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Optimal therapeutic activity of monoclonal antibodies against chikungunya virus requires Fc-Fc?R interaction on monocytes.


ABSTRACT: Chikungunya virus (CHIKV) is an emerging mosquito-borne virus that has caused explosive outbreaks worldwide. Although neutralizing monoclonal antibodies (mAbs) against CHIKV inhibit infection in animals, the contribution of Fc effector functions to protection remains unknown. Here, we evaluated the activity of therapeutic mAbs that had or lacked the ability to engage complement and Fc? receptors (Fc?R). When administered as post-exposure therapy in mice, the Fc effector functions of mAbs promoted virus clearance from infected cells and reduced joint swelling-results that were corroborated in antibody-treated transgenic animals lacking activating Fc?R. The control of CHIKV infection by antibody-Fc?R engagement was associated with an accelerated influx of monocytes. A series of immune cell depletions revealed that therapeutic mAbs required monocytes for efficient clearance of CHIKV infection. Overall, our study suggests that in mice, Fc?R expression on monocytes is required for optimal therapeutic activity of antibodies against CHIKV and likely other related viruses.

SUBMITTER: Fox JM 

PROVIDER: S-EPMC6698136 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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Optimal therapeutic activity of monoclonal antibodies against chikungunya virus requires Fc-FcγR interaction on monocytes.

Fox Julie M JM   Roy Vicky V   Gunn Bronwyn M BM   Huang Ling L   Edeling Melissa A MA   Mack Matthias M   Fremont Daved H DH   Doranz Benjamin J BJ   Johnson Syd S   Alter Galit G   Diamond Michael S MS  

Science immunology 20190201 32


Chikungunya virus (CHIKV) is an emerging mosquito-borne virus that has caused explosive outbreaks worldwide. Although neutralizing monoclonal antibodies (mAbs) against CHIKV inhibit infection in animals, the contribution of Fc effector functions to protection remains unknown. Here, we evaluated the activity of therapeutic mAbs that had or lacked the ability to engage complement and Fcγ receptors (FcγR). When administered as post-exposure therapy in mice, the Fc effector functions of mAbs promote  ...[more]

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