such as autoimmune liver diseases, hemophagocytic lymph histiocytosis, and gestational alloimmune liver disease; and (6) inherited metabolic liver diseases, such as hepatolenticular degeneration in children older than 5 years and in adolescents.

Children with acute severe hepatitis are at risk of disease exacerbation. Currently, there is a lack of consensus on the treatment regimen for this disease. Dynamically monitoring the biochemical parameters in the blood and clinically assessing the condition of affected children can help physicians assess disease progression promptly to modify the therapeutic strategies as needed.

Among the current treatment strategies, symptomatic therapy, such as the use of hepatoprotective drugs, is experience-based in clinic and needs to be further studied in the acute severe hepatitis with unknown origin. With this approach, in particular, physicians should be cautious when treating severe cases at risk of severe complications, such as hepatic encephalopathy, hepatorenal syndrome, secondary infection, and sepsis. Antiviral therapy should be initiated to control viral replication if the virus is identified. Liver transplantation is recommended in severe cases of acute liver failure. Whether artificial liver supportive therapy can be administered to children requires further study. If immune hyperactivation is involved in disease progression, immunomodulatory therapy, such as glucocorticoid therapy, is worth considering and may be beneficial in reducing liver injury in children.

Disease etiology: induced by pathogens or non-infectious factors?

The primary priority was to identify the cause of acute severe hepatitis in children. Although hepatitis A, B, C, D, and E viruses were excluded, other pathogens or non-infectious factors may have contributed to or resulted in the observed hepatitis cases.

Since adenovirus was most frequently detected in these patients, it is considered a suspected pathogen. Three studies from Scotland, UK and Alabama, USA reported adenovirus positivity rates in children ranging from 39% to 100%.1,4,5 Furthermore, the two cohorts of children (severe acute hepatitis of unknown origin or adenovirus infection) had a similar age range.6 In addition, the England-based patients who received liver transplantation had approximately 12-fold adenovirus DNA levels than those who did not receive liver transplantation.7 However, more robust data are still needed to support this notion. Although more than 25% of children tested positive for adenovirus infection in their respiratory, serum, or stool samples, according to a report from the ECDC,3 there are some concerns with this hypothesis. Adenovirus positivity in throat swab samples was found in 11% of healthy children.8–10 However, acute severe hepatitis induced by adenovirus infection is rarely observed in healthy children. The gold standard method for the diagnosis of adenoviral hepatitis is the detection of adenovirus inclusion bodies in liver biopsy samples.11 However, adenovirus inclusion bodies were not observed in the current study. In addition, a high serum adenoviral load was absent in the reported cases. Furthermore, it is documented that ADV41 infection mainly causes gastrointestinal symptoms, such as diarrhea, and rarely causes acute hepatitis. In clinical settings, 72% of patients with adenoviral hepatitis were mainly infected with strains ADV2 and ADV5. Thus, whether adenovirus infection is the cause of the current disease needs to be further clarified.

SARS-CoV-2 is also considered a suspected (contagious pathogen) contributor. Among the 12 cases reported in Israel, 11 had a history of SARS-CoV-2 infection.12 Studies have shown that viral RNA of SARS-CoV-2 remains in the gastrointestinal tract of affected children longer than in the respiratory tract.13,14 Therefore, the superantigen motif in the spike protein of SARS-CoV-2, structurally similar to staphylococcal enterotoxin B, could trigger broad activation of non-specific T cells, which may lead to a multisystem inflammatory syndrome in children.15–18 Alternatively, similar to patients with HIV-1,19 the children previously infected by SARS-CoV-2 may have a repetitive immune activation caused by the comparatively long-term existence of SARS-CoV-2 in the gastrointestinal tract.20 Under these conditions, children may be prone to infections by other viruses, which would contribute to the development of acute hepatitis. Previous animal studies reported that adenovirus infection significantly enhanced T cell activation mediated by superantigens. This increased the risk of toxic shock with liver damage.21,22 Thus, continuous monitoring of SARS-CoV-2 superantigen is strongly recommended for affected children to clarify whether SARS-CoV-2 superantigen, together with infection with adenovirus or other viruses, caused the disease.

In addition to the above-mentioned viral infection, bacterial and/or fungal infection may induce hepatitis, particularly under conditions of systematic infection. However, there is no clinical evidence to date that supports this. Other non-infectious factors may be responsible for the incidence or contribute to the progression of acute severe hepatitis of unknown etiology, including genetic susceptibility, unknown toxin exposure, hepatotoxic drugs, or environmental exposure factors. Unlike highly transmissible viral infections, these factors are not contagious and cannot induce a global pandemic. Thus, there are no concerns regarding biosafety issues.

Challenges and perspectives

During the last several months, there have been increasing reports not only from the literature, WHO, and Centers for Disease Control (CDCs) of different countries worldwide but also from social/public media and many We-Media, which may overstate the risk of the disease and its potential for a global pandemic. Therefore, hepatologists should pay attention to the potential biosafety issues involved in this disease.

Some challenges must be addressed immediately. It is crucial to document unmet issues of acute severe hepatitis of unknown etiologies in children. Further epidemiological studies and whole-genome sequencing of biological samples may help identify the pathogen responsible for the disease. Close collaboration between physicians and scientists is critical to conduct basic, translational, and clinical studies to highlight epidemiology. Rapid diagnosis in potential cases is necessary for better disease management. Furthermore, it is necessary to clarify viral, immunological, and pathological mechanisms underlying acute severe hepatitis. In summary, complete control of the disease may require significant public health and medical efforts.

It may be helpful to consider the current progress in the management of adults with acute severe hepatitis when taking care of affected children. Although there are few reports, acute severe hepatitis of unknown origin was previously investigated in adult patients. Cytopenia is one of the most frequently observed clinical features. Reportedly, 49% of adult patients required liver transplantation, and 24% of them died from acute liver failure.23 Steroid treatment may be effective for some patients. The characteristics of pediatric patients are distinct from adult patients, suggesting that clinical experience drawn from adult patients can only be used as a general reference for pediatric patients. There is an urgent need to develop effective treatment strategies for pediatric patients.

As recently recommended by the WHO, acute severe hepatitis of unknown origin in children should be actively monitored and extensively studied worldwide. Therefore, it is also necessary to investigate and assess the risk of the disease and disease progression. Moreover, routine preventive measures, such as careful hand-washing and mask-wearing, should be advocated for all children and their caregivers to avoid potential pathogenic infections. Furthermore, professional training and awareness among pediatricians and other clinicians along with development of disease management guidelines are crucial to improve the diagnosis and treatment of acute severe hepatitis of unknown origin in children.

Abbreviations

ECDC: 

European Centre for Disease Prevention and Control

SARS-CoV-2: 

severe acute respiratory syndrome coronavirus 2

WHO: 

World Health Organization

Declarations

Funding

Innovation Groups of the National Natural Science Foundation of China (No. 81721002), China National Natural Science Foundation (No. 82130019)

Conflict of interest

FSW has been an executive associate editor of Journal of Clinical and Translational Hepatology since 2022. The other authors have no conflict of interests related to this publication.

Authors’ contributions

Study concept and design (FSW, JL and JYZ), literature search and drafting of the manuscript (JL, WH and JY), critical revision of manuscript for important intellectual content, senior authorship guidance and supervision (FSW). All authors agreed with the final version of the manuscript.

References

  1. Marsh K, Tayler R, Pollock L, Roy K, Lakha F, Ho A, et al. Investigation into cases of hepatitis of unknown aetiology among young children, Scotland, 1 January 2022 to 12 April 2022. Euro Surveill 2022;27(15):2200318 View Article PubMed/NCBI
  2. European centre for disease prevention and control. Epidemiological update: Hepatitis of unknown aetiology in children. Available from: https://www.Ecdc.Europa.Eu/en/news-events/epidemiological-update-hepatitis-unknown-aetiology-children View Article PubMed/NCBI
  3. World Health Organization 2022. European Centre for Disease Prevention and Control 2022. Joint ECDC-WHO Regional Office for Europe Hepatitis of Unknown Origin in Children Surveillance Bulletin. Available from: https://cdn.ecdc.europa.eu/novhep-surveillance/ View Article PubMed/NCBI
  4. UK Health Security Agency Technical briefing: Increase in hepatitis (liver inflammation) cases in children under investigation, Version 2.0; May 6 2022. Available from: https://www.gov.uk/government/news/increase-in-hepatitis-liver-inflammation-cases-in-children-under-investigation View Article PubMed/NCBI
  5. Baker JM, Buchfellner M, Britt W, Sanchez V, Potter JL, Ingram LA, et al. Acute Hepatitis and Adenovirus Infection Among Children - Alabama, October 2021-February 2022. MMWR Morb Mortal Wkly Rep 2022;71(18):638-640 View Article PubMed/NCBI
  6. Essa SG, Zaki MES, Elmansoury EA, Hassan RH, El Kheir NYA. Molecular Study of Adenovirus Genotypes 40 and 41 in Children with Acute Gastroenteritis. Infect Disord Drug Targets 2022;22:e090522204400 View Article PubMed/NCBI
  7. UK health security agency technical briefing: adenovirus DNA levels in Investigation into acute hepatitis of unknown aetiology in children in england, version 1.0. Gov-12076; April 25 2022. Available from: https://www.Gov.Uk/government/publications/acute-hepatitis-technicalbriefing View Article PubMed/NCBI
  8. Song E, Wang H, Kajon AE, Salamon D, Dong S, Ramilo O, et al. Diagnosis of Pediatric Acute Adenovirus Infections: Is a Positive PCR Sufficient?. Pediatr Infect Dis J 2016;35(8):827-834 View Article PubMed/NCBI
  9. Djeneba O, Damintoti K, Denise I, Christelle NW, Virgilio P, Adrien B, et al. Prevalence of rotavirus, adenovirus and enteric parasites among pediatric patients attending Saint Camille Medical Centre in Ouagadougou. Pak J Biol Sci 2007;10(23):4266-4270 View Article PubMed/NCBI
  10. Leen AM, Rooney CM. Adenovirus as an emerging pathogen in immunocompromised patients. Br J Haematol 2005;128(2):135-144 View Article PubMed/NCBI
  11. Schaberg KB, Kambham N, Sibley RK, Higgins JPT. Adenovirus Hepatitis: Clinicopathologic Analysis of 12 Consecutive Cases From a Single Institution. Am J Surg Pathol 2017;41(6):810-819 View Article PubMed/NCBI
  12. Israel News. Everything You Need to Know About the Hepatitis Outbreak Among Children. Available from: https://www.haaretz.com/israel-news/everything-you-need-to-know-about-the-hepatitis-outbreak-among-children-1.10754895 View Article PubMed/NCBI
  13. Du W, Yu J, Liu X, Chen H, Lin L, Li Q. Persistence of SARS-CoV-2 virus RNA in feces: A case series of children. J Infect Public Health 2020;13(7):926-931 View Article PubMed/NCBI
  14. Xing YH, Ni W, Wu Q, Li WJ, Li GJ, Wang WD, et al. Prolonged viral shedding in feces of pediatric patients with coronavirus disease 2019. J Microbiol Immunol Infect 2020;53(3):473-480 View Article PubMed/NCBI
  15. Noval Rivas M, Porritt RA, Cheng MH, Bahar I, Arditi M. COVID-19-associated multisystem inflammatory syndrome in children (MIS-C): A novel disease that mimics toxic shock syndrome-the superantigen hypothesis. J Allergy Clin Immunol 2021;147(1):57-59 View Article PubMed/NCBI
  16. Brown M, Bhardwaj N. Super(antigen) target for SARS-CoV-2. Nat Rev Immunol 2021;21(2):72 View Article PubMed/NCBI
  17. Ramaswamy A, Brodsky NN, Sumida TS, Comi M, Asashima H, Hoehn KB, et al. Immune dysregulation and autoreactivity correlate with disease severity in SARS-CoV-2-associated multisystem inflammatory syndrome in children. Immunity 2021;54(5):1083-1095.e7 View Article PubMed/NCBI
  18. Sacco K, Castagnoli R, Vakkilainen S, Liu C, Delmonte OM, Oguz C, et al. Immunopathological signatures in multisystem inflammatory syndrome in children and pediatric COVID-19. Nat Med 2022;28(5):1050-1062 View Article PubMed/NCBI
  19. Xia P, Xing XD, Yang CX, Liao XJ, Liu FH, Huang HH, et al. Activation-induced pyroptosis contributes to the loss of MAIT cells in chronic HIV-1 infected patients. Mil Med Res 2022;9(1):24 View Article PubMed/NCBI
  20. Brodin P. SARS-CoV-2 infections in children: Understanding diverse outcomes. Immunity 2022;55(2):201-209 View Article PubMed/NCBI
  21. Brodin P, Arditi M. Severe acute hepatitis in children: investigate SARS-CoV-2 superantigens. Lancet Gastroenterol Hepatol 2022 View Article PubMed/NCBI
  22. Yarovinsky TO, Mohning MP, Bradford MA, Monick MM, Hunninghake GW. Increased sensitivity to staphylococcal enterotoxin B following adenoviral infection. Infect Immun 2005;73(6):3375-3384 View Article PubMed/NCBI
  23. Muller R, Briantais A, Faucher B, Borentain P, Nafati C, Blasco V, et al. Acute severe hepatitis in adult-onset Still’s disease: case report and comprehensive review of a life-threatening manifestation. Clin Rheumatol 2021;40(6):2467-2476 View Article PubMed/NCBI