Abstract |
We wished to confirm the staining pattern of HEp-2 cells by the anti Jo-1 antibody, because we found antibodies in serum with positive anti Jo-1 antibody which showed either a fibrilar cytoplasmic staining or a nuclear speckled staining pattern in indirect immuno fluorescence+ examinations using HEp-2 cells. Sera available from eight patients with PM DM ( polymyositis and/or dermatomyositis) showed positive anti Jo-1 antibody in the double immuno-diffusion technique but had various staining patterns of HEp-2 cells in the immunofluorescent examination. We examined these eight sera with the immuno-blotting method utilizing whole cell extract of HeLa cells, and found the 50 kDa band from all sera tested, to which Jo-1 antigen had been reported to move. We eluted the antibody which formed the 50 kDa band from the nitrocellulose membrane and applied it on HEp-2 cells. This maneuver gave us the fine granular cytoplasmic staining of anti Jo-1 antibody on HEp-2 cells. We therefore concluded that the anti Jo-1 antibody should have cytoplasmic staining on HEp-2 cells although observers might miss it due to other types of associated antinuclear antibodies.
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Authors | Y Nagano, S Yoshinoya, A Ohkubo |
Journal | Rinsho byori. The Japanese journal of clinical pathology
(Rinsho Byori)
Vol. 39
Issue 3
Pg. 269-72
(Mar 1991)
ISSN: 0047-1860 [Print] Japan |
PMID | 1711130
(Publication Type: English Abstract, Journal Article)
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Chemical References |
- Antibodies, Antinuclear
- Jo-1 antibody
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Topics |
- Antibodies, Antinuclear
(analysis)
- Cytoplasm
- Fluorescent Antibody Technique
- Humans
- Immunodiffusion
- Myositis
(diagnosis)
- Staining and Labeling
- Tumor Cells, Cultured
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