Literature DB >> 25758251

Antiviral antibody profiling by high-density protein arrays.

Xiaofang Bian1, Peter Wiktor2, Peter Kahn3, Al Brunner3, Amritpal Khela1, Kailash Karthikeyan1, Kristi Barker1, Xiaobo Yu1, Mitch Magee1, Clive H Wasserfall4, David Gibson5, Madeleine E Rooney6, Ji Qiu1, Joshua LaBaer1.   

Abstract

Viral infections elicit antiviral antibodies and have been associated with various chronic diseases. Detection of these antibodies can facilitate diagnosis, treatment of infection, and understanding of the mechanisms of virus-associated diseases. In this work, we assayed antiviral antibodies using a novel high-density nucleic acid programmable protein array (HD-NAPPA) platform. Individual viral proteins were expressed in situ directly from plasmids encoding proteins in an array of microscopic reaction chambers. Quality of protein display and serum response was assured by comparing intra- and inter-array correlation within or between printing batches with average correlation coefficients of 0.91 and 0.96, respectively. HD-NAPPA showed higher signal-to-background ratio compared with standard NAPPA on planar glass slides and ELISA. Antibody responses to 761 antigens from 25 different viruses were profiled among patients with juvenile idiopathic arthritis and type 1 diabetes. Common and unique antibody reactivity patterns were detected between patients and healthy controls. We believe HD-viral-NAPPA will enable the study of host-pathogen interactions at unprecedented dimensions and elucidate the role of pathogen infections in disease development.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Antiviral antibodies; HD-NAPPA; Juvenile idiopathic arthritis; Protein arrays; Type 1 diabetes

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Substances:

Year:  2015        PMID: 25758251      PMCID: PMC4545592          DOI: 10.1002/pmic.201400612

Source DB:  PubMed          Journal:  Proteomics        ISSN: 1615-9853            Impact factor:   3.984


  39 in total

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Review 2.  Juvenile idiopathic arthritis.

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4.  Human parvovirus B19 DNA in synovial fluid.

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6.  Application of virus-specific immunoglobulin M (IgM), IgG, and IgA antibody detection with a polyantigenic enzyme-linked immunosorbent assay for diagnosis of Epstein-Barr virus infections in childhood.

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Journal:  J Clin Microbiol       Date:  2001-11       Impact factor: 5.948

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Journal:  Clin Microbiol Rev       Date:  2011-01       Impact factor: 26.132

8.  Autoantigen microarrays for multiplex characterization of autoantibody responses.

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Journal:  Nat Med       Date:  2002-03       Impact factor: 53.440

9.  Coxsackie B, mumps, rubella, and cytomegalovirus specific IgM responses in patients with juvenile-onset insulin-dependent diabetes mellitus in Britain, Austria, and Australia.

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Journal:  Lancet       Date:  1985-06-22       Impact factor: 79.321

10.  Viral antibodies in diabetes mellitus.

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Journal:  Br Med J       Date:  1969-09-13
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3.  Nucleic Acid Programmable Protein Arrays (NAPPA) for the Discovery of Autoantibodies in Osteoarthritis.

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4.  A Contra Capture Protein Array Platform for Studying Post-translationally Modified (PTM) Auto-antigenomes.

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Journal:  Mol Cell Proteomics       Date:  2016-05-02       Impact factor: 5.911

Review 5.  Variability in Humoral Immunity to Measles Vaccine: New Developments.

Authors:  Iana H Haralambieva; Richard B Kennedy; Inna G Ovsyannikova; Jennifer A Whitaker; Gregory A Poland
Journal:  Trends Mol Med       Date:  2015-11-18       Impact factor: 11.951

Review 6.  Proteomics and integrative omic approaches for understanding host-pathogen interactions and infectious diseases.

Authors:  Pierre M Jean Beltran; Joel D Federspiel; Xinlei Sheng; Ileana M Cristea
Journal:  Mol Syst Biol       Date:  2017-03-27       Impact factor: 11.429

Review 7.  Proteomic approaches to uncovering virus-host protein interactions during the progression of viral infection.

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Journal:  Expert Rev Proteomics       Date:  2016       Impact factor: 3.940

8.  Multiplexed Nucleic Acid Programmable Protein Arrays.

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Review 9.  Advancing translational research with next-generation protein microarrays.

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