The differential diagnosis of inflammatory joint disease in maternal-fetal microchimerism

Reda, Seme Youssef; Martins, Marina Lobato

doi:10.1590/s1676-24442013000600004

Cited by 2 publications

(8 citation statements)

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“…The differential diagnosis of inflammatory joint disease in maternal-fetal microchimerism Reda & Martins. 2013 Case report…”

Section: Resultsmentioning

confidence: 99%

“…In relation to language, 83.3% (n = 5) are in English (Wu et al, 2018;Aloisio et al, 2017;Clemente et al,2017;Thompson et al, 2017;Reda;Martins, 2013) and 16.6% (n = 1) in French (Dubois et al, 2017). The type of study 83.3% (n = 5) are observational studies and 16.6% (n = 1) refer to case reports.…”

Section: Resultsmentioning

confidence: 99%

“…According to the literature review, human chimerism is the presence of more than one population of genetically differentiated cells in an individual (Yu et al, 2011). Articles that met all the inclusion and exclusion criteria are presented in greater number in the English language (Aloisio et al, 2017;Clemente et al, 2017;Reda & Martins, 2013;Thompson et al, 2017;Wu et al, 2018), since the best journals and the best impact factors are in that language, so the preference for publications in that language prevails. In addition, English is considered a universal and widely accessible language.…”

Section: Discussionmentioning

confidence: 99%

“…The article by Reda and Martins (2013) reports the case of a 49-year-old female patient with three gestations, all of them male, whose last pregnancy occurred 20 years ago. The patient was a regular donor at the Guarapuava Regional Blood…”

Section: Discussionmentioning

confidence: 99%

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Laboratory diagnosis for human chimerism: systematic review

Weber

Rocha

Nogueira

et al. 2022

RSD

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The objective of the article was to perform a systematic review of the literature on laboratory diagnosis for human chimerism. The Medical Literature Analysis and Retrieval System Online (Medline), Public Medline or Publisher Medline (PubMed), Scientific Electronic Library (Scielo), Latin American and Caribbean Literature on Health Sciences (LILACS) databases were searched according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) methodology. Articles were included that had as an endpoint evidencing the diagnosis for chimerism in humans, published in the period from 2005 to 2018. Articles whose endpoint was the occurrence of other types of chimerism were excluded. To compose the study, 36 articles were pre-selected, of these only 6 met the inclusion criteria given by the PRISMA method. Regarding the diagnostics used in the articles to detect chimerism, in 100% of the articles there is reference to the Polymerase Chain Reaction (PCR) combined with other techniques as the main diagnostic for detection of chimerism, such as Fluorescent in situ hybridization (FISH), Short Tandem Repeats (STR), Single Nucleotide Polymorphisms (SNPs), Small Insertions and Deletions (INDELs), Single Molecular Inversion Molecular Probes (smMIP) and TaqMan type molecular probes. These combined techniques have many advantages and are decisive for the scientific community in revealing this genetic condition. Thus, it is concluded that there are few techniques that allow a specific diagnosis for chimerism, however, the existing techniques are effective in identifying this genetic condition.

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“…The differential diagnosis of inflammatory joint disease in maternal-fetal microchimerism Reda & Martins. 2013 Case report…”

Section: Resultsmentioning

confidence: 99%

Section: Resultsmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

See 2 more Smart Citations

Laboratory diagnosis for human chimerism: systematic review

Weber

Rocha

Nogueira

et al. 2022

RSD

View full text Add to dashboard Cite

show abstract

“…An overview of the results and data obtained from related studies over recent 10-15 years demonstrates different roles for fetal microchimeric cell in the maternal body, including natural microchimerism (no biological role), utility (damaged tissue repair) and pathogenesis (causing autoimmune disease and cancer) (91)(92)(93)(94)(95)(96)(97).…”

Section: Resultsmentioning

confidence: 99%

A Survey on the Role of Fetal Microchimerism in the Maternal Body

Bozorg-Ghalati

2015

Journal of Advanced Medical Sciences and Applied Technologies

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History of fetal microchimerism finding For the first time, in the early 1970s fetal microchimerism was identified in the mother's peripheral blood and lymphocytes cultured as a natural event in pregnant women (5-7). The pathogenicity theory of these cells was first proposed by Nelson in 1996. He noted that transfer of the fetal cells to the maternal body following pregnancy may lead to maternal immune response to these foreign cells and brings about some reactions like graft-versus-host disease and autoimmune reaction (8). Based on the ability of these cells to differentiate into multiple cell lineages or very early stem cells progenitor, they have been

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The differential diagnosis of inflammatory joint disease in maternal-fetal microchimerism

Cited by 2 publications

References 3 publications

Laboratory diagnosis for human chimerism: systematic review

Laboratory diagnosis for human chimerism: systematic review

A Survey on the Role of Fetal Microchimerism in the Maternal Body

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