Prospective study of live attenuated vaccines for patients receiving immunosuppressive agents.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 27 03 2020
accepted: 21 09 2020
entrez: 1 10 2020
pubmed: 2 10 2020
medline: 15 12 2020
Statut: epublish

Résumé

Patients receiving immunosuppressive agents are at risk of life-threatening infections. However, live vaccines are generally contraindicated in them. We conducted a prospective study regarding live attenuated vaccines for them. Patients elder than one year of age with immunosuppressive agents who showed negative or borderline antibody titers (virus-specific IgG levels < 4.0) against one or more of measles, rubella, varicella, and mumps and fulfilled the criteria (CD4 cell counts ≥ 500/mm3, stimulation index of lymphocyte blast transformation by PHA ≥ 101.6, serum IgG level ≥ 300 mg/dl, no steroid use or prednisolone < 1 mg/kg/day or < 2 mg/kg/2 days, trough levels of tacrolimus or cyclosporine were < 10 ng/ml or < 100 ng/ml and under good control of primary disease) were enrolled. Sixty-four vaccinations were administered to 32 patients. The seroconversion rates for measles, rubella, varicella, and mumps were 80.0%, 100.0%, 59.1%, and 69.2%, respectively. No life-threatening adverse events were observed, although one patient suffered from vaccine-strain varicella who showed cellular and humoral immunodeficiency (CD4 cell counts = 511/mm3, stimulation index of lymphocyte blast transformation by PHA = 91.1, serum IgG level = 208 mg/dl). This girl was immunized before we established the criteria for vaccination. Immunization with live attenuated vaccines for patients receiving immunosuppressive agents might be effective and safe if their cellular and humoral immunological parameters are within normal levels. However, determining the criteria for vaccination by immunological parameters should be established to guarantee the safety of live vaccines in the future. Clinical Trial Registration: UMIN Clinical Trials Registry (UMIN-CTR) UMIN000007710. The date of registration: 2012/4/13.

Identifiants

pubmed: 33002085
doi: 10.1371/journal.pone.0240217
pii: PONE-D-20-06737
pmc: PMC7529194
doi:

Substances chimiques

Antibodies, Viral 0
Immunosuppressive Agents 0
Vaccines, Attenuated 0
Viral Vaccines 0

Banques de données

UMIN-CTR
['UMIN000007710']

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0240217

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Koichi Kamei (K)

Division of Nephrology and Rheumatology, National Center for Child Health and Development, Tokyo, Japan.

Isao Miyairi (I)

Division of Infectious Diseases, National Center for Child Health and Development, Tokyo, Japan.

Kenji Ishikura (K)

Division of Nephrology and Rheumatology, National Center for Child Health and Development, Tokyo, Japan.
Department of Pediatrics, Kitasato University School of Medicine, Kanagawa, Japan.

Masao Ogura (M)

Division of Nephrology and Rheumatology, National Center for Child Health and Development, Tokyo, Japan.

Kensuke Shoji (K)

Division of Infectious Diseases, National Center for Child Health and Development, Tokyo, Japan.

Katsuhiro Arai (K)

Division of Gastroenterology, National Center for Child Health and Development, Tokyo, Japan.

Reiko Ito (R)

Department of General Pediatrics, National Center for Child Health and Development, Tokyo, Japan.

Toshinao Kawai (T)

Division of Immunology, National Center for Child Health and Development, Tokyo, Japan.

Shuichi Ito (S)

Division of Nephrology and Rheumatology, National Center for Child Health and Development, Tokyo, Japan.
Department of Pediatrics, Yokohama City University, Kanagawa, Japan.

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Classifications MeSH