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T cell numbers relate to bone involvement in Gaucher disease

dc.contributor.authorLACERDA, L.
dc.contributor.authorAROSA, F.A.
dc.contributor.authorLACERDA, R.
dc.contributor.authorCABEDA, J.
dc.contributor.authorPORTO, G.
dc.contributor.authorAMARAL, O.
dc.contributor.authorFortuna, A.
dc.contributor.authorPINTO, R.
dc.contributor.authorOLIVEIRA, P.
dc.contributor.authorMCLAREN, C.E.
dc.contributor.authorSA MIRANDA, C.
dc.contributor.authorDE SOUSA, M.
dc.date.accessioned2011-03-02T12:31:57Z
dc.date.available2011-03-02T12:31:57Z
dc.date.issued1999-04
dc.description.abstractBlood Cells Mol Dis. 1999 Apr;25(2):130-8. T cell numbers relate to bone involvement in Gaucher disease. Lacerda L, Arosa FA, Lacerda R, Cabeda J, Porto G, Amaral O, Fortuna A, Pinto R, Oliveira P, McLaren CE, Sá Miranda C, de Sousa M. Department of Genetics Neurobiology, Porto University, Portugal. Abstract The major elements of bone pathology in Gaucher disease are a failure of osteoclast and osteoblast function, resulting in osteopenia and also osteonecrosis. T lymphocytes have recently been found to be involved in the regulation of osteoblast/osteoclast activity in vitro. In the present report the peripheral blood T major lymphocyte subsets were investigated in a group of genotyped type 1 Gaucher disease patients. A total of 31 patients were studied: 21 non-splenectomized (5 N370S homozygotes) and 10 splenectomized (of whom 1 was a N370S homozygote). The results show that non-splenectomized patients present a decrease in absolute numbers of peripheral blood T lymphocytes, specially the CD4+ T subset. However, when patients were analyzed with respect to the presence of bone disease, the number of CD8+ T lymphocytes was found to be statistically significantly lower in patients presenting bone involvement. Furthermore, lower numbers of CD8+ T lymphocytes were significantly correlated with higher levels of plasma tartrate resistant acid phosphatase (TRAP) activity, a putative marker of osteoclast cell activity. These in vivo findings are in agreement with the results reached in vitro by others. They provide an additional marker of disease severity in Gaucher disease. In the group of genotyped Gaucher disease patients, the majority of the N370S homozygous patients presented a clinically milder phenotype, including the absence of bone involvement, confirming earlier reports predicting that a number of these patients may remain undiagnosed. Collectively the homozygosity for the N370S mutation and normal T cell numbers may provide additional markers for the clinical heterogeneity of Gaucher disease. PMID: 10389595 [PubMed - indexed for MEDLINEpor
dc.identifier.issn1079-9796
dc.identifier.urihttp://hdl.handle.net/10400.16/545
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherUnknownpor
dc.relation.publisherversionhttp://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WBV-45WHRR9-7&_user=5838510&_coverDate=04%2F30%2F1999&_rdoc=1&_fmt=high&_orig=gateway&_origin=gateway&_sort=d&_docanchor=&view=c&_acct=C000066143&_version=1&_urlVersion=0&_userid=5838510&md5=0efcfd5a037862478663443c75b0b343&searchtype=apor
dc.titleT cell numbers relate to bone involvement in Gaucher diseasepor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.titleBlood cells, molecules & diseasespor
person.familyNameFortuna
person.givenNameAna
person.identifier.orcid0000-0002-1296-5366
person.identifier.scopus-author-id35974338400
rcaap.rightsopenAccesspor
rcaap.typearticlepor
relation.isAuthorOfPublicationb65d1d1e-7f2c-4f84-8189-2c37e7a2632f
relation.isAuthorOfPublication.latestForDiscoveryb65d1d1e-7f2c-4f84-8189-2c37e7a2632f

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