BCG Moreau Vaccine Safety Profile and NK Cells-Double Protection Against Disseminated BCG Infection in Retrospective Study of BCG Vaccination in 52 Polish Children with Severe Combined Immunodeficiency.


Journal

Journal of clinical immunology
ISSN: 1573-2592
Titre abrégé: J Clin Immunol
Pays: Netherlands
ID NLM: 8102137

Informations de publication

Date de publication:
01 2020
Historique:
received: 22 02 2019
accepted: 14 10 2019
pubmed: 22 11 2019
medline: 12 2 2021
entrez: 22 11 2019
Statut: ppublish

Résumé

The aim of the study was to estimate the rate of adverse reactions to live BCG Moreau vaccine, manufactured by Biomed in Poland, in severe combined immunodeficiency (SCID) patients. The profiles of 52 SCID patients vaccinated at birth with BCG, hospitalized in Children's Memorial Health Institute, Warsaw (CMHI), in the years 1980-2015 were compared with those of 349 BCG-vaccinated SCID patients from other countries analyzed by Beatriz E. Marciano et al. in a retrospective study (Marciano et al. J Allergy Clin Immunol. 2014;133(4):1134-1141). Significantly less disseminated BCG infections (10 out of 52 SCID, 19%) occurred in comparison with Marciano study-119 out of 349, 34% (p = 0.0028), with no death in patients treated with SCID anti-TB drug, except one in lethal condition. In our study, disseminated BCG infection was observed only in SCID with T-B+NK- phenotype and significantly lower NK cell counts (p = 0.0161). NK cells do not influence on the frequency of local BCG reaction. A significantly higher number of hematopoietic stem cells transplantations (HSCT) were performed in CMHI study (p = 0.0001). Anti-TB treatment with at least two medicines was provided. The BCG Moreau vaccine produced in Poland, with well-documented genetic characteristics, seems to be safer than other BCG substrains used in other regions of the world. Importantly, NK cells seem to play a role in protecting SCID patients against disseminated BCG complications, which NK- SCID patients are more prone to. HSCT and TB therapy could be relevant due to the patients' survival and the fact that they protect against BCG infection.

Identifiants

pubmed: 31749033
doi: 10.1007/s10875-019-00709-1
pii: 10.1007/s10875-019-00709-1
pmc: PMC7082382
doi:

Substances chimiques

BCG Vaccine 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

138-146

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Auteurs

Ewa Bernatowska (E)

Department of Immunology, The Children's Memorial Health Institute, Warsaw, Poland. ewa.bernatowska@gmail.com.

Małgorzta Skomska-Pawliszak (M)

Department of Immunology, The Children's Memorial Health Institute, Warsaw, Poland.

Beata Wolska-Kuśnierz (B)

Department of Immunology, The Children's Memorial Health Institute, Warsaw, Poland.

Małgorzata Pac (M)

Department of Immunology, The Children's Memorial Health Institute, Warsaw, Poland.

Edyta Heropolitanska-Pliszka (E)

Department of Immunology, The Children's Memorial Health Institute, Warsaw, Poland.

Barbara Pietrucha (B)

Department of Immunology, The Children's Memorial Health Institute, Warsaw, Poland.

Katarzyna Bernat-Sitarz (K)

Department of Immunology, The Children's Memorial Health Institute, Warsaw, Poland.

Nel Dąbrowska-Leonik (N)

Department of Immunology, The Children's Memorial Health Institute, Warsaw, Poland.

Nadia Bohynikova (N)

Department of Immunology, The Children's Memorial Health Institute, Warsaw, Poland.

Barbara Piątosa (B)

Histocompatibility Laboratory, Children's Memorial Health Institute, Warsaw, Poland.

Anna Lutyńska (A)

Department of Medical Biology, The Cardinal Stefan Wyszyński Institute of Cardiology, Warsaw, Poland.

Ewa Augustynowicz (E)

Department of Epidemiology, National Institute of Public Health - National Institute of Hygiene, Warsaw, Poland.

Ewa Augustynowicz-Kopeć (E)

Department of Microbiology, National Tuberculosis Reference Laboratory, National Tuberculosis and Lung Diseases Research Institute, Warsaw, Poland.

Maria Korzeniewska-Koseła (M)

Department of Tuberculosis Epidemiology and Surveillance, National Tuberculosis and Lung Diseases Research Institute, Warsaw, Poland.

Maria Krasińska (M)

Department of Tuberculosis and Lung Disease, Mazovian Centre for Tuberculosis and Lung Disease, Otwock, Poland.

Katarzyna Krzysztopa-Grzybowska (K)

Department of Sera and Vaccines Evaluation, National Institute of Public Health - National Institute of Hygiene, Warsaw, Poland.

Anna Wieteska-Klimczak (A)

Department of Paediatrics, Nutrition and Metabolic Diseases, Children's Memorial Health Institute, Warsaw, Poland.

Janusz Książyk (J)

Department of Paediatrics, Nutrition and Metabolic Diseases, Children's Memorial Health Institute, Warsaw, Poland.

Teresa Jackowska (T)

Department of Paediatrics, Medical Centre of Postgraduate Education, Warsaw, Poland.
Department of Paediatrics, Bielanski Hospital, Warsaw, Poland.

Mirjam van den Burg (M)

Department of Immunohematology and Blood Transfusion (IHB), Leiden University Medical Center (LUMC), 2333, Leiden, ZA, Netherlands.

Jacques J M van Dongen (JJM)

Department of Immunohematology and Blood Transfusion (IHB), Leiden University Medical Center (LUMC), 2333, Leiden, ZA, Netherlands.

Jean-Laurent Casanova (JL)

St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, USA.
Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR 1163, Necker Hospital for Sick Children, Paris, France.
Paediatric Hematology-Immunology Unit, Necker Hospital for Sick Children, Paris, France.
Howard Hughes Medical Institute, New York, NY, USA.
Paris Descartes University, Imagine Institute, Paris, France.

Capucine Picard (C)

Paris Descartes University, Imagine Institute, Paris, France.
Study Centre for Primary Immunodeficiency, Necker-Enfants Malades Hospital, Assistance Publique des Hôpitaux de Paris (AP-HP), Paris, France.

Bożena Mikołuć (B)

Department of Paediatrics, Rheumatology, Immunology and Metabolic Bone Diseases, Medical University of Bialystok, Białystok, Poland.

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