Literature DB >> 17428313

Immunological research using RNA interference technology.

Chih-Ping Mao1, Yen-Yu Lin, Chien-Fu Hung, T-C Wu.   

Abstract

RNA interference (RNAi) is a potent method of gene silencing that has developed rapidly over the past few years as a result of its extensive importance in the study of genetics, molecular biology and physiology. RNAi technology has also recently yielded significant insight into the innate and adaptive immune systems by helping to elucidate numerous mechanisms that regulate the development, activation and function of cells that mediate immunity. In addition, because of its ability to suppress gene expression effectively, this technique may be used to regulate the immune response for clinical purposes. Nonetheless, before RNAi can be successfully administered into human patients as a medical treatment, it is necessary to overcome several major limitations of this technology, such as inefficient in vivo delivery, incomplete silencing of target genes, non-specific immune responses, and off-target effects. As novel developments and discoveries in molecular biology swiftly continue to unfold, it is likely that RNAi may soon translate into a potent form of in vivo gene silencing with profound applications to vaccination and immunotherapy. In the present review, we examine the current progress of immunological studies employing RNAi and discuss the prospects for the implementation of this technique in the clinical arena.

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Year:  2007        PMID: 17428313      PMCID: PMC2265953          DOI: 10.1111/j.1365-2567.2007.02599.x

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  87 in total

1.  Suppression of chemokine receptor expression by RNA interference allows for inhibition of HIV-1 replication.

Authors:  Miguel A Martínez; Arantxa Gutiérrez; Mercedes Armand-Ugón; Julià Blanco; Mariona Parera; Jordi Gómez; Bonaventura Clotet; José A Esté
Journal:  AIDS       Date:  2002-12-06       Impact factor: 4.177

2.  Poly(U) and polyadenylation termination signals are interchangeable for terminating the expression of shRNA from a pol II promoter.

Authors:  Jun Song; Shen Pang; Yingchun Lu; Robert Chiu
Journal:  Biochem Biophys Res Commun       Date:  2004-10-15       Impact factor: 3.575

Review 3.  The interface between innate and adaptive immunity.

Authors:  Kasper Hoebe; Edith Janssen; Bruce Beutler
Journal:  Nat Immunol       Date:  2004-10       Impact factor: 25.606

4.  Stable suppression of tumorigenicity by virus-mediated RNA interference.

Authors:  Thijn R Brummelkamp; René Bernards; Reuven Agami
Journal:  Cancer Cell       Date:  2002-09       Impact factor: 31.743

5.  Silencing of Bruton's tyrosine kinase (Btk) using short interfering RNA duplexes (siRNA).

Authors:  Juhana E Heinonen; C I Edvard Smith; Beston F Nore
Journal:  FEBS Lett       Date:  2002-09-11       Impact factor: 4.124

6.  Lentivirus-mediated RNA interference of DC-SIGN expression inhibits human immunodeficiency virus transmission from dendritic cells to T cells.

Authors:  Jean-François Arrighi; Marjorie Pion; Maciej Wiznerowicz; Teunis B Geijtenbeek; Eduardo Garcia; Shahnaz Abraham; Florence Leuba; Valérie Dutoit; Odile Ducrey-Rundquist; Yvette van Kooyk; Didier Trono; Vincent Piguet
Journal:  J Virol       Date:  2004-10       Impact factor: 5.103

7.  Activated human NK and CD8+ T cells express both TNF-related apoptosis-inducing ligand (TRAIL) and TRAIL receptors but are resistant to TRAIL-mediated cytotoxicity.

Authors:  Prisco Mirandola; Cristina Ponti; Giuliana Gobbi; Ivonne Sponzilli; Mauro Vaccarezza; Lucio Cocco; Giorgio Zauli; Paola Secchiero; Francesco Antonio Manzoli; Marco Vitale
Journal:  Blood       Date:  2004-06-17       Impact factor: 22.113

8.  Inhibiting HIV-1 infection in human T cells by lentiviral-mediated delivery of small interfering RNA against CCR5.

Authors:  Xiao-Feng Qin; Dong Sung An; Irvin S Y Chen; David Baltimore
Journal:  Proc Natl Acad Sci U S A       Date:  2002-12-23       Impact factor: 11.205

9.  Cleaving the oxidative repair protein Ape1 enhances cell death mediated by granzyme A.

Authors:  Zusen Fan; Paul J Beresford; Dong Zhang; Zhan Xu; Carl D Novina; Akira Yoshida; Yves Pommier; Judy Lieberman
Journal:  Nat Immunol       Date:  2003-01-13       Impact factor: 25.606

10.  RANKL-induced DC-STAMP is essential for osteoclastogenesis.

Authors:  Toshio Kukita; Naohisa Wada; Akiko Kukita; Takashi Kakimoto; Ferry Sandra; Kazuko Toh; Kengo Nagata; Tadahiko Iijima; Madoka Horiuchi; Hiromi Matsusaki; Kunio Hieshima; Osamu Yoshie; Hisayuki Nomiyama
Journal:  J Exp Med       Date:  2004-09-27       Impact factor: 14.307

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  2 in total

Review 1.  RNA interference: a potent technology in studying and modulating of dendritic cells, and potential in clinical therapy.

Authors:  Fang Cheng; Song He
Journal:  Mol Biol Rep       Date:  2009-09-12       Impact factor: 2.316

2.  A Unique Gene-Silencing Approach, Using an Intelligent RNA Expression Device (iRed), Results in Minimal Immune Stimulation When Given by Local Intrapleural Injection in Malignant Pleural Mesothelioma.

Authors:  Hidenori Ando; Noriko Saito-Tarashima; Amr S Abu Lila; Nozomi Kinjo; Taro Shimizu; Yu Ishima; Noriaki Minakawa; Tatsuhiro Ishida
Journal:  Molecules       Date:  2020-04-09       Impact factor: 4.411

  2 in total

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