TY - JOUR
T1 - A monocentric cohort of obstetric seronegative anti-phospholipid syndrome
AU - Truglia, Simona
AU - Capozzi, Antonella
AU - Mancuso, Silvia
AU - Recalchi, Serena
AU - Spinelli, Francesca Romana
AU - Perricone, Carlo
AU - De Carolis, Caterina
AU - Manganelli, Valeria
AU - Riitano, Gloria
AU - Garofalo, Tina
AU - Longo, Agostina
AU - De Carolis, Sara
AU - Alessandri, Cristiano
AU - Misasi, Roberta
AU - Valesini, Guido
AU - Sorice, Maurizio
AU - Conti, Fabrizio
PY - 2018
Y1 - 2018
N2 - The present study was conducted to diagnose obstetric anti-phospholipid syndrome (OAPS) in patients with clinical signs suggestive of anti-phospholipid syndrome (APS), but persistently negative for conventional anti-phospholipid antibodies (aPL). Sera from 61 obstetrical seronegative APS (SN-APS) patients were analyzed for anti-cardiolipin antibodies (aCL) using thin-layer chromatography (TLC)-immunostaining, for anti-cardiolipin/vimentin antibodies (aCL/Vim), anti-phosphatidylserine/prothrombin antibodies, IgA anti-β 2 glycoprotein I antibodies (aβ 2 GPI), and IgA aCL antibodies by enzyme-linked immunosorbent assay. Taken together, our findings show that in 50 out of 61 SN-APS (81.9%) at least one aPL/cofactor antibody was detected using the assays under test. Results revealed that 76% of SN-APS patients resulted positive for aCL by TLC-immunostaining, 54% for aCL/Vim, 12% for aPS/PT, 4% for IgA aβ 2 GPI, and 2% for IgA aCL. Thirty-five out of 61 patients were followed up and the tests were repeated on two occasions, at least 12 weeks apart. Twenty-six out of 35 SN-APS (74.3%) were positive at least one non-conventional test; only 2 patients (5.7%) did not confirm the positivity to the second test. These findings suggest that non-conventional tests, mainly aCL/Vim and aCL detected by TLC-immunostaining, seem to be the most sensitive approaches for finding out aPL in patients with obstetric SN-APS. The use of these tests can be useful for accurate and timely diagnosis of patients with obstetrical APS who are negative for conventional laboratory criteria markers.
AB - The present study was conducted to diagnose obstetric anti-phospholipid syndrome (OAPS) in patients with clinical signs suggestive of anti-phospholipid syndrome (APS), but persistently negative for conventional anti-phospholipid antibodies (aPL). Sera from 61 obstetrical seronegative APS (SN-APS) patients were analyzed for anti-cardiolipin antibodies (aCL) using thin-layer chromatography (TLC)-immunostaining, for anti-cardiolipin/vimentin antibodies (aCL/Vim), anti-phosphatidylserine/prothrombin antibodies, IgA anti-β 2 glycoprotein I antibodies (aβ 2 GPI), and IgA aCL antibodies by enzyme-linked immunosorbent assay. Taken together, our findings show that in 50 out of 61 SN-APS (81.9%) at least one aPL/cofactor antibody was detected using the assays under test. Results revealed that 76% of SN-APS patients resulted positive for aCL by TLC-immunostaining, 54% for aCL/Vim, 12% for aPS/PT, 4% for IgA aβ 2 GPI, and 2% for IgA aCL. Thirty-five out of 61 patients were followed up and the tests were repeated on two occasions, at least 12 weeks apart. Twenty-six out of 35 SN-APS (74.3%) were positive at least one non-conventional test; only 2 patients (5.7%) did not confirm the positivity to the second test. These findings suggest that non-conventional tests, mainly aCL/Vim and aCL detected by TLC-immunostaining, seem to be the most sensitive approaches for finding out aPL in patients with obstetric SN-APS. The use of these tests can be useful for accurate and timely diagnosis of patients with obstetrical APS who are negative for conventional laboratory criteria markers.
KW - Anti-phosphatidylserine/prothrombin
KW - Anti-phospholipid syndrome
KW - Anti-vimentin/cardiolipin
KW - Immunology
KW - Immunology and Allergy
KW - Seronegative anti-phospholipid syndrome
KW - Thin-layer chromatography
KW - Anti-phosphatidylserine/prothrombin
KW - Anti-phospholipid syndrome
KW - Anti-vimentin/cardiolipin
KW - Immunology
KW - Immunology and Allergy
KW - Seronegative anti-phospholipid syndrome
KW - Thin-layer chromatography
UR - http://hdl.handle.net/10807/132719
UR - https://www.frontiersin.org/articles/10.3389/fimmu.2018.01678/full
U2 - 10.3389/fimmu.2018.01678
DO - 10.3389/fimmu.2018.01678
M3 - Article
SN - 1664-3224
VL - 9
SP - 1678
EP - 1678
JO - Frontiers in Immunology
JF - Frontiers in Immunology
ER -