Literature DB >> 28269795

SMN Blood Levels in a Porcine Model of Spinal Muscular Atrophy.

Chitra Iyer1, Xueqian Wang1, Samantha R Renusch1, Sandra I Duque1, Allison M Wehr2, Xiaokui-Molly Mo2, Vicki L McGovern1, W David Arnold3,4, Arthur H M Burghes1, Stephen J Kolb1,3.   

Abstract

BACKGROUND: Spinal Muscular Atrophy (SMA) is an autosomal recessive motor neuron disease that results in loss of spinal motor neurons, muscular weakness and, in severe cases, respiratory failure and death. SMA is caused by a deletion or mutation of the SMN1 gene and retention of the SMN2 gene that leads to low SMN expression levels.The measurement of SMN mRNA levels in peripheral blood samples has been used in SMA clinical studies as a pharmacodynamic biomarker for response to therapies designed to increase SMN levels. We recently developed a postnatal porcine model of SMA by the viral delivery of a short-hairpin RNA (shRNA) targeting porcine SMN (pSMN). scAAV9-mediated knockdown of pSMN mRNA at postnatal day 5 results in denervation, weakness and motor neuron and ventral root axon loss that begins 3-4 weeks after viral delivery, and this phenotype can be ameliorated by subsequent viral delivery of human SMN (hSMN).
OBJECTIVE: To determine if the effect of modulating SMN levels using gene therapy can be measured in blood.
METHODS: We measured expression of pSMN mRNA and hSMN mRNA by quantitative droplet digital PCR (ddPCR).
RESULTS: We found that the endogenous expression of pSMN mRNA in blood increases in the first month of life. However, there were no significant differences in blood levels of pSMN mRNA after knock-down or of human SMN mRNA after gene therapy.
CONCLUSIONS: Our results, obtained in a large animal model of SMA that is similar in size and anatomy to human infants, suggest that measurement of SMN mRNA levels in blood may not be informative in SMA clinical trials involving intrathecal delivery of SMN-modulating therapies.

Entities:  

Keywords:  SMA; SMN; ddPCR; gene-therapy; scAAV9-SMN; scAAV9-shRNA

Mesh:

Substances:

Year:  2017        PMID: 28269795      PMCID: PMC5531281          DOI: 10.3233/JND-170209

Source DB:  PubMed          Journal:  J Neuromuscul Dis


  24 in total

1.  Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study.

Authors:  Francesco D Tiziano; Rosa Lomastro; Lorena Di Pietro; Maria Barbara Pasanisi; Stefania Fiori; Carla Angelozzi; Emanuela Abiusi; Corrado Angelini; Gianni Sorarù; Alessandra Gaiani; Tiziana Mongini; Liliana Vercelli; Gessica Vasco; Giuseppe Vita; Gian Luca Vita; Sonia Messina; Luisa Politano; Luigia Passamano; Grazia Di Gregorio; Cristina Montomoli; Chiara Orsi; Angela Campanella; Renato Mantegazza; Lucia Morandi
Journal:  Eur J Hum Genet       Date:  2012-10-17       Impact factor: 4.246

2.  Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number.

Authors:  P E McAndrew; D W Parsons; L R Simard; C Rochette; P N Ray; J R Mendell; T W Prior; A H Burghes
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

3.  The gene frequency of acute Werdnig-Hoffmann disease (SMA type 1). A total population survey in North-East England.

Authors:  J H Pearn
Journal:  J Med Genet       Date:  1973-09       Impact factor: 6.318

4.  In vivo activation of SMN in spinal muscular atrophy carriers and patients treated with valproate.

Authors:  Lars Brichta; Irmgard Holker; Karsten Haug; Thomas Klockgether; Brunhilde Wirth
Journal:  Ann Neurol       Date:  2006-06       Impact factor: 10.422

5.  Improving single injection CSF delivery of AAV9-mediated gene therapy for SMA: a dose-response study in mice and nonhuman primates.

Authors:  Kathrin Meyer; Laura Ferraiuolo; Leah Schmelzer; Lyndsey Braun; Vicki McGovern; Shibi Likhite; Olivia Michels; Alessandra Govoni; Julie Fitzgerald; Pablo Morales; Kevin D Foust; Jerry R Mendell; Arthur H M Burghes; Brian K Kaspar
Journal:  Mol Ther       Date:  2014-10-31       Impact factor: 11.454

6.  A large animal model of spinal muscular atrophy and correction of phenotype.

Authors:  Sandra I Duque; W David Arnold; Philipp Odermatt; Xiaohui Li; Paul N Porensky; Leah Schmelzer; Kathrin Meyer; Stephen J Kolb; Daniel Schümperli; Brian K Kaspar; Arthur H M Burghes
Journal:  Ann Neurol       Date:  2015-02-09       Impact factor: 10.422

7.  SMN mRNA and protein levels in peripheral blood: biomarkers for SMA clinical trials.

Authors:  C J Sumner; S J Kolb; G G Harmison; N O Jeffries; K Schadt; R S Finkel; G Dreyfuss; K H Fischbeck
Journal:  Neurology       Date:  2006-02-15       Impact factor: 9.910

8.  Molecular analysis of spinal muscular atrophy and modification of the phenotype by SMN2.

Authors:  Matthew D Mailman; John W Heinz; Audrey C Papp; Pamela J Snyder; Mary S Sedra; Brunhilde Wirth; Arthur H M Burghes; Thomas W Prior
Journal:  Genet Med       Date:  2002 Jan-Feb       Impact factor: 8.822

9.  Baseline results of the NeuroNEXT spinal muscular atrophy infant biomarker study.

Authors:  Stephen J Kolb; Christopher S Coffey; Jon W Yankey; Kristin Krosschell; W David Arnold; Seward B Rutkove; Kathryn J Swoboda; Sandra P Reyna; Ai Sakonju; Basil T Darras; Richard Shell; Nancy Kuntz; Diana Castro; Susan T Iannaccone; Julie Parsons; Anne M Connolly; Claudia A Chiriboga; Craig McDonald; W Bryan Burnette; Klaus Werner; Mathula Thangarajh; Perry B Shieh; Erika Finanger; Merit E Cudkowicz; Michelle M McGovern; D Elizabeth McNeil; Richard Finkel; Edward Kaye; Allison Kingsley; Samantha R Renusch; Vicki L McGovern; Xueqian Wang; Phillip G Zaworski; Thomas W Prior; Arthur H M Burghes; Amy Bartlett; John T Kissel
Journal:  Ann Clin Transl Neurol       Date:  2016-01-21       Impact factor: 4.511

10.  SMN Protein Can Be Reliably Measured in Whole Blood with an Electrochemiluminescence (ECL) Immunoassay: Implications for Clinical Trials.

Authors:  Phillip Zaworski; Katharine M von Herrmann; Shannon Taylor; Sara S Sunshine; Kathleen McCarthy; Nicole Risher; Tara Newcomb; Marla Weetall; Thomas W Prior; Kathryn J Swoboda; Karen S Chen; Sergey Paushkin
Journal:  PLoS One       Date:  2016-03-08       Impact factor: 3.240

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  3 in total

1.  Natural history of infantile-onset spinal muscular atrophy.

Authors:  Stephen J Kolb; Christopher S Coffey; Jon W Yankey; Kristin Krosschell; W David Arnold; Seward B Rutkove; Kathryn J Swoboda; Sandra P Reyna; Ai Sakonju; Basil T Darras; Richard Shell; Nancy Kuntz; Diana Castro; Julie Parsons; Anne M Connolly; Claudia A Chiriboga; Craig McDonald; W Bryan Burnette; Klaus Werner; Mathula Thangarajh; Perry B Shieh; Erika Finanger; Merit E Cudkowicz; Michelle M McGovern; D Elizabeth McNeil; Richard Finkel; Susan T Iannaccone; Edward Kaye; Allison Kingsley; Samantha R Renusch; Vicki L McGovern; Xueqian Wang; Phillip G Zaworski; Thomas W Prior; Arthur H M Burghes; Amy Bartlett; John T Kissel
Journal:  Ann Neurol       Date:  2017-12-08       Impact factor: 10.422

Review 2.  Recognising the potential of large animals for modelling neuromuscular junction physiology and disease.

Authors:  Stephen D Cahalan; Ines Boehm; Ross A Jones; Richard J Piercy
Journal:  J Anat       Date:  2022-09-02       Impact factor: 2.921

3.  Evaluation of potential effects of Plastin 3 overexpression and low-dose SMN-antisense oligonucleotides on putative biomarkers in spinal muscular atrophy mice.

Authors:  Eike A Strathmann; Miriam Peters; Seyyedmohsen Hosseinibarkooie; Frank W Rigo; C Frank Bennett; Phillip G Zaworski; Karen S Chen; Michael Nothnagel; Brunhilde Wirth
Journal:  PLoS One       Date:  2018-09-06       Impact factor: 3.240

  3 in total

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