Predictive value of immunological markers in systemic sclerosis

被引:8
|
作者
Bobeica, Carmen [1 ]
Niculet, Elena [1 ]
Halip, Alina [2 ]
Gheuca-Solovastru, Laura [3 ]
Draganescu, Miruna [4 ]
Popescu, Ioana [2 ]
Onisor, Cristian [1 ]
Chirobocea, Silvia [5 ]
Lungu, Mihaela [4 ]
Craescu, Mihaela [1 ]
机构
[1] Dunarea de Jos Univ Galati, Fac Med & Pharm, Dept Morphol & Funct Sci, 35 Alexandru Ioan Cuza St, Galati 800216, Romania
[2] Gr T Popa Univ Med & Pharm, Doctoral Sch, Dept Dermatovenereol, 16 Univ St, Iasi 700115, Romania
[3] Gr T Popa Univ Med & Pharm, Dept Clin Dermatovenereol, Fac Med & Pharm, Iasi 700115, Romania
[4] Dunarea de Jos Univ Galati, Fac Med & Pharm, Clin Med Dept, Galati 800216, Romania
[5] Municipal Emergency Hosp, Dept Neurol, Moinesti 605400, Romania
关键词
systemic sclerosis; antinuclear antibodies; immunological profile; anti-Scl70; anticentromere; paraneoplastic; ADVERSE-REACTIONS; CLASSIFICATION; SCLERODERMA; FEATURES;
D O I
10.3892/etm.2021.10426
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Systemic sclerosis (SSc) is a collagenosis characterized by excessive deposition of collagen in the skin and viscera, in a background of immune disorder. The immunological profile of SSc often shows elevated levels of antinuclear antibodies (ANAs). However, many authors have identified cases of SSc having normal ANA levels, framed as paraneoplastic SSc. Among patients with negative ANAs in our group, we did not identify any neoplastic process that could support this hypothesis. The extended detection of autoantibodies is extremely useful in establishing the subset of SSc. Thus, anti-Scl70 antibodies are specific for the diffuse subset of SSc, while anticentromere antibodies (ACAs) have specificity for a limited subset. However, studies have shown the existence of cases of diffuse SSc having high titers of ACAs and cases of limited SSc with high titers of anti-Scl70 antibodies. This indicates an inconsistent association between the disease subset and the autoantibodies specific to each subset. Our study found a more balanced consistency between disease subsets and autoantibodies specific for each subset. Therefore, the percentages of patients having an immunological profile inconsistent with the subset of SSc, are lower than those found by other authors. This observation opens the perspective of larger studies on the immunological profile in SSc.
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页数:5
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