The vaccine coverage and vaccine immunity status and risk factors of non-protective levels of antibodies against vaccines in children with juvenile idiopathic arthritis: cross-sectional Russian tertiary Centre study.
diphtheria
hepatitis B
juvenile idiopathic arthritis
measles
mumps
protective level of antibodies against vaccines
rubella
vaccines
Journal
Pediatric rheumatology online journal
ISSN: 1546-0096
Titre abrégé: Pediatr Rheumatol Online J
Pays: England
ID NLM: 101248897
Informations de publication
Date de publication:
05 Jul 2021
05 Jul 2021
Historique:
received:
12
01
2021
accepted:
10
04
2021
entrez:
6
7
2021
pubmed:
7
7
2021
medline:
4
1
2022
Statut:
epublish
Résumé
Immunosuppressive drugs, incomplete vaccine coverage, immune system dysregulation might be factors of a low level of anti-vaccine antibodies in JIA patients. The study aimed to evaluate vaccine coverage, post-vaccine immunity, and risk factors of non-protective levels of antibodies against measles, mumps, rubella, hepatitis B, and diphtheria in JIA patients. A cross-sectional study included 170 children diagnosed with JIA aged 2 to 17 years who received routine vaccinations against measles, rubella, mumps (MMR), diphtheria, and hepatitis B national vaccine schedule. In all patients, the levels of post-vaccination antibodies (IgG) for measles, rubella, mumps, hepatitis B, and diphtheria were measured with ELISA. Protective level of antibodies were 50% against hepatitis B, 52% - diphtheria, 58% - measles, 80% - mumps, 98% rubella. MMR's best coverage had patients with enthesitis-related arthritis-85%, compared to oligoarthritis-70%, polyarthritis-69%, systemic arthritis-63%. Diphtheria coverage was 50, 51, 46, 63%, respectively. Incomplete MMR vaccination had 39% patients, treated with biologics, 22% with methotrexate and 14% with NSAID (p = 0.025), and 61, 46, 36% for diphtheria (p = 0.021). Incomplete vaccination was a risk factor of non-protective level of antibodies against measles (HR = 2.03 [95%CI: 1.02; 4.0], p = 0.042), mumps (HR = 6.25 [95%CI: 2.13; 17.9], p = 0.0008) and diphtheria (HR = 2.39 [95%CI: 1.18; 4.85], p = 0.016) vaccines, as well as JIA category, biologics, corticosteroids and long-term methotrexate treatment for distinct vaccines. One-third part of JIA patients continued vaccination against MMR and diphtheria without serious adverse events and JIA flare. There were no differences between patients who continued MMR vaccination or denied in the means of JIA category and treatment options. Patients, continued diphtheria vaccination rare received methotrexate (p = 0.02), biologics (p = 0.004), but had higher levels of anti-diphtheria antibodies (p = 0.024) compare who omitted vaccination. Methotrexate (OR = 9.5 [95%CI: 1.004; 90.3]) and biologics (OR = 4.4 [95%CI: 1.6; 12.1]) were predictors of omitted diphtheria revaccination. Children with JIA may have lower anti-vaccine antibody levels and required routine checks, especially in children with incomplete vaccination, biologics, systemic arthritis, and long-term methotrexate treatment. Revaccination of JIA patients was safe and effective.
Sections du résumé
BACKGROUND
BACKGROUND
Immunosuppressive drugs, incomplete vaccine coverage, immune system dysregulation might be factors of a low level of anti-vaccine antibodies in JIA patients. The study aimed to evaluate vaccine coverage, post-vaccine immunity, and risk factors of non-protective levels of antibodies against measles, mumps, rubella, hepatitis B, and diphtheria in JIA patients.
METHODS
METHODS
A cross-sectional study included 170 children diagnosed with JIA aged 2 to 17 years who received routine vaccinations against measles, rubella, mumps (MMR), diphtheria, and hepatitis B national vaccine schedule. In all patients, the levels of post-vaccination antibodies (IgG) for measles, rubella, mumps, hepatitis B, and diphtheria were measured with ELISA.
RESULTS
RESULTS
Protective level of antibodies were 50% against hepatitis B, 52% - diphtheria, 58% - measles, 80% - mumps, 98% rubella. MMR's best coverage had patients with enthesitis-related arthritis-85%, compared to oligoarthritis-70%, polyarthritis-69%, systemic arthritis-63%. Diphtheria coverage was 50, 51, 46, 63%, respectively. Incomplete MMR vaccination had 39% patients, treated with biologics, 22% with methotrexate and 14% with NSAID (p = 0.025), and 61, 46, 36% for diphtheria (p = 0.021). Incomplete vaccination was a risk factor of non-protective level of antibodies against measles (HR = 2.03 [95%CI: 1.02; 4.0], p = 0.042), mumps (HR = 6.25 [95%CI: 2.13; 17.9], p = 0.0008) and diphtheria (HR = 2.39 [95%CI: 1.18; 4.85], p = 0.016) vaccines, as well as JIA category, biologics, corticosteroids and long-term methotrexate treatment for distinct vaccines. One-third part of JIA patients continued vaccination against MMR and diphtheria without serious adverse events and JIA flare. There were no differences between patients who continued MMR vaccination or denied in the means of JIA category and treatment options. Patients, continued diphtheria vaccination rare received methotrexate (p = 0.02), biologics (p = 0.004), but had higher levels of anti-diphtheria antibodies (p = 0.024) compare who omitted vaccination. Methotrexate (OR = 9.5 [95%CI: 1.004; 90.3]) and biologics (OR = 4.4 [95%CI: 1.6; 12.1]) were predictors of omitted diphtheria revaccination.
CONCLUSION
CONCLUSIONS
Children with JIA may have lower anti-vaccine antibody levels and required routine checks, especially in children with incomplete vaccination, biologics, systemic arthritis, and long-term methotrexate treatment. Revaccination of JIA patients was safe and effective.
Identifiants
pubmed: 34225748
doi: 10.1186/s12969-021-00594-2
pii: 10.1186/s12969-021-00594-2
pmc: PMC8256221
doi:
Substances chimiques
Antibodies
0
Vaccines
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
108Subventions
Organisme : Ministry of Science and Higher Education of the Russian Federation
ID : 075-15-2020-901
Références
Ann Rheum Dis. 2020 Jan;79(1):39-52
pubmed: 31413005
Z Rheumatol. 2007 Mar;66(2):111-2, 114-8, 120
pubmed: 17364157
Ann Rheum Dis. 2014 Apr;73(4):728-34
pubmed: 23505231
Clin Exp Rheumatol. 2020 Jan-Feb;38(1):164-170
pubmed: 31577215
Rheumatology (Oxford). 2012 Nov;51(11):2046-50
pubmed: 22864995
Reumatologia. 2015;53(2):56-60
pubmed: 27407228
RMD Open. 2019 Sep 9;5(2):e001035
pubmed: 31565247
EMBO Mol Med. 2018 May;10(5):
pubmed: 29685959
Clin Exp Rheumatol. 2008 Jan-Feb;26(1 Suppl 48):S67-73
pubmed: 18570757
J Clin Med. 2020 Nov 20;9(11):
pubmed: 33233818
J Rheumatol. 2013 Sep;40(9):1626-7
pubmed: 23997002
J Rheumatol. 2004 Feb;31(2):390-2
pubmed: 14760812
JAMA. 2013 Jun 19;309(23):2449-56
pubmed: 23780457
Vaccine. 2020 Oct 14;38(44):6914-6921
pubmed: 32888740
Rheum Dis Clin North Am. 2017 Feb;43(1):1-13
pubmed: 27890167
Pediatr Rheumatol Online J. 2020 Feb 22;18(1):19
pubmed: 32087715
Genet Mol Biol. 2021 Jan 29;44(1 Suppl 1):e20200256
pubmed: 33533395
Mod Rheumatol. 2016;26(3):368-71
pubmed: 26471922
Ann Rheum Dis. 2004 Sep;63(9):1128-30
pubmed: 15308522
N Engl J Med. 1994 Nov 24;331(21):1397-402
pubmed: 7969278
Clin Exp Rheumatol. 2013 Nov-Dec;31(6):969-73
pubmed: 23806191
Mod Rheumatol. 2015 May;25(3):335-43
pubmed: 25381726
Int J Rheumatol. 2020 Aug 4;2020:1078914
pubmed: 32831849
Lancet. 1988 Oct 15;2(8616):909
pubmed: 2902357
Arthritis Res Ther. 2019 Oct 28;21(1):218
pubmed: 31661011
Clin Rheumatol. 2010 Jun;29(6):605-13
pubmed: 20140692
RMD Open. 2019 Sep 19;5(2):e001041
pubmed: 31673420
Eur J Pediatr. 2011 Feb;170(2):157-67
pubmed: 20556424
Ann Rheum Dis. 2011 Oct;70(10):1704-12
pubmed: 21813547
Lancet Rheumatol. 2021 Apr;3(4):e243-e245
pubmed: 33655219
Arthritis Res Ther. 2020 Oct 29;22(1):258
pubmed: 33121528
Vaccine. 2020 Feb 24;38(9):2198-2201
pubmed: 31987692
Curr Rheumatol Rep. 2020 May 20;22(7):26
pubmed: 32436130
Ann Rheum Dis. 2012 Jun;71(6):948-54
pubmed: 22172491