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https://doi.org/10.1038/s41467-018-06227-9
Title: | Plasmodium co-infection protects against chikungunya virus-induced pathologies | Authors: | Teo, T.-H Lum, F.-M Ghaffar, K Chan, Y.-H Amrun, S.N Tan, J.J.L Lee, C.Y.P Chua, T.-K Carissimo, G Lee, W.W.L Claser, C Rajarethinam, R Rénia, L Ng, L.F.P |
Keywords: | chemokine receptor CXCR3 gamma interferon neutralizing antibody gamma interferon antibody apoptosis cell component chikungunya induced response infectious disease infiltration pathogen pathology virus animal experiment animal model antibody production apoptosis arthritis Article B lymphocyte CD4+ T lymphocyte cell maturation cell migration Chikungunya virus concurrent infection controlled study lymphocytic infiltration mixed infection mouse nonhuman Plasmodium spleen viral clearance viremia virus load animal C57BL mouse chikungunya Chikungunya virus female genetics human immunology knockout mouse malaria male metabolism mixed infection parasitology physiology Plasmodium virology Chikungunya virus Mus Animals Apoptosis Arthritis CD4-Positive T-Lymphocytes Chikungunya Fever Chikungunya virus Coinfection Female Humans Interferon-gamma Malaria Male Mice, Inbred C57BL Mice, Knockout Plasmodium Viral Load Viremia |
Issue Date: | 2018 | Publisher: | Nature Publishing Group | Citation: | Teo, T.-H, Lum, F.-M, Ghaffar, K, Chan, Y.-H, Amrun, S.N, Tan, J.J.L, Lee, C.Y.P, Chua, T.-K, Carissimo, G, Lee, W.W.L, Claser, C, Rajarethinam, R, Rénia, L, Ng, L.F.P (2018). Plasmodium co-infection protects against chikungunya virus-induced pathologies. Nature Communications 9 (1) : 3905. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-018-06227-9 | Abstract: | Co-infection with Plasmodium and chikungunya virus (CHIKV) has been reported in humans, but the impact of co-infection on pathogenesis remains unclear. Here, we show that prior exposure to Plasmodium suppresses CHIKV-associated pathologies in mice. Mechanistically, Plasmodium infection induces IFN?, which reduces viraemia of a subsequent CHIKV infection and suppresses tissue viral load and joint inflammation. Conversely, concomitant infection with both pathogens limits the peak of joint inflammation with no effect on CHIKV viraemia. Reduced peak joint inflammation is regulated by elevated apoptosis of CD4+ T-cells in the lymph nodes and disrupted CXCR3-mediated CD4+ T-cell migration that abolishes their infiltration into the joints. Virus clearance from tissues is delayed in both infection scenarios, and is associated with a disruption of B cell affinity-maturation in the spleen that reduces CHIKV-neutralizing antibody production. © 2018, The Author(s). | Source Title: | Nature Communications | URI: | https://scholarbank.nus.edu.sg/handle/10635/174206 | ISSN: | 2041-1723 | DOI: | 10.1038/s41467-018-06227-9 |
Appears in Collections: | Elements Staff Publications |
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