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[Minireview] Primary lymphocyte infection models for KSHV and its putative tumorigenesis mechanisms in B cell lymphomas
Sangmin Kang , Jinjong Myoung
J. Microbiol. 2017;55(5):319-329.   Published online April 29, 2017
DOI: https://doi.org/10.1007/s12275-017-7075-2
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  • 12 Crossref
AbstractAbstract
Kaposi’s sarcoma-associated herpesvirus (KSHV) is the latest addition to the human herpesvirus family. Unlike alpha- and beta-herpesvirus subfamily members, gamma-herpesviruses, including Epstein-Barr virus (EBV) and KSHV, cause vari-ous tumors in humans. KSHV primarily infects endothelial and B cells in vivo, and is associated with at least three malig-nancies: Kaposi’s sarcoma and two B cell lymphomas, res-pectively. Although KSHV readily infects endothelial cells in vitro and thus its pathogenic mechanisms have been exten-sively studied, B cells had been refractory to KSHV infection. As such, functions of KSHV genes have mostly been eluci-dated in endothelial cells in the context of viral infection but not in B cells. Whether KSHV oncogenes, defined in endo-thelial cells, play the same roles in the tumorigenesis of B cells remains an open question. Only recently, through a few ground-breaking studies, B cell infection models have been established. In this review, those models will be compared and contrasted and putative mechanisms of KSHV-induced B cell transformation will be discussed.

Citations

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  • Folate-Targeted Nanocarriers Co-Deliver Ganciclovir and miR-34a-5p for Combined Anti-KSHV Therapy
    Fangling Li, Dongdong Cao, Wenyi Gu, Dongmei Li, Zhiyong Liu, Lin Cui
    International Journal of Molecular Sciences.2024; 25(5): 2932.     CrossRef
  • Structural aspects of hepatitis E virus
    Florencia Cancela, Ofelia Noceti, Juan Arbiza, Santiago Mirazo
    Archives of Virology.2022; 167(12): 2457.     CrossRef
  • iTIME.219: An Immortalized KSHV Infected Endothelial Cell Line Inducible by a KSHV-Specific Stimulus to Transition From Latency to Lytic Replication and Infectious Virus Release
    Stephen J. Dollery, Tania D. Maldonado, Eric A. Brenner, Edward A. Berger
    Frontiers in Cellular and Infection Microbiology.2021;[Epub]     CrossRef
  • Analysis of KSHV B lymphocyte lineage tropism in human tonsil reveals efficient infection of CD138+ plasma cells
    Farizeh Aalam, Romina Nabiee, Jesus Ramirez Castano, Jennifer Totonchy, Vera L. Tarakanova
    PLOS Pathogens.2020; 16(10): e1008968.     CrossRef
  • Molecular Virology of KSHV in the Lymphocyte Compartment—Insights From Patient Samples and De Novo Infection Models
    Farizeh Aalam, Jennifer Totonchy
    Frontiers in Cellular and Infection Microbiology.2020;[Epub]     CrossRef
  • Molecular and cellular interplay in virus-induced tumors in solid organ recipients
    Alessia Gallo, Monica Miele, Ester Badami, Pier Giulio Conaldi
    Cellular Immunology.2019; 343: 103770.     CrossRef
  • Middle East respiratory syndrome coronavirus-encoded ORF8b strongly antagonizes IFN-β promoter activation: its implication for vaccine design
    Jeong Yoon Lee, Sojung Bae, Jinjong Myoung
    Journal of Microbiology.2019; 57(9): 803.     CrossRef
  • Methyltransferase of a cell culture-adapted hepatitis E inhibits the MDA5 receptor signaling pathway
    Jinjong Myoung, Jeong Yoon Lee, Kang Sang Min
    Journal of Microbiology.2019; 57(12): 1126.     CrossRef
  • Cell Type-Specific Interferon-γ-mediated Antagonism of KSHV Lytic Replication
    Mi-Kyung Park, Hyejeong Cho, Seong Woon Roh, Seong-Jun Kim, Jinjong Myoung
    Scientific Reports.2019;[Epub]     CrossRef
  • Comment on primary lymphocyte infection models for KSHV and its putative tumorigenesis mechanisms in B cell lymphomas (Journal of Microbiology 2017, 55(5): 319-329)
    Giovanna Rappocciolo, Frank Jenkins, Charles R. Rinaldo
    Journal of Microbiology.2017; 55(7): 592.     CrossRef
  • Lipids, lipid metabolism and Kaposi’s sarcoma-associated herpesvirus pathogenesis
    Lu Dai, Zhen Lin, Wei Jiang, Erik K. Flemington, Zhiqiang Qin
    Virologica Sinica.2017; 32(5): 369.     CrossRef
  • The Roles of Matricellular Proteins in Oncogenic Virus-Induced Cancers and Their Potential Utilities as Therapeutic Targets
    Naoyoshi Maeda, Katsumi Maenaka
    International Journal of Molecular Sciences.2017; 18(10): 2198.     CrossRef
Research Support, Non-U.S. Gov't
Comparative Analysis of Immune Responses to Mycobacterium abscessus Infection and Its Antigens in Two Murine Models
Bo-Young Jeon , Jeongyeon Kwak , Seung-Sub Lee , SangNae Cho , Chul Jae Won , Jin Man Kim , Sung Jae Shin
J. Microbiol. 2009;47(5):633-640.   Published online October 24, 2009
DOI: https://doi.org/10.1007/s12275-009-0139-1
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  • 10 Crossref
AbstractAbstract
Mycobacterium abscessus has been identified as an emerging pulmonary pathogen in humans. Because little is known regarding immune responses elicited by M. abscessus or its antigens, immunological responses were studied in two murine models subjected to intravenous (high-dose or systemic infection) or pulmonary (low-dose or local infection) inoculation with M. abscessus ATCC 19977. An overall comparison between the two models showed similar patterns of bacterial survival and host immune responses. The colonization of M. abscessus was the highest at 5 days post-infection (dpi) and its elimination was positively correlated with cell-mediated immunity in both challenges. However, an inverse relationship was observed between progressive inflammation and mycobacterial colonization levels in mice infected with a high dose at 14 dpi. Regarding antigens, culture filtrate (CF) of M. abscessus strongly induced IFN-γ secretion, whereas cellular extract (CE) antigen elicited strong antibody responses. The antibody response to M. abscessus antigens in mice subjected to low-dose infection increased when the cellular immune response decreased over 14 dpi. However, the antibody response for the high-dose infection increased promptly after the infection. In comparison of cytokine expression in lung homogenates after M. abscessus infection, Th1 and Th2 cytokines increased simultaneously in the high-dose infection, whereas only cell-mediated immunity developed in the low-dose pulmonary infection. These findings not only enhance our understanding of the immune response to M. abscessus infection according to systemic or pulmonary infection, but may also aid in immunological diagnosis and vaccine development.

Citations

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  • Mycobacterium abscessus biofilm cleared from murine lung by monoclonal antibody against bacterial DNABII proteins
    Joseph A. Jurcisek, Nikola Kurbatfinski, Kathryn Q. Wilbanks, Jaime D. Rhodes, Steven D. Goodman, Lauren O. Bakaletz
    Journal of Cystic Fibrosis.2025; 24(2): 374.     CrossRef
  • Virulence Mechanisms of Mycobacterium abscessus: Current Knowledge and Implications for Vaccine Design
    Kia C. Ferrell, Matt D. Johansen, James A. Triccas, Claudio Counoupas
    Frontiers in Microbiology.2022;[Epub]     CrossRef
  • Vaccination inducing durable and robust antigen-specific Th1/Th17 immune responses contributes to prophylactic protection against Mycobacterium avium infection but is ineffective as an adjunct to antibiotic treatment in chronic disease
    Ju Mi Lee, Jiyun Park, Steven G Reed, Rhea N Coler, Jung Joo Hong, Lee-Han Kim, Wonsik Lee, Kee Woong Kwon, Sung Jae Shin
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  • Species-Specific Interferon-Gamma Release Assay for the Diagnosis of Mycobacterium abscessus Complex Infection
    Mathis Steindor, Florian Stehling, Margarete Olivier, Jan Kehrmann, Margo Diricks, Florian P. Maurer, Peter A. Horn, Svenja Straßburg, Matthias Welsner, Sivagurunathan Sutharsan, Monika Lindemann
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    Ophir Bar-On, Huda Mussaffi, Meir Mei-Zahav, Dario Prais, Guy Steuer, Patrick Stafler, Shai Hananya, Hannah Blau
    Journal of Cystic Fibrosis.2015; 14(1): 53.     CrossRef
  • Differential Immune Responses to Segniliparus rotundus and Segniliparus rugosus Infection and Analysis of Their Comparative Virulence Profiles
    Jong-Seok Kim, Woo Sik Kim, Keehoon Lee, Choul-Jae Won, Jin Man Kim, Seok-Yong Eum, Won-Jung Koh, Sung Jae Shin, Yung-Fu Chang
    PLoS ONE.2013; 8(3): e59646.     CrossRef
  • Mycobacterium abscessus Bacteremia After Receipt of Intravenous Infusate of Cytokine-Induced Killer Cell Therapy for Body Beautification and Health Boosting
    Raymond Liu, Kelvin K. W. To, Jade L. L. Teng, Garnet K. Y. Choi, Ka-Yi Mok, Kin-Ip Law, Eugene Y. K. Tso, Kitty S. C. Fung, Tak-Chiu Wu, Alan K. L. Wu, Shing-Hoi Fung, Sally C. Y. Wong, Nigel J. Trendell-Smith, Kwok-Yung Yuen
    Clinical Infectious Diseases.2013; 57(7): 981.     CrossRef
  • Current Understanding ofMycobacterium abscessusInfection
    Go-Eun Choi, Youngsuk Jo, Sung Jae Shin
    Journal of Bacteriology and Virology.2012; 42(1): 17.     CrossRef

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