0% found this document useful (0 votes)
66 views19 pages

Brief Reports

This international survey of healthcare professionals found variations in COVID-19 vaccination policies for children with a history of multisystem inflammatory syndrome in children (MIS-C). The survey received complete responses from 83 professionals in 32 countries. They reported 273 children with a history of MIS-C received COVID-19 vaccines, and did not observe any relapses of MIS-C or other severe inflammatory side effects after vaccination. While COVID-19 vaccines are generally well-tolerated, rare inflammatory events have been documented after vaccination in other populations. The optimal vaccination strategy for children with a history of MIS-C remains unclear.

Uploaded by

dery serna
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
0% found this document useful (0 votes)
66 views19 pages

Brief Reports

This international survey of healthcare professionals found variations in COVID-19 vaccination policies for children with a history of multisystem inflammatory syndrome in children (MIS-C). The survey received complete responses from 83 professionals in 32 countries. They reported 273 children with a history of MIS-C received COVID-19 vaccines, and did not observe any relapses of MIS-C or other severe inflammatory side effects after vaccination. While COVID-19 vaccines are generally well-tolerated, rare inflammatory events have been documented after vaccination in other populations. The optimal vaccination strategy for children with a history of MIS-C remains unclear.

Uploaded by

dery serna
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
You are on page 1/ 19

BRIEF REPORTS

Severe Acute Respiratory Syndrome Coronavirus 2 Vaccination in Children


with a History of Multisystem Inflammatory Syndrome in Children:
An International Survey
Levi Hoste, MD1,2, MIS-C researchers*, Antoni Soriano-Arandes, MD, PhD3, Emilie Pauline Buddingh, MD, PhD4,
Elizabeth Whittaker, MD, PhD5,6, Alexandre Belot, MD, PhD7, Rolando Ulloa-Gutierrez, MD8, Peter Olbrich, MD, PhD9,10,†,
and Filomeen Haerynck, MD, PhD1,2,†

The optimal severe acute respiratory syndrome coronavirus 2 vaccine strategy for patients with a history of multi-
system inflammatory syndrome in children (MIS-C) is unclear. We performed an international survey (32 countries)
and found substantial variations in vaccine policies. Respondents did not report relapses of MIS-C or other severe
inflammatory side effects after severe acute respiratory syndrome coronavirus 2 vaccination in 273 patients with a
history of MIS-C. (J Pediatr 2022;248:114-8).

I
n approximately 1 in 3000 to 5000 severe acute respiratory SARS-CoV-2 spike, S1, and nucleocapsid antigens have
syndrome coronavirus 2 (SARS-CoV-2) infections, multi- been detected in plasma of patients with MIS-C.14
system inflammatory syndrome in children (MIS-C) oc- Currently approved pediatric vaccines against coronavirus
curs with a severe and potentially life-threatening disease disease 2019 are mRNA-based and encode for the SARS-
course (1%-2% mortality).1-3 MIS-C primarily affects previ- CoV-2 spike protein.15-17 SARS-CoV-2 vaccination generally
ously healthy children between 6 and 10 years of age.2,3 Be- is well tolerated, even in young children.18 Nevertheless, rare
sides high-grade fever, the clinical spectrum includes but severe inflammatory events have been documented after
gastrointestinal, cardiovascular, dermatologic, and neuro- SARS-CoV-2 vaccination, such as myocarditis in young
logic symptoms.3,4 In addition to supportive care, most pa- (male) adults,19 or broader multisystem inflammation
tients are treated with immunomodulatory therapies, (MIS after SARS-CoV-2 vaccination) in adolescents or
including 1 or more of intravenous immunoglobulin, sys- adults.20-26 In children who previously experienced MIS-C,
temic corticosteroid, and a biologic response–modifying re-exposure to the viral protein could trigger a relapse of hy-
agent.5 Pediatric SARS-CoV-2–related hospitalizations perinflammation, especially with a presumed superantigen
increased during the more recent omicron surge, both in underlying the pathophysiology of MIS-C. To date, limited
relative (18% of hospitalizations in South Africa were chil- data are available in children receiving SARS-CoV-2 vaccina-
dren)6 and absolute numbers (4-5 times as many children tion after MIS-C. We performed an international survey
hospitalized in the US compared with delta surge).7 To
date, it is unclear how the incidence of MIS-C evolves with
different SARS-CoV-2 variants, although a recent preprint
From the 1Primary Immune Deficiency Research Laboratory, Department of Internal
suggests a lower risk for MIS-C when delta and omicron Diseases and Pediatrics, Centre for Primary Immunodeficiency Ghent, Jeffrey Modell
were dominant compared with alpha lineage.8 Diagnosis and Research Centre, and 2Department of Internal Medicine and
Pediatrics, Division of Pediatric Pulmonology, Infectious Diseases and Inborn Errors
Although the pathophysiology of MIS-C remains enig- of Immunity, Ghent University Hospital, Ghent, Belgium; 3Pediatric Infectious
Diseases and Immunodeficiencies Unit, Hospital Universitari Vall d’Hebron (HUVH),
matic, data show activation of oligoclonally expanded T lym- Barcelona, Spain; 4Department of Pediatrics, Leiden University Medical Centre,
Leiden, The Netherlands; 5Paediatric Infectious Diseases, Imperial College
phocytes, reminiscent of disease driven by superantigen Healthcare NHS Trust, London, United Kingdom; 6Section of Paediatric Infectious
exposure such as in toxic shock syndrome. In MIS-C, howev- Diseases, Imperial College, London, United Kingdom; 7Pediatric Nephrology
Rheumatology and Dermatology, CHU Lyon, Lyon, France; 8Servicio de Infectologıa
er, upregulated T lymphocytes associated with MIS-C harbor Pediatrica, Hospital Nacional de Nin~os “Dr Carlos Sa enz Herrera,” Centro de
Ciencias Me dicas, Caja Costarricense de Seguro Social (C.C.S.S.), San Jose , Costa
the TRBV11-2 gene, encoding for the T-cell receptor Vb 21.3, 9
Rica; Pediatric Infectious Diseases, Rheumatology and Immunology Unit, Hospital

which appears to be a highly sensitive and specific feature.9-12 Universitario Virgen del Rocıo, Instituto de Biomedicina de Sevilla, IBiS/Universidad
de Sevilla/CSIC, Red de Investigacio  n Traslacional en Infectologıa Pedia
trica RITIP,
Although the exact source of superantigen in MIS-C remains Sevilla, Spain; and 10Departamento de Farmacologıa, Pediatrıa y Radiologıa,
Facultad de Medicina, Universidad de Sevilla, Spain
unknown, persistence of viral exposure is one of the possibil- *List of MIS-C researchers is available at www.jpeds.com (Appendix 1).
ities, given that widespread replication of SARS-CoV-2 has †Contributed equally.

been demonstrated in deceased patients with MIS-C13 and L.H. was funded by the VIB Grand Challenge Programs and FWO-TBM (T004721N).
F.H. is supported by Ghent University research grant (BOF-UGent), VIB Grand
Challenges Programs, and the Jeffrey Modell Foundation. A.S.-A. is supported by
the Departments of Health and Education of the Government of Catalonia (Spain) for
the coronavirus disease 2019 Sentinel School Network project. P.O. has received
s, JR18/00042),
funding by the Instituto de Salud Carlos III (Contrato Juan Rode
AE Adverse event
Madrid, Spain. The authors declare no conflicts of interest.
MIS-C Multisystem inflammatory syndrome in children
SARS-CoV-2 Severe acute respiratory syndrome coronavirus 2 0022-3476/$ - see front matter. ª 2022 Elsevier Inc. All rights reserved.
https://doi.org/10.1016/j.jpeds.2022.05.028

114
Volume 248  September 2022

among health care professionals to assess experience with excluded after personal communication with the involved
tolerability of SARS-CoV-2 vaccine in children with a history respondents. Given the study design, overall survey
of MIS-C. response rates and subsequently any comparisons between
survey respondents with nonrespondents could not be
Methods performed. On an individual patient level, no identifiable
information was collected. Data were collected from
Our cross-sectional electronic survey (Appendix 2; available November 1, 2021, to December 15, 2021.
at www.jpeds.com) was composed of 24 questions covering
vaccination policies used for children with previous MIS-C
(local, regional, and/or national guidelines); number of
children with a history of MIS-C who were or were not Results
(yet) vaccinated against SARS-CoV-2; and identification of
uncommon adverse events (AEs), codified as possible, Health care professionals (n = 132) involved in the care of pa-
probable, or certain, occurring after SARS-CoV-2 tients with MIS-C initiated the survey. After excluding incom-
vaccination in these children. Respondents were asked to plete entries, we collected complete data from 83 health care
specify whether the entered cases were counted accurately professionals from 32 different countries (Figure 1). Most
(eg, registered as cases) or as estimated numbers. The respondents were clinicians (79/83) and/or clinical
survey link was distributed globally through personal researchers (21/83). Medical specialties included pediatrics
communication by the authors and through email (53/83), pediatric infectious diseases (23/83), cardiology (13/
invitations by multiple professional (inter)national societies 83), immunology (8/83), intensive care and emergency
of pediatrics, infectious diseases, intensive care medicine, medicine (8/83), rheumatology (7/83), and dermatology (1/
inborn errors of immunity, Kawasaki disease/MIS-C 83). Four entries were excluded because of probable or
networks, and clinical trials networks. Participants also confirmed overlapping data. After we excluded these cases,
were asked to distribute the survey invitation to other information from 5673 patients with MIS-C was analyzed
colleagues involved in MIS-C care. The professional (Figure 2). In total, 3465 of these cases were accurately
background of respondents was evaluated to confirm counted and 2208 were reported as estimated case numbers
relevant roles in care and/or policymaking regarding of patients with MIS-C; 44% of the patients had been
patients with MIS-C. IP addresses were verified to ensure admitted to intensive care units during their MIS-C episode.
the uniqueness of each participant. Possible overlapping Of the eligible cohort only 15.6% (273/1750) were
data (eg, national data that included regional counts) were confirmed to have been vaccinated (24.0% [420/1750]).

Figure 1. World map with countries colored that are represented in the dataset. For each country, the number of respondents (n)
is mentioned as well as the number of patients with MIS-C who were reported. Map created by mapchart.net.

Severe Acute Respiratory Syndrome Coronavirus 2 Vaccination in Children with a History of Multisystem 115
Inflammatory Syndrome in Children: An International Survey
THE JOURNAL OF PEDIATRICS  www.jpeds.com Volume 248

well as safety concerns (9/14). Furthermore, 9 participants


stated deviation from the standard vaccine regimen for these
children compared with previously healthy children without
MIS-C or SARS-CoV-2 infection. Recommendations
included a minimal interval between MIS-C and administra-
tion of the first vaccine dose ranging from 3 months (respon-
dents from Italy, Spain, Sweden, Turkey, United Kingdom,
Uruguay, and US) up to 6 months (The Netherlands, United
Kingdom). Some respondents declared intent to administer
only 1 dose instead of the typical 2-dose regimen (Italy,
Spain, and Switzerland).
Most children with previous MIS-C were vaccinated in
the same locations as healthy children according to local
health authority guidelines, such as vaccination centers or
schools (n = 45 respondents), hospitals without admission
(n = 3 from India, Italy and Turkey), or hospitals with
admission (n = 13 from Belgium, South Korea, Colombia,
Indonesia, Spain, Turkey, India, Italy, US). Only 1 respon-
dent from Italy declared that vaccination in a hospital
without admission was a specific procedure for MIS-C not
applying to healthy children.

Tolerability of SARS-CoV-2 Vaccine


Most respondents (54 of 65 entries without contraindication
for vaccination) could not provide specific data on mild or
moderate AE, either because there was lack of formal registra-
tion and/or that respondents were not at all confronted with
Figure 2. Flowchart representing the selection process of these specific AE in patients. Of registered data, mild or mod-
included entries, number of patients with MIS-C reported, and erate AE was reported to a variable extent, including both
their eligibility for COVID-19 vaccination. COVID-19, corona- localized reactions (swelling, redness, pain) and systemic re-
virus disease 2019. sponses (fever, chills, nausea, fatigue, headache, lymphade-
nopathy). As such, frequencies of AEs for individual entries
ranged from 0 to 100% of patients, although importantly,
Patients Who Received the SARS-CoV-2 Vaccine all mild or moderate AEs disappeared after 1-3 days without
As stated by the participants at the time of the survey, 1750 requiring specific interventions. One 13-year-old male recip-
patients with MIS-C (30.8% of the study cohort) were eligible ient was reported with acute-onset facial nerve palsy (Bell’s
by age, vaccine availability, and time since the episode of palsy) 1 week after his second BNT162b2 (Pfizer-BioNTech)
MIS-C for vaccination. In total, 273 (15.6% of eligible pa- vaccine. He was hospitalized and given methylprednisolone
tients) were confirmed to have been vaccinated at the time (40 mg/d) and recovered without sequelae. No other severe
of the survey. For an additional 420 cases (24.0% of eligible AE was reported by the participants. Importantly, no MIS-
patients), respondents assumed vaccine administration based C relapse or any other inflammatory conditions were re-
on the absence of formal contraindication, although no regis- ported after vaccination.
tration or follow-up was performed. This included 81 accu-
rately counted cases and 339 based on estimate numbers. Discussion

Policy and Practice The survey documents heterogeneity of vaccine policy as well
Fourteen of 79 (17.7%) respondents from Belgium, France, as limited data on vaccination after recovery from MIS-C.
India, Italy, Mexico, Pakistan, Turkey, and the US declared Our data suggest that vaccine recommendations or their un-
MIS-C as a contraindication for SARS-CoV-2 vaccination derstanding or both in the context of MIS-C not only differ
at the time of the survey, accounting for 1144 patients between continents and health care systems but also within
(20.2% of the cohort). Of note, not all respondents from countries. Potential harms and benefits of SARS-CoV-2
the same country declared MIS-C as a contraindication (eg, vaccination in children with a history of MIS-C may be
Belgium 7 of 12 respondents, Italy 1/6, Turkey 1/5, US 1/ weighted differently in each setting. Individual choices or
7), suggesting heterogeneous policies or their knowledge on concerns regarding vaccine safety also might exist. Although
a national level. The participants affirmed that vaccination SARS-CoV-2 vaccination was not contraindicated in patients
was contraindicated in their settings due to recommenda- according to the Centers for Disease Control and Prevention
tions of national or regional guidelines (9/14 regions) as guidelines, we observed a heterogeneous advice within
116 Hoste et al
September 2022 BRIEF REPORTS

respondents from the US.27 Although in most countries AEs with MIS-C worldwide who chose to participate and should
of vaccines and drugs are registered centrally by health care be interpreted as such. n
agencies, the rarity of MIS-C and the absence of registries
documenting follow up of vaccination episodes in affected The authors express their sincere gratitude to all collaborating partners,
patients leads to a lack of specific knowledge regarding toler- including Chiara Biazzo, for the relevant literature search. MIS-C re-
ability of SARS-CoV-2 vaccination in these children. searchers who provided data for their hospital (network), region, or
country are listed in Appendix 1.
We found that in most regions around the world, MIS-C is
not considered a contraindication for SARS-CoV-2 vaccina- Submitted for publication Feb 11, 2022; last revision received Apr 25, 2022;
tion. In addition, respondents stated that 273 patients effec- accepted May 16, 2022.
tively received at least 1 dose of SARS-CoV-2 vaccine after Reprint requests: Filomeen Haerynck, MD, PhD, Department of Pediatric
MIS-C. There was no overt experience of increased frequency Pulmonology, Infectious Diseases and Immunology, Ghent University
Hospital, Corneel Heymanslaan 10, Ghent, Belgium. E-mail: filomeen.
or severity of AE and no case of MIS-C relapse or other in- [email protected]
flammatory conditions after vaccination Our observations
are consistent with the overall good safety profile of SARS-
CoV-2 vaccines in healthy children. SARS-CoV-2 vaccina- References
tion is associated with a reduced risk of development of
MIS-C after infection.28,29 It should be noted that Bell’s palsy 1. Belot A, Antona D, Renolleau S, Javouhey E, Hentgen V, Angoulvant F,
was reported as a severe AE in 1 patient30 and generally is et al. SARS-CoV-2-related paediatric inflammatory multisystem syn-
reversible.31 drome, an epidemiological study, France, 1 March to 17 May 2020.
Eurosurveillance 2020;25:2001010. https://doi.org/10.2807/1560-7917.
Administration of a SARS-CoV-2 vaccine after MIS-C ES.2020.25.22.2001010/CITE/PLAINTEXT
was assessed by 20% of participants as contraindicated. 2. Payne AB, Gilani Z, Godfred-Cato S, Belay ED, Feldstein LR, Patel MM,
Furthermore, a substantial number of patients with MIS- et al. Incidence of multisystem inflammatory syndrome in children among
C, even if already eligible for vaccination (30% of the US persons infected with SARS-CoV-2. JAMA Netw Open 2021;4:
cohort), had not been vaccinated or were possibly vacci- e2116420. https://doi.org/10.1001/JAMANETWORKOPEN.2021.16420
3. Hoste L, Van Paemel R, Haerynck F. Multisystem inflammatory syn-
nated, and 60.4% were not. In addition, some respondents drome in children related to COVID-19: a systematic review. Eur J Pe-
declared to propose longer intervals between MIS-C and diatr 2021;180:2019-34. https://doi.org/10.1007/s00431-021-03993-5
vaccination or different dosing schedules than for previ- 4. Feldstein LR, Rose EB, Horwitz SM, Collins JP, Newhams MM,
ously healthy children, potentially exposing patients with Son MBF, et al. Multisystem inflammatory syndrome in U.S. children
MIS-C to a greater risk of reinfection. More detailed infor- and adolescents. N Engl J Med 2020;383:334-46. https://doi.org/10.
1056/NEJMoa2021680
mation on safety of delayed vaccination or 1- vs 2-dose 5. McArdle AJ, Vito O, Patel H, Seaby EG, Shah P, Wilson C, et al. Treat-
vaccination will be of value to define the optimal vaccine ment of multisystem inflammatory syndrome in children. N Engl J Med
strategy for this specific group of patients. it will be of inter- 2021;385:11-22. https://doi.org/10.1056/NEJMoa2102968
est to document whether occurrence of MIS-C is limited to 6. Cloete J, Kruger A, Masha M, du Plessis NM, Mawela D, Tshukudu M,
primary exposure to SARS-CoV-2 or if MIS-C, and with et al. Paediatric hospitalisations due to COVID-19 during the first SARS-
CoV-2 omicron (B.1.1.529) variant wave in South Africa: a multicentre
what frequency, follows reinfection.32 observational study. Lancet Child Adolesc Health 2022;6:294-302.
This analysis is limited by the temporary nature of its data, https://doi.org/10.1016/S2352-4642(22)00027-X
especially in the midst of an evolving pandemic and vaccine 7. Marks KJ, Whitaker M, Anglin O, Milucky J, Patel K, Pham H, et al. Hos-
policies. When this survey was initiated, SARS-CoV-2 vac- pitalizations of children and adolescents with laboratory-confirmed
COVID-19—COVID-NET, 14 States, July 2021–January 2022.
cines were not yet universally accessible for children 5-
MMWR Morb Mortal Wkly Rep 2022;71:271-8. https://doi.org/10.
11 years of age, who represented a substantial proportion 15585/mmwr.mm7107e4
of patients with MIS-C.3 The systematic and prospective 8. Cohen JM, Carter MJ, Cheung CR, Ladhani S , Group EP-TS. Lower risk
collection of additional safety data on younger patients of multisystem inflammatory syndrome in children (MIS-C) with the
with MIS-C is important to either support or adjust conclu- Delta and Omicron variants of SARS-CoV-2. MedRxiv 2022;2022.
sions beyond the current context of predominantly 03.13.22272267.
9. Porritt RA, Paschold L, Noval Rivas M, Cheng MH, Yonker LM,
adolescent patients with MIS-C receiving the BNT162b2 Chandnani H, et al. HLA class I-associated expansion of TRBV11-2 T
(Pfizer-BioNTech) vaccine. A major limitation of the study cells in multisystem inflammatory syndrome in children. J Clin Invest
design is that in only 273 cases vaccine administration has 2021;131:e146614. https://doi.org/10.1172/jci146614
been confirmed, with a potential bias related to recall or noti- 10. Ramaswamy A, Brodsky NN, Sumida TS, Comi M, Asashima H,
fication of AEs. It seems unlikely, however, that attending Hoehn KB, et al. Immune dysregulation and autoreactivity correlate
with disease severity in SARS-CoV-2–associated multisystem inflamma-
physicians or health care providers would not have been noti- tory syndrome in children. Immunity 2021;54:1083-95.e7. https://doi.
fied of important inflammatory complications or MIS-C re- org/10.1016/j.immuni.2021.04.003
lapses. We did not collect individual data on patients, so 11. Moreews M, Le Gouge K, Khaldi-Plassart S, Pescarmona R, Mathieu A-
information on the demography of those vaccinated, the L, Malcus C, et al. Polyclonal expansion of TCR Vbeta 21.3+ CD4+ and
number of doses administered, or the interval between CD8+ T cells is a hallmark of multisystem inflammatory syndrome in
children. Sci Immunol 2021;6:eabh1516. https://doi.org/10.1126/sciim
MIS-C and SARS-CoV-2 vaccination was not documented. munol.abh1516
Finally, data represent a convenience sample supplied by 12. Hoste L, Roels L, Naesens L, Bosteels V, Vanhee S, Dupont S, et al.
numerous professionals involved with the care of patients TIM3+ TRBV11-2 T cells and IFNg signature in patrolling monocytes

Severe Acute Respiratory Syndrome Coronavirus 2 Vaccination in Children with a History of Multisystem 117
Inflammatory Syndrome in Children: An International Survey
THE JOURNAL OF PEDIATRICS  www.jpeds.com Volume 248

and CD16+ NK cells delineate MIS-C. J Exp Med 2022;219:e20211381. literature review. J Korean Med Sci 2021;36:e312. https://doi.org/10.
https://doi.org/10.1084/JEM.20211381 3346/JKMS.2021.36.E312
13. Duarte-Neto AN, Caldini EG, Gomes-Gouv^ea MS, Kanamura CT, de Al- 24. Stappers S, Ceuleers B, Van Brusselen D, Willems P, de Tavernier B,
meida Monteiro RA, Ferranti JF, et al. An autopsy study of the spectrum Verlinden A. A case of multisystem inflammatory syndrome (MIS-A)
of severe COVID-19 in children: from SARS to different phenotypes of in an adult woman 18 days after COVID-19 vaccination. Acta Clin
MIS-C. EClinicalMedicine 2021;35:100850. https://doi.org/10.1016/j. Belg 2021:1-6. https://doi.org/10.1080/17843286.2021.1977899
eclinm.2021.100850 25. Baicus C, Delcea C, Pinte L, Dan GA. Hyper-inflammation after COVID-
14. Yonker LM, Gilboa T, Ogata AF, Senussi Y, Lazarovits R, Boribong BP, 19 mARN vaccination: at the crossroads of multisystem inflammatory
et al. Multisystem inflammatory syndrome in children is driven by disease and adult-onset Still’s disease. Does terminology matter? Rom
zonulin-dependent loss of gut mucosal barrier. J Clin Invest 2021;131: J Intern Med 2022;60:3-5. https://doi.org/10.2478/RJIM-2021-0035
e149633. https://doi.org/10.1172/JCI149633 26. Ouldali N, Bagheri H, Salvo F, Antona D, Pariente A, Leblanc C, et al.
15. Walter EB, Talaat KR, Sabharwal C, Gurtman A, Lockhart S, Paulsen GC, Multisystemic inflammatory syndrome following COVID-19 mRNA
et al. Evaluation of the BNT162b2 Covid-19 vaccine in children 5 to 11 vaccine in children: a national post-authorization pharmacovigilance
years of age. N Engl J Med 2022;386:35-46. https://doi.org/10.1056/NEJ- study. Lancet Reg Health Eur 2022;17. https://doi.org/10.1016/j.
MOA2116298/ lanepe.2022.100393
16. Frenck RW, Klein NP, Kitchin N, Gurtman A, Absalon J, Lockhart S, 27. Interim Clinical Considerations for Use of COVID-19 Vaccines
et al. Safety, immunogenicity, and efficacy of the BNT162b2 Covid-19 Currently Approved or Authorized in the United States [homepage on
vaccine in adolescents. N Engl J Med 2021;385:239-50. https://doi.org/ the Internet]. Centers for Disease Control and Prevention. 2022. Ac-
10.1056/NEJMOA2107456/ cessed April 7, 2022. https://www.cdc.gov/vaccines/covid-19/clinical-
17. Ali K, Berman G, Zhou H, Deng W, Faughnan V, Coronado-Voges M, considerations/interim-considerations-us.html
et al. Evaluation of mRNA-1273 SARS-CoV-2 vaccine in adolescents. 28. Levy M, Recher M, Hubert H, Javouhey E, Flechelles O, Leteurtre S, et al.
N Engl J Med 2021;385:2241-51. https://doi.org/10.1056/NEJMOA Multisystem inflammatory syndrome in children by COVID-19 vaccina-
2109522/ tion status of adolescents in France. JAMA 2022;327:281-3. https://doi.
18. Zimmermann P, Pittet LF, Finn A, Pollard AJ, Curtis N. Should children org/10.1001/JAMA.2021.23262
be vaccinated against COVID-19? Arch Dis Child 2022;107:e1. https:// 29. Zambrano LD, Newhams MM, Olson SM, Halasa NB, Price AM,
doi.org/10.1136/ARCHDISCHILD-2021-323040 Boom JA, et al. Effectiveness of BNT162b2 (Pfizer-BioNTech) mRNA
19. Witberg G, Barda N, Hoss S, Richter I, Wiessman M, Aviv Y, et al. vaccination against multisystem inflammatory syndrome in children
Myocarditis after Covid-19 vaccination in a large health care organiza- among persons aged 12–18 years—United States, July–December
tion. N Engl J Med 2021;385:2132-9. https://doi.org/10.1056/NEJMO 2021. MMWR Morb Mortal Wkly Rep 2022;71:52-8. https://doi.org/
A2110737/ 10.15585/MMWR.MM7102E1
20. Salzman MB, Huang CW, O’Brien CM, Castillo RD. Multisystem in- 30. Wan EYF, Chui CSL, Lai FTT, Chan EWY, Li X, Yan VKC, et al. Bell’s
flammatory syndrome after SARS-CoV-2 infection and COVID-19 palsy following vaccination with mRNA (BNT162b2) and inactivated
vaccination. Emerg Infect Dis 2021;27:1944-8. https://doi.org/10.3201/ (CoronaVac) SARS-CoV-2 vaccines: a case series and nested case-
EID2707.210594 control study. Lancet Infect Dis 2022;22:64. https://doi.org/10.1016/
21. Grome HN, Threlkeld M, Threlkeld S, Newman C, Martines RB, Rea- S1473-3099(21)00451-5
gan-Steiner S, et al. Fatal multisystem inflammatory syndrome in adult 31. Eviston TJ, Croxson GR, Kennedy PGE, Hadlock T, Krishnan AV. Bell’s
after SARS-CoV-2 natural infection and COVID-19 vaccination. Emerg palsy: aetiology, clinical features and multidisciplinary care. J Neurol
Infect Dis 2021;27:2914-8. https://doi.org/10.3201/EID2711.211612 Neurosurg Psychiatry 2015;86:1356-61. https://doi.org/10.1136/JNNP-
22. Nune A, Iyengar KP, Goddard C, Ahmed AE. Multisystem inflammatory 2014-309563
syndrome in an adult following the SARS-CoV-2 vaccine (MIS-V). BMJ 32. Buddingh EP, Vossen ACTM, Lamb HJ, van der Palen RLF,
Case Rep CP 2021;14:e243888. https://doi.org/10.1136/BCR-2021- Brinkman DMC. Reinfection with severe acute respiratory syndrome co-
243888 ronavirus 2 without recurrence of multisystem inflammatory syndrome
23. Park JW, Yu SN, Chang SH, Ahn YH, Jeon MH. Multisystem inflamma- in children. Pediatr Infect Dis J 2021;40:e491-2. https://doi.org/10.1097/
tory syndrome in an adult after COVID-19 vaccination: a case report and INF.0000000000003280

118 Hoste et al
MIS-C researchers

Individual MIS-C professionals that provided data for their hospital (network), region or country are
listed below.

Belgium: Annick Covents - AZ Nikolaas; Ann Verschelde - AZ Sint-Jan Brugge-Oostende; Jelle


Degraeuwe - AZ Maria Middelares Gent; Amaury Delestienne - Europa hospitals Brussels; Emmi Van
Damme - ZNA Middelheim; Petra Schelstraete, Jef Willems, Evelyn Dhont, Joke Dehoorne, Kristof
Vandekerckhove - Ghent University Hospital; Inge Matthijs - AZ Delta Roeselare; Rik De Wolf - UZ
Brussels; Olga Chatzis - University Hospital St-Luc Brussels; Nele Baeck - AZ Jan Palfijn Ghent;
Marguerite Landsberg - Crèches et libéral Bruxelles; Ann De Guchtenaere - AZ Damiaan Oostende;
Catherine Heijmans - CH Jolimont, La Louvière

Brazil: Almeida Flavia - Santa Casa de São Paulo and Sabara Hospital, Rolando Paternina-De La Ossa -
Clinical Hospital of the School of Medicine at the University of São Paulo, Ribeirão Preto; Aline Islabão
- Hospital da Criança de Brasilia José Alencar

Canada: Nagib Dahdah - CHU Sainte-Justine (University of Montreal), Montreal

Chile: Raul Bustos Betanzo - Sanatorio Aleman Concepción Chile

Colombia: Germán Camacho Moreno - HOMI, Fundación Hospital pediatrico La Misericordia,


Universidad Nacional de Colombia; María Claudia Ortega-López - Hospital Infantil Universitario de San
José, Bogotá

Costa Rica : Rolando Ulloa-Gutierrez - Hospital Nacional de Niños "Dr. Carlos Sáenz Herrera", San José ;
REKAMLATINA Network (Red de Enfermedad de Kawasaki en América Laitina).

Denmark: Trine Mogensen - Aarhus University Hospital, Aarhus

Ecuador: Nelly Chavez - Interhospital, Guayaquil

France: Alexandre Belot, Etienne Javouhey - Hospices Civils de Lyon, Lyon ; Brigitte Bader Meunier,
Sylvain Renolleau, Hopital Necker, Paris ; Isabelle Kone-Paut, Hopital Kremlin Bicètre, Paris ; Veronique
Hentgen, CH de Versaille, Le Chesnay ; Francois Angoulvant, Hopital Robert Debré, Paris ; Xavier Iriart,
Hopital Cardiologique, Bordeaux ; Caroline Ovaert, Hopital de La Timone, Marseille ; Loic de Pontual,
Hopital Jean Verdier, Bondy ; Nina Deschamps, CH de St Malo, St Malo ; Christele Gras-Le Guen, CHU
de Nantes, Nantes

Germany: Markus Hufnagel - University Medical Center Freiburg

Greece: Lampros Fotis - National and Kapodistrian University of Athens; Patra Koletsi - Penteli
Children’s Hospital

Guatemala: Shirley Cuan - Hospital Herrera LLerandi, Guatemala City; Andrea Gatica - Hospitales La
Paz

Honduras : Karla Borjas - IHSS/Hospital Maria

India: Sibabratta Patnaik - Kalinga Institute of Medical Sciences, Bhubaneswar; Chandrika Bhat -
Rainbow Children’s Hospital, Bangalore; Ravindra Pawar - D.Y Patil medical college hospital and
research institute, Kadamwadi, Kolhapur, Maharashtra; Abdul Rauf - Baby Memorial Hospital, Calicut,
Kerala; Vineetranjan Gupta - Asian Institute of medical Sciences, Faridabad; Alpana Mohta - Sardar
Patel Medical College, Bikaner, Rajasthan; Supratim Sen - SRCC Children's Hospital, Mumbai
Indonesia: Nina Dwi Putri - Universitas Indonesia, Cipto Mangunkusumo National Center Hospital,
Jakarta

Iraq: Aso Salih - Sulaimani University

Italy: Riccardo Guanà - Regina Margherita Children's Hospital, Turin; Enza D'Auria - Head Allergy Unit-
Vittore Buzzi Children's Hospital-University of Milan; Buonsenso Danilo - Fondazione Policlinico
Universitario A. Gemelli IRCCS, Rome; Minoia Francesca - Fondazione IRCCS Ca' Granda Ospedale
Maggiore Policlinico, Milan; Luana Nosetti - Pediatric Clinic Insubria University Varese; Gabriele
Simonini - Aou Meyer Firenze

Mexico : Emmanuelle Fernandez - Secretaría de Marina

Pakistan: Indus hospital and health network, Badin, Sindh

Panama: Elizabeth Castaño - Hospital del Niño, Panama

Peru: Elmer Zapata Yarlequé - Hospital Cayetano Heredia and Clinica San Felipe, University Professor
at the Universidad Peruana Cayetano Heredia, Lima

Portugal: Ana Reis-Melo - Centro Hospitalar de São João, Porto

South Africa: Arifa Parker - Stellenbosch University, Cape Town

South Korea: Eun Hwa Choi - Seoul National University Hospital, Seoul; Ji Hee Kwak - Kangbuk Samsung
Hospital, Sungkyunkwan University School of Medicine, Seoul

Spain: García-Salido Alberto - Hospital Infantil Universitario Niño Jesús, Madrid; Marta Aboza Garcia
and Olaf Neth- Virgen del Rocío University Hospital, Sevilla; COPEDICAT research network: Antoni
Soriano-Arandes and Jacques Rivière - Hospital Universitari Vall d'Hebron; Pilar Villalobos - Fundació
Salut Empordà, Figueres; Marc García Lorenzo – Hospital Universitari Sant Joan de Reus, Tarragona;
Anna Gatell - Equip Territorial de Pediatria Garraf-Alt Penedès, Barcelona; Abel Martinez-Mejias -
Consorci Sanitari de Terrassa, Barcelona; Borja Guarch-Ibañez - Hospital Universitari Josep Trueta,
Girona; Carlos Herrero - Hospital de Barcelona, Barcelona; Anton Foguet - Hospital d’Olot i Equip
Pediàtric Territorial Garrotxa i Ripollès, Girona; Fernando Paredes and Núria Visa-Reñé - Hospital
Universitari Arnau de Vilanova, Lleida; Gloria Ruiz - Equip de Pediatria dels Pirineus, Alt Urgell i Pallars,
Lleida; Isabel Aguilar - ABS Sant Boi del Llobregat, Barcelona; Maria Esteller - CAP Aldea-Camarles-
l'Ampolla, Tarragona; Montse Ruiz - Hospital Universitari de Vic, Barcelona; Nuria Lopez - Hospital
Universitari del Mar, Barcelona; Romina Conti - Consorci Corporació Sanitària Parc Taulí de Sabadell,
Barcelona; Rosa Maria Pino - Hospital Universitari Sant Joan de Déu, Esplugues de Llobregat,
Barcelona; Teresa Fenollosa - Gran Sol de Badalona, Barcelona; Emiliano Mora - Hospital Universitari
Mútua de Terrassa, Barcelona; Sonia Brio - Hospital de la Santa Creu I Sant Pau, Barcelona; Maria
Coma, Hospital Universitari Joan XXIII, Tarragona.

Sweden: Petter Brodin - Karolinska Institute, Stockholm

Switzerland: Johannes Trück - University Children's Hospital Zurich, University of Zurich; Géraldine
Blanchard Rohner - Geneva University Hospitals and University of Geneva; Michael Buettcher - Lucerne
Children‘s Hospital

The Netherlands: Emmeline Buddingh, Leids Universitair Medisch Centrum, on behalf of the COPP-
consortium: Leids Universitair Medisch Centrum: Gertjan Lugthart, David Slotboom, Anne Verbeek,
Danielle Brinkman, Petra Hissink Muller, Erik von Asmuth; Erasmus MC: Miriam Mooij, Corinne
Buysse, Rianne Oostenbrink, Pieter Fraaij, Naomi Ketharanathan; AUMC: Simone Hashimoto,
Caroline Brackel, Mariken Gruppen, Taco Kuijpers, Merlijn vd Berg, Martijn vd Kuip, Suzanne
Terheggen-Lagro; Maastricht UMC+: Manouk van der Steen, Michiel Bannier; Universitair Medisch
Centrum Groningen: Liesbeth Scholvinck, Wineke Armbrust, Elizabeth Legger; Albert Schweitzer
Ziekenhuis: Ankie Lebon, Radboud UMC: Koen van Aerde, Ronald Petru, Saskia de Wildt; Amphia
Ziekenhuis: Sanne Hammer; Máxima MC: Lonneke van Onzenoort; Zuyderland Medisch Centrum:
Han Hendriks; Isala: Jolita Bekhof; Spaarne Gasthuis: Marlies van Houten; Bernhoven: Jan van der
Linden; Franciscus Gasthuis & Vlietland: Gerdien Tramper; Maasstad Ziekenhuis: Michael
Groeneweg, Xandra van den Tweel; Hagaziekenhuis (Juliana kinderziekenhuis): Esther Peeters,
Denise Rook, Mirjam van Veen; HMC: Jantien Bolt; Groene Hart Ziekenhuis: Helma van Gameren;
Meander Medisch Centrum: Margot Ernst-Kruis; UMC Utrecht: Joanne Wildenbeest, Joris van
Montfrans, Tom Wolfs, Bas Vastert; Alrijne Ziekenhuis: Anjali Kooter-Bechan; Martini Ziekenhuis:
Arvid Kamps; Bravis ziekenhuis: Stephanie de Crom, Christiaan van Woerden; Catharina Ziekenhuis:
Carien Miedema; Prinses Máxima Centrum voor Kinderoncologie: Wim Tissing; Slingeland
Ziekenhuis: Monique Jacobs, Elisabeth-TweeStedenziekenhuis: Charlie Obihara; Gelre Ziekenhuizen:
Annemarie Oudshoorn; St Jansdal Ziekenhuis: Annette Vernooij; Canisius-Wilhelmina Ziekenhuis:
Ingeborg Barts; Dijklander Ziekenhuis: Yolande Thomasse; Ommelander Ziekenhuis Groningen:
Bettina Auffarth; ZorgSaam Ziekenhuis: Joyce Goris; BovenIJ Ziekenhuis: Venje Boonstra; Curacao
Medical Center: Lindy Janssen, Shirley Lo-A-Njoe; Deventer Ziekenhuis: Jenneke Homan-van der
Veen; Elkerliek Ziekenhuis: Marianne Faber, Mijke Breukels; Zaans Medisch Centrum: Maarten
Rijpert, Leontien van der Aa; Tergooiziekenhuizen: Karin Miedema

Turkey: Betul Sozeri - University of health sciences, Istanbul; Gülçin Otar Yener - Şanlıurfa Research
and Education hospital; Yasemin Ozsurekci - Hacettepe University Ihsan Dogramaci Children's Hospital,
Ankara; Aslinur Ozkaya-Parlakay - Ankara City Hospital; Benhur Cetin - Erciyes University, Kayseri,
Turkey

United Kingdom: Ashish Chikermane - Birmingham Children's Hospital; Julia Kenny - Evelina London
Children's Hospital; Stefania Vergnano - Bristol Royal Hospital for Children; Simon Drysdale - St
George's University of London, London, UK; Karyn Moshal - Great Ormond Street Hospital for Children
NHS Foundation Trust, London

Uruguay: Federica Badia De Ferrari - Facultad Medicina Universidad Republica, Montevideo

United States of America: Duraisamy Balaguru - MassGeneral Hospital for Children, Boston, MA;
Matthew Oster - Children's Healthcare of Atlanta, Atlanta, GA, Emory University School of Medicine,
Atlanta, GA; Ashraf Harahsheh and Claire O’Connell Boogaard - Children’s National Hospital; George
Washington University School of Medicine & Health Sciences; NW Washington; Jocelyn Ang - Children's
Hospital of Michigan, Detroit, Michigan, Department of Pediatrics, Central Michigan University College
of Medicine, Mt. Pleasant, Michigan; Yonca Bulut - UCLA, Los Angeles, California; Tyler Harris - UPMC
Children's Hospital of Pittsburgh; Kirsten Dummer - Rady Children's Hospital, UC San Diego; Moshe
Arditi - Cedars Sinai Medical Center, Los Angeles

You might also like