Literature DB >> 27153814

CD55 is a key complement regulatory protein that counteracts complement-mediated inactivation of Newcastle Disease Virus.

Udaya S Rangaswamy1, Christopher R Cotter1, Xing Cheng1, Hong Jin1, Zhongying Chen1.   

Abstract

Newcastle disease virus (NDV) is being developed as an oncolytic virus for virotherapy. In this study we analysed the regulation of complement-mediated inactivation of a recombinant NDV in different host cells. NDV grown in human cells was less sensitive to complement-mediated virus inactivation than NDV grown in embryonated chicken eggs. Additionally, NDV produced from HeLa-S3 cells is more resistant to complement than NDV from 293F cells, which correlated with higher expression and incorporation of complement regulatory proteins (CD46, CD55 and CD59) into virions from HeLa-S3 cells. Further analysis of the recombinant NDVs individually expressing the three CD molecules showed that CD55 is the most potent in counteracting complement-mediated virus inactivation. The results provide important information on selecting NDV manufacture substrate to mitigate complement-mediated virus inactivation.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 27153814     DOI: 10.1099/jgv.0.000498

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  8 in total

Review 1.  Interactions of viruses and the humoral innate immune response.

Authors:  Bailey E Maloney; Krishani Dinali Perera; Danielle R D Saunders; Naemi Shadipeni; Sherry D Fleming
Journal:  Clin Immunol       Date:  2020-02-04       Impact factor: 3.969

2.  CD59 association with infectious bronchitis virus particles protects against antibody-dependent complement-mediated lysis.

Authors:  Yanquan Wei; Yanhong Ji; Huichen Guo; Xiaoying Zhi; Shichong Han; Yun Zhang; Yuan Gao; Yanyan Chang; Dan Yan; Kangyu Li; Ding Xiang Liu; Shiqi Sun
Journal:  J Gen Virol       Date:  2017-10-25       Impact factor: 3.891

3.  Ionic Strength-Dependent, Reversible Pleomorphism of Recombinant Newcastle Disease Virus.

Authors:  Benjamin S Rush; Matieyendou Didier Djagbare; Jeffrey A Speir; Gautam Sanyal
Journal:  J Virol       Date:  2020-10-27       Impact factor: 5.103

4.  Systemic cancer therapy with engineered adenovirus that evades innate immunity.

Authors:  Svetlana Atasheva; Corey C Emerson; Jia Yao; Cedrick Young; Phoebe L Stewart; Dmitry M Shayakhmetov
Journal:  Sci Transl Med       Date:  2020-11-25       Impact factor: 19.319

5.  Caveolae provide a specialized membrane environment for respiratory syncytial virus assembly.

Authors:  Alexander Ludwig; Tra Huong Nguyen; Daniel Leong; Laxmi Iyer Ravi; Boon Huan Tan; Sara Sandin; Richard J Sugrue
Journal:  J Cell Sci       Date:  2017-02-02       Impact factor: 5.285

Review 6.  Relating GPI-Anchored Ly6 Proteins uPAR and CD59 to Viral Infection.

Authors:  Jingyou Yu; Vaibhav Murthy; Shan-Lu Liu
Journal:  Viruses       Date:  2019-11-14       Impact factor: 5.048

Review 7.  Emerging systemic delivery strategies of oncolytic viruses: A key step toward cancer immunotherapy.

Authors:  Weiyue Ban; Jianhuan Guan; Hanwei Huang; Zhonggui He; Mengchi Sun; Funan Liu; Jin Sun
Journal:  Nano Res       Date:  2022-02-14       Impact factor: 10.269

8.  Comparison between intratumoral and intravenously administered oncolytic virus therapy with Newcastle disease virus in a xenograft murine model for pancreatic adenocarcinoma.

Authors:  J Fréderique de Graaf; Marco Huberts; Daphne Groeneveld; Stefan van Nieuwkoop; Casper H J van Eijck; Ron A M Fouchier; Bernadette G van den Hoogen
Journal:  Heliyon       Date:  2022-07-09
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.