Tolerance and humoral immune response to the yellow fever vaccine in sickle cell disease children treated with hydroxyurea: a multicentre prospective study.


Journal

Journal of travel medicine
ISSN: 1708-8305
Titre abrégé: J Travel Med
Pays: England
ID NLM: 9434456

Informations de publication

Date de publication:
14 04 2021
Historique:
received: 22 10 2020
revised: 11 01 2021
pubmed: 8 2 2021
medline: 16 6 2021
entrez: 7 2 2021
Statut: ppublish

Résumé

Sickle cell disease (SCD) children are frequent travellers to countries where yellow fever (YF) is endemic, but there are no data regarding the safety and immunogenicity of the vaccine in such children treated with hydroxyurea (HU). The main objective of this study was to compare the tolerance and immune response to YF vaccination in SCD children treated or not with HU. SCD children < 18 years attending the international travel clinics of three large paediatric centres and requiring a first YF vaccination were included in a prospective study. Adverse events were collected 2 weeks after vaccination. YF vaccine antibody titres were measured ~6 months after vaccination. Among the 52 SCD children vaccinated against YF, 17 (33%) were treated with HU. Only mild adverse events, mainly fever and local reaction, were observed in the HU group with a similar frequency in the non-HU group (57 and 35%, respectively, P = 0.30). YF antibody titres were measured in 15/17 patients in the HU group and 23/35 patients in the non-HU group after a median of 6.0 months (3.5-8.5) following vaccination. The geometric mean of YF antibody titre was similar in both groups. A protective antibody level was observed in 85% of the children in the HU group vs 100% in the non-HU group (P = 0.14), suggesting a lower effectiveness of the vaccine in patients on HU similarly to what has been described in patients on immune suppressive therapy for other vaccines. YF vaccination seems to be safe and efficient in SCD children treated with HU. Considering the potential risk of severe complications in cases of YF while travelling in Africa for those patients, the benefit-to-risk ratio argues for YF vaccination in all SCD children. Control of a protective antibody titre may also be useful to ascertain an adequate response in those treated with HU.

Sections du résumé

BACKGROUND
Sickle cell disease (SCD) children are frequent travellers to countries where yellow fever (YF) is endemic, but there are no data regarding the safety and immunogenicity of the vaccine in such children treated with hydroxyurea (HU). The main objective of this study was to compare the tolerance and immune response to YF vaccination in SCD children treated or not with HU.
METHOD
SCD children < 18 years attending the international travel clinics of three large paediatric centres and requiring a first YF vaccination were included in a prospective study. Adverse events were collected 2 weeks after vaccination. YF vaccine antibody titres were measured ~6 months after vaccination.
RESULTS
Among the 52 SCD children vaccinated against YF, 17 (33%) were treated with HU. Only mild adverse events, mainly fever and local reaction, were observed in the HU group with a similar frequency in the non-HU group (57 and 35%, respectively, P = 0.30). YF antibody titres were measured in 15/17 patients in the HU group and 23/35 patients in the non-HU group after a median of 6.0 months (3.5-8.5) following vaccination. The geometric mean of YF antibody titre was similar in both groups. A protective antibody level was observed in 85% of the children in the HU group vs 100% in the non-HU group (P = 0.14), suggesting a lower effectiveness of the vaccine in patients on HU similarly to what has been described in patients on immune suppressive therapy for other vaccines.
CONCLUSION
YF vaccination seems to be safe and efficient in SCD children treated with HU. Considering the potential risk of severe complications in cases of YF while travelling in Africa for those patients, the benefit-to-risk ratio argues for YF vaccination in all SCD children. Control of a protective antibody titre may also be useful to ascertain an adequate response in those treated with HU.

Identifiants

pubmed: 33550421
pii: 6129658
doi: 10.1093/jtm/taab013
pii:
doi:

Substances chimiques

Yellow Fever Vaccine 0
Hydroxyurea X6Q56QN5QC

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© International Society of Travel Medicine 2021. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Berengere Koehl (B)

Department of Haematology, Reference Centre of Sickle Cell Disease, Hôpital Robert Debré, APHP, 48 Bd Sérurier, Paris 75019, France.
Université de Paris, 48 Bld Serurier, 75019, Paris, France.
INSERM UMRS 1134, BIGR, 6 rue Alexandre Cabanel, 75015, Paris, France.

Camille Aupiais (C)

INSERM UMRS 1123, ECEVE, 10 avenue de Verdun 75010, Paris, France.
Department of Paediatrics Emergency, Jean Verdier Hospital, APHP, Bondy, France.

Nelly Schinckel (N)

Department of General Paediatrics and Infectious Diseases, Robert Debré Hospital, APHP, Paris, France.

Pierre Mornand (P)

Department of General Paediatrics, Centre for Sickle Cell Disease, Trousseau Hospital, APHP, Sorbonne Université, Paris, France.

Marie-Hélène Odièvre (MH)

INSERM UMRS 1134, BIGR, 6 rue Alexandre Cabanel, 75015, Paris, France.
Department of General Paediatrics, Centre for Sickle Cell Disease, Trousseau Hospital, APHP, Sorbonne Université, Paris, France.

Assa Niakate (A)

Department of General Paediatrics, Centre for Sickle Cell Disease, Trousseau Hospital, APHP, Sorbonne Université, Paris, France.

Valentine Brousse (V)

INSERM UMRS 1134, BIGR, 6 rue Alexandre Cabanel, 75015, Paris, France.
Department of General Paediatrics, Necker-Enfants malades hospital, APHP, 149 rue de Sevres, 75015, Paris, France.

Ghislaine Ithier (G)

Department of Haematology, Reference Centre of Sickle Cell Disease, Hôpital Robert Debré, APHP, 48 Bd Sérurier, Paris 75019, France.

Florence Missud (F)

Department of Haematology, Reference Centre of Sickle Cell Disease, Hôpital Robert Debré, APHP, 48 Bd Sérurier, Paris 75019, France.

Laurent Holvoet (L)

Department of Haematology, Reference Centre of Sickle Cell Disease, Hôpital Robert Debré, APHP, 48 Bd Sérurier, Paris 75019, France.

Malika Benkerrou (M)

Department of Haematology, Reference Centre of Sickle Cell Disease, Hôpital Robert Debré, APHP, 48 Bd Sérurier, Paris 75019, France.
INSERM UMRS 1123, ECEVE, 10 avenue de Verdun 75010, Paris, France.

Frederic Sorge (F)

Department of Haematology, Reference Centre of Sickle Cell Disease, Hôpital Robert Debré, APHP, 48 Bd Sérurier, Paris 75019, France.

Albert Faye (A)

Université de Paris, 48 Bld Serurier, 75019, Paris, France.
INSERM UMRS 1123, ECEVE, 10 avenue de Verdun 75010, Paris, France.
Department of General Paediatrics and Infectious Diseases, Robert Debré Hospital, APHP, Paris, France.

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