PML Nuclear Body Component Sp140 Is a Novel Autoantigen in Primary Biliary Cirrhosis
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Granito, Alessandro
[1
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Yang, Wei-Hong
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Harvard Univ, Sch Med, Dept Med, Boston, MA USA
Massachusetts Gen Hosp, Gen Med Serv, Ctr Immunol & Inflammatory Dis, Boston, MA 02114 USAAlma Mater Studiorum Univ Bologna, Dipartimento Med Clin, I-40138 Bologna, Italy
Yang, Wei-Hong
[2
,3
]
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Muratori, Luigi
[1
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Lim, Mark J.
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AmberGen Inc, Watertown, MA USAAlma Mater Studiorum Univ Bologna, Dipartimento Med Clin, I-40138 Bologna, Italy
Lim, Mark J.
[4
]
Nakajima, Ayako
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Tokyo Womens Med Coll, Inst Rheumatol, Tokyo 162, JapanAlma Mater Studiorum Univ Bologna, Dipartimento Med Clin, I-40138 Bologna, Italy
Nakajima, Ayako
[5
]
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Ferri, Silvia
[1
]
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Pappas, Georgios
[1
]
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Quarneti, Chiara
[1
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Bianchi, Francesco B.
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Alma Mater Studiorum Univ Bologna, Dipartimento Med Clin, I-40138 Bologna, ItalyAlma Mater Studiorum Univ Bologna, Dipartimento Med Clin, I-40138 Bologna, Italy
Bianchi, Francesco B.
[1
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Bloch, Donald B.
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Harvard Univ, Sch Med, Dept Med, Boston, MA USA
Massachusetts Gen Hosp, Gen Med Serv, Ctr Immunol & Inflammatory Dis, Boston, MA 02114 USAAlma Mater Studiorum Univ Bologna, Dipartimento Med Clin, I-40138 Bologna, Italy
Bloch, Donald B.
[2
,3
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Muratori, Paolo
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Alma Mater Studiorum Univ Bologna, Dipartimento Med Clin, I-40138 Bologna, ItalyAlma Mater Studiorum Univ Bologna, Dipartimento Med Clin, I-40138 Bologna, Italy
Muratori, Paolo
[1
]
机构:
[1] Alma Mater Studiorum Univ Bologna, Dipartimento Med Clin, I-40138 Bologna, Italy
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[3] Massachusetts Gen Hosp, Gen Med Serv, Ctr Immunol & Inflammatory Dis, Boston, MA 02114 USA
[4] AmberGen Inc, Watertown, MA USA
[5] Tokyo Womens Med Coll, Inst Rheumatol, Tokyo 162, Japan
OBJECTIVES: Some patients with primary biliary cirrhosis (PBC) have antinuclear antibodies (ANAs). These ANAs include the "multiple nuclear dots" (MND) staining pattern, targeting promyelocytic leukemia protein (PML) nuclear body (NB) components, such as "speckled 100-kD" protein (Sp100) and PML. A new PML NB protein, designated as Sp140, was identified using serum from a PBC patient. The aim of this study was to analyze the immune response against Sp140 protein in PBC patients. METHODS: We studied 135 PBC patients and 157 pathological controls with type 1 autoimmune hepatitis, primary sclerosing cholangitis, and systemic lupus erythematosus. We used indirect immunofluorescence and a neuroblastoma cell line expressing Sp140 for detecting anti-Sp140 antibodies, and a commercially available immunoblot for detecting anti-Sp100 and anti-PML antibodies. RESULTS: Anti-Sp140 antibodies were present in 20 (15%) PBC patients but not in control samples, with a higher frequency in antimitochondrial antibody (AMA)-negative cases (53 vs. 9%, P<0.0001). Anti-Sp140 antibodies were found together with anti-Sp100 antibodies in all but one case (19 of 20, 90%) and with anti-PML antibodies in 12 (60%) cases. Anti-Sp140 positivity was not associated with a specific clinical feature of PBC. CONCLUSIONS: Our study identifies Sp140 as a new, highly specific autoantigen in PBC for the first time. The very frequent coexistence of anti-Sp140, anti-Sp100 and anti-PML antibodies suggests that the NB is a multiantigenic complex in PBC and enhances the diagnostic significance of these reactivities, which are particularly useful in AMA-negative cases.