scholarly journals Variation in antinuclear antibody detection by automated indirect immunofluorescence analysis

2018 ◽  
Vol 78 (6) ◽  
pp. e48-e48 ◽  
Author(s):  
Lieve Van Hoovels ◽  
Sofie Schouwers ◽  
Stefanie Van den Bremt ◽  
Xavier Bossuyt
Author(s):  
Sofie Schouwers ◽  
Myriam Bonnet ◽  
Patrick Verschueren ◽  
René Westhovens ◽  
Daniel Blockmans ◽  
...  

2021 ◽  
Vol 10 (17) ◽  
pp. 3866
Author(s):  
Nada Tomić Sremec ◽  
Ana Kozmar ◽  
Josip Sremec ◽  
Branimir Anić ◽  
Drago Batinić

In this study, we aimed to assess the prevalence of uncommon staining patterns found during testing for the presence of antinuclear antibodies (ANA) and to determine their association with certain antibodies and clinical diagnoses. Presence of ANA and the staining pattern was determined in 10955 samples using indirect immunofluorescence (IIF) on HEp-2 cells. ANA-positive samples were assessed for presence of 14 specific antibody types using a microbead based system. Demographic data (age, sex) and clinical diagnoses were collected from the referral documentation. Particular staining patterns were then compared with a representative comparison group comprised of samples with common staining patterns using these criteria. There were 22 patterns present in less than 3% of samples each and these were jointly present in 42.43% of ANA-positive samples. Specific antibodies were found in proportions similar to the comparison group (46.06%) and varied significantly between patterns. Likewise, there were significant differences in antibody distribution in particular patterns. Some patterns were associated with presence of rheumatic diseases or inflammatory arthropathies, while in others there was a concurrent diagnosis of liver disease, or a neoplastic process. Many of the uncommon IIF patterns have distinctive characteristics that warrant further investigation in order to determine their role in diagnosing various diseases, not limited only to the illnesses of the rheumatic spectrum. IIF on HEp-2 cells remains an irreplaceable method because of the diversity of ANA, only a number of which can be detected using other standardised methods.


2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Shiyi Zheng ◽  
Yukang Huang ◽  
Hongyun Huang ◽  
Bin Yu ◽  
Ni Zhou ◽  
...  

Abstract Background Nosema bombycis is a unicellular eukaryotic pathogen of the silkworm, Bombyx mori, and is an economic and occupational hazard in the silkworm industry. Because of its long incubation period and horizontal and vertical transmission, it is subject to quarantine measures in sericulture production. The microsporidian life-cycle includes a dormant extracellular phase and intracellular proliferation phase, with the proliferation period being the most active period. This latter period lacks spore wall protection and may be the most susceptible stage for control. Methods In order to find suitable target for the selective breeding of N. bombycis-resistant silkworm strains, we screen highly expressed membrane proteins from the transcriptome data of N. bombycis. The subcellular localization of the candidate protein was verified by Indirect immunofluorescence analysis (IFA) and immunoelectron microscopy (IEM), and its role in N. bombycis proliferation was verified by RNAi. Results The N. bombycis protein (NBO_76g0014) was identified as a transmembrane protein and named NbTMP1. It is homologous with hypothetical proteins NGRA_1734 from Nosema granulosis. NbTMP1 has a transmembrane region of 23 amino acids at the N-terminus. Indirect immunofluorescence analysis (IFA) results suggest that NbTMP1 is secreted on the plasma membrane as the spores develop. Western blot and qRT-PCR analysis showed that NbTMP1 was expressed in all developmental stages of N. bombycis in infected cells and in the silkworm midgut. Downregulation of NbTMP1 expression resulted in significant inhibition of N. bombycis proliferation. Conclusions We confirmed that NbTMP1 is a membrane protein of N. bombycis. Reduction of the transcription level of NbTMP1 significantly inhibited N. bombycis proliferation, and this protein may be a target for the selective breeding of N. bombycis-resistant silkworm strains.


2011 ◽  
Vol 30 (10) ◽  
pp. 1363-1368 ◽  
Author(s):  
Victoria K. Shanmugam ◽  
Donna R. Swistowski ◽  
Nicole Saddic ◽  
Hong Wang ◽  
Virginia D. Steen

2013 ◽  
Vol 72 (Suppl 3) ◽  
pp. A279.2-A279
Author(s):  
F. Zarabpouri ◽  
M.-L. V. Zambales ◽  
V. O. Miralles ◽  
T. T. Pizarro ◽  
J. M. Popov ◽  
...  

2004 ◽  
Vol 7 (1) ◽  
pp. 13-18
Author(s):  
V. Anuradha ◽  
Arvind Chopra ◽  
Allan S. Sturgess ◽  
John P. Edmonds

2013 ◽  
Vol 415 ◽  
pp. 101-106 ◽  
Author(s):  
Xavier Bossuyt ◽  
Sarah Cooreman ◽  
Heidi De Baere ◽  
Patrick Verschueren ◽  
René Westhovens ◽  
...  

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