Detection of High-Risk Paraneoplastic Antibodies against TRIM9 and TRIM67 Proteins

被引:7
|
作者
Bartley, Christopher M. [3 ,4 ]
Ngo, Thomas T. [3 ,4 ,5 ]
Do, Le Duy [6 ,7 ]
Zekeridou, Anastasia [8 ,9 ]
Dandekar, Ravi [3 ,5 ]
Muniz-Castrillo, Sergio [6 ,7 ]
Alvarenga, Bonny D. [3 ,5 ]
Zorn, Kelsey C. [10 ]
Tubati, Asritha [3 ,5 ]
Pinto, Anne-Laurie [6 ,7 ]
Browne, Weston D. [3 ,5 ]
Hullett, Patrick W. [3 ,5 ]
Terrelonge, Mark [3 ,5 ]
Schubert, Ryan D. [3 ,5 ]
Piquet, Amanda L. [11 ]
Yang, Binxia [9 ]
Montalvo, Mayra [8 ]
Kung, Andrew F. [12 ]
Mann, Sabrina A. [10 ,13 ]
Shah, Maulik P. [3 ,5 ]
Geschwind, Michael D. [3 ,5 ]
Gelfand, Jeffrey M. [3 ,5 ]
Derisi, Joseph L. [10 ,13 ]
Pittock, Sean J. [8 ,9 ]
Honnorat, Jerome [6 ,7 ]
Pleasure, Samuel J. [2 ,3 ,5 ]
Wilson, Michael R. [1 ,3 ,5 ]
机构
[1] Univ Calif San Francisco, Weill Inst Neurosci, 675 Nelson Rising Lane,NS212,Box 3206, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Weill Inst Neurosci, 675 Nelson Rising Lane,NS214,Box3206, San Francisco, CA 94158 USA
[3] Univ Calif San Francisco, Weill Inst Neurosci, San Francisco, CA USA
[4] Univ Calif San Francisco, Dept Psychiat & Behav Sci, San Francisco, CA USA
[5] Univ Calif San Francisco, Dept Neurol, San Francisco, CA USA
[6] Univ Claude Bernard Lyon 1, Univ Lyon, French Reference Ctr Paraneoplast Neurol Syndrome, Hosp Civils Lyon, Lyon, France
[7] Univ Claude Bernard Lyon 1, Univ Lyon, Inst Mech Integrated Life Sci, SynatAc Team,CNRS,INSERM,UMR 5284,U1314, Lyon, France
[8] Mayo Clin, Ctr Multiple Sclerosis & Autoimmune Neurol, Dept Neurol, Rochester, MN USA
[9] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN USA
[10] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA USA
[11] Univ Colorado Anschutz Med Campus, Sch Med, Dept Neurol, Aurora, CO USA
[12] Univ Calif San Francisco, Sch Med, PhD Degree Program Biol & Med Informat, San Francisco, CA USA
[13] Chan Zuckerberg Biohub, San Francisco, CA USA
关键词
OPSOCLONUS-MYOCLONUS SYNDROME; ANTI-YO ANTIBODIES; CEREBELLAR DEGENERATION; MELANOMA METASTASIS; LUNG-CANCER; AUTOANTIGEN; SECONDARY; PROLIFERATION; PROMOTES;
D O I
10.1002/ana.26776
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Co-occurring anti-tripartite motif-containing protein 9 and 67 autoantibodies (TRIM9/67-IgG) have been reported in only a very few cases of paraneoplastic cerebellar syndrome. The value of these biomarkers and the most sensitive methods of TRIM9/67-IgG detection are not known.Methods: We performed a retrospective, multicenter study to evaluate the cerebrospinal fluid and serum of candidate TRIM9/67-IgG cases by tissue-based immunofluorescence, peptide phage display immunoprecipitation sequencing, overexpression cell-based assay (CBA), and immunoblot. Cases in which TRIM9/67-IgG was detected by at least 2 assays were considered TRIM9/67-IgG positive.Results: Among these cases (n = 13), CBA was the most sensitive (100%) and revealed that all cases had TRIM9 and TRIM67 autoantibodies. Of TRIM9/67-IgG cases with available clinical history, a subacute cerebellar syndrome was the most common presentation (n = 7/10), followed by encephalitis (n = 3/10). Of these 10 patients, 70% had comorbid cancer (7/10), 85% of whom (n = 6/7) had confirmed metastatic disease. All evaluable cancer biopsies expressed TRIM9 protein (n = 5/5), whose expression was elevated in the cancerous regions of the tissue in 4 of 5 cases.Interpretation TRIM9/67-IgG is a rare but likely high-risk paraneoplastic biomarker for which CBA appears to be the most sensitive diagnostic assay. ANN NEUROL 2023
引用
收藏
页码:1086 / 1101
页数:16
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