Effect of vitamin D replacement on immunological biomarkers in patients with multiple sclerosis

dc.contributor.authorMrad, May F.
dc.contributor.authorEl-Ayoubi, Nabil K.
dc.contributor.authorEsmerian, Maria O.
dc.contributor.authorKazan, Jalal M.
dc.contributor.authorKhoury, Samia J.
dc.contributor.departmentNeurology
dc.contributor.departmentPathology and Laboratory Medicine
dc.contributor.departmentSpecialized Clinical Programs and Services
dc.contributor.departmentNehme and Therese Tohme Multiple Sclerosis (MS) Center
dc.contributor.departmentAbu-Haidar Neuroscience Institute (AHNI)
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:07:30Z
dc.date.available2025-01-24T12:07:30Z
dc.date.issued2017
dc.description.abstractWe aimed to investigate the immunologic effects of vitamin D replacement in RRMS patients. In a controlled single center study, patients deficient in 25-hydroxyvitamin D (serum level < 25 ng/ml) received 10,000 IU/week cholecalciferol for 3 months. Sufficient vitamin D patients (serum level > 35 ng/ml) were followed for the same period. Assessments were performed at baseline and at 3 months. 25-hydroxyvitamin D levels increased significantly from baseline to month-3 in the deficient group after treatment and remained stable in the sufficient group. We observed a decreased interferon-γ (IFNγ) secretion by CD4+ T cells in vitamin D deficient group but not in the sufficient group, and a negative correlation between baseline serum vitamin D and IFNγ production. There was no change in the frequency of T helper or regulatory T cell subsets in either group. Increasing serum levels of 25-hydroxyvitamin D are associated with decreased production of IFNγ by CD4+ T cells. © 2017 Elsevier Inc.
dc.identifier.doihttps://doi.org/10.1016/j.clim.2017.05.017
dc.identifier.eid2-s2.0-85019894426
dc.identifier.pmid28536054
dc.identifier.urihttp://hdl.handle.net/10938/31541
dc.language.isoen
dc.publisherAcademic Press Inc.
dc.relation.ispartofClinical Immunology
dc.sourceScopus
dc.subjectCytometric bead array
dc.subjectImmunophenotyping
dc.subjectInterferon gamma
dc.subjectRelapsing remitting multiple sclerosis
dc.subjectT cells
dc.subjectVitamin d
dc.subjectAdult
dc.subjectCd4-positive t-lymphocytes
dc.subjectCholecalciferol
dc.subjectControlled before-after studies
dc.subjectCytokines
dc.subjectFemale
dc.subjectHumans
dc.subjectInterferon-gamma
dc.subjectMale
dc.subjectMiddle aged
dc.subjectMultiple sclerosis, relapsing-remitting
dc.subjectTreatment outcome
dc.subjectVitamin d deficiency
dc.subjectVitamins
dc.subjectYoung adult
dc.subject25 hydroxyvitamin d
dc.subjectBeta1a interferon
dc.subjectCd161 antigen
dc.subjectCd3 antibody
dc.subjectCd3 antigen
dc.subjectCd4 antibody
dc.subjectCd4 antigen
dc.subjectChemokine receptor ccr6
dc.subjectGamma interferon
dc.subjectGranulocyte macrophage colony stimulating factor
dc.subjectInterferon beta serine
dc.subjectInterleukin 10
dc.subjectInterleukin 17
dc.subjectInterleukin 2
dc.subjectInterleukin 23 receptor
dc.subjectInterleukin 4
dc.subjectInterleukin 6
dc.subjectTumor necrosis factor
dc.subject25-hydroxyvitamin d
dc.subjectColecalciferol
dc.subjectCytokine
dc.subjectVitamin
dc.subjectArticle
dc.subjectCd4+ t lymphocyte
dc.subjectClinical article
dc.subjectClinical assessment
dc.subjectControlled study
dc.subjectDrug effect
dc.subjectDrug megadose
dc.subjectHelper cell
dc.subjectHuman
dc.subjectIn vivo study
dc.subjectMultiple sclerosis
dc.subjectPriority journal
dc.subjectRegulatory t lymphocyte
dc.subjectTherapy effect
dc.subjectTreatment duration
dc.subjectVitamin blood level
dc.subjectVitamin supplementation
dc.subjectAnalogs and derivatives
dc.subjectBlood
dc.subjectComplication
dc.subjectEpidemiology
dc.subjectImmunology
dc.titleEffect of vitamin D replacement on immunological biomarkers in patients with multiple sclerosis
dc.typeArticle

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