CD4+ T cell depletion does not affect the level of viremia in chronically SHIVSF162P3N-infected Chinese cynomolgus monkeys

Chronically SHIVSF162P3N-infected cynomolgus monkeys were used to determine the effects of the antibody-mediated acute CD4+ T cell depletion on viral load as well as on the immunological factors associated with disease progression. Compared with the control animals, CD4+ T cell-depleted animals with...

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Veröffentlicht in:Virology (New York, N.Y.) N.Y.), 2021-08, Vol.560, p.76-85
Hauptverfasser: Liu, Hang, Liu, Jin-Biao, Meng, Feng-Zhen, Xu, Xi-Qiu, Wang, Yong, Xian, Qiao-Yang, Zhou, Run-Hong, Xiao, Qian-Hao, Huang, Zhi-Xiang, Zhou, Li, Li, Jie-Liang, Li, Xiang-Dong, Wang, Xu, Ho, Wen-Zhe, Zhuang, Ke
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Sprache:eng
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Zusammenfassung:Chronically SHIVSF162P3N-infected cynomolgus monkeys were used to determine the effects of the antibody-mediated acute CD4+ T cell depletion on viral load as well as on the immunological factors associated with disease progression. Compared with the control animals, CD4+ T cell-depleted animals with SHIV infection showed (i) little alteration in plasma viral load over the period of 22 weeks after the depletion; (ii) increased CD4+ T cell proliferation and turnover of macrophages at the early phase of the depletion, but subsequent decline to the basal levels; and (iii) little impact on the expression of the inflammatory cytokines and CC chemokines associated with disease progression. These findings indicate that the antibody-mediated acute CD4+ T cell depletion had minimal impact on plasma viral load and disease progression in chronically SHIVSF162P3N-infected cynomolgus monkeys. Future investigations are necessary to identify the key factor(s) related to the immune activation and macrophage infection during the CD4 deletion in chronic viral infection. •Antibody-mediated CD4+ T cell depletion in chronically SHIVSF162P3N-infected cynomolgus monkeys.•Determination of the effects of CD4+ T cell depletion on viral load and on the immunological factors.•Acute CD4+ T cell depletion had minimal impact on plasma viral load and disease progression.
ISSN:0042-6822
1096-0341
DOI:10.1016/j.virol.2021.04.012