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A’la, R., Ernawati, R., Retno L, N. D., Mufasirin, M., Ma’ruf, A., & Rantam, F. A. (2017). Construction Hybrid immunoglobulin All Four Dengue serotype Using Mesenchymal Stem. KnE Life Sciences, 3(6), 520-527. https://doi.org/10.18502/kls.v3i6.1178

https://doi.org/10.18502/kls.v3i6.1178

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authors

  • Rofiqul A’la

    Rofiqul A’la

    Master student of Vaccine and Immunotherapeutics Faculty of Veterinary Medicine, Airlangga University, Surabaya 60286
  • Rahaju Ernawati

    Rahaju Ernawati

    Microbiology Departement Faculty of Veterinary Medicine,Airlangga University, Surabaya 60286
  • Nunuk Dyah Retno L

    Nunuk Dyah Retno L

    Parasitology Departement Faculty of Veterinary Medicine, Airlangga University, Surabaya 60286
  • Mufasirin Mufasirin

    Mufasirin Mufasirin

    Parasitology Departement Faculty of Veterinary Medicine, Airlangga University, Surabaya 60286
  • Anwar Ma’ruf

    Anwar Ma’ruf

    Basic veterinary medicine departement Faculty of Veterinary Medicine, Airlangga University, Surabaya 60286
  • Fedik A. Rantam

    Fedik A. Rantam

    Microbiology Department Faculty of Veterinary Medicine, Airlangga University, Surabaya 60286 Stem Cell development and research, Airlangga University, Surabaya 60286

Published Date

  • Dec 3, 2017

Construction Hybrid immunoglobulin All Four Dengue serotype Using Mesenchymal Stem

KnE Life Sciences / The Veterinary Medicine International Conference (VMIC) / Pages 520-527

Abstract

The dengue virus is a member of vector-borne diseases that causes zoonotic disease and spreads rapidly in the world. No single treatment or vaccine yet is available that is recommended and there is no correlation with protectiveness against this disease. The heavy chain (VH) and light chain (VL) variables are molecules of immunoglobulin G (IgG) is the smallest part of the antibody. Although the part-time domain variable is short, it can be used as a long-term and rapid immune booster in the immune system. In this study we tried to clone an encoding gene that was able to influence the adaptive immune response to dengue 1-4 by using MSC as a gene carrier. The target scFv-IgG gene has been successfully integrated into the plasmid. Plasmids that we have linearly transfected into the MSC. From the cDNA synthesis results continued with PCR synthesis with primer FGHV and RGHA obtained bands in accordance with the target of 404 bp. The scFv gene encoding IgG can be integrated with MSC

Keywords: immunetherapy; dengue; hybrid; scFv-IgG; mesenchymal 

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