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CD4+ and CD8+ T cells are not the main driver of Lassa fever pathogenesis in macaques
Jérémie Prévost, Nikesh Tailor, Geoff Soule, Jonathan Audet, Yvon Deschambault, Robert Vendramelli, Jessica Prado-Smith, Kevin Tierney, Kimberly Azaransky, Darwyn Kobasa, Chad S. Clancy, Heinz Feldmann, Kyle Rosenke, David Safronetz
Jérémie Prévost, Nikesh Tailor, Geoff Soule, Jonathan Audet, Yvon Deschambault, Robert Vendramelli, Jessica Prado-Smith, Kevin Tierney, Kimberly Azaransky, Darwyn Kobasa, Chad S. Clancy, Heinz Feldmann, Kyle Rosenke, David Safronetz
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Research Article Microbiology Public Health Virology

CD4+ and CD8+ T cells are not the main driver of Lassa fever pathogenesis in macaques

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Abstract

Empirical data from survivors of Lassa fever and experimental disease modeling efforts, particularly those using mouse models, are at odds with respect to T cell–mediated pathogenesis. In mice, T cells have been shown to be imperative in disease progression and lethality, whereas in humans, an early and robust T cell response has been associated with survival. Here, we assessed the role of CD4+ and CD8+ T cells on disease progression and severity of Lassa virus infection in a nonhuman primate model. Using an antibody-mediated T cell depletion strategy prior to and after inoculation, we were able to examine Lassa virus infection in the absence of specific T cell responses. In animals depleted for either CD4+ or CD8+ T cells, Lassa virus infection remained uniformly lethal, with only a slight delay in disease progression was observed in the CD4-depleted group when compared with nondepleted controls. Milder pulmonary pathology was noticed in the absence of CD4+ or CD8+ T cells. Overall, our findings suggest that T cells have a limited effect on the development of Lassa fever in nonhuman primates.

Authors

Jérémie Prévost, Nikesh Tailor, Geoff Soule, Jonathan Audet, Yvon Deschambault, Robert Vendramelli, Jessica Prado-Smith, Kevin Tierney, Kimberly Azaransky, Darwyn Kobasa, Chad S. Clancy, Heinz Feldmann, Kyle Rosenke, David Safronetz

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Figure 4

Hematological and coagulation parameters of T cell–depleted LASV-infected cynomolgus macaques.

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Hematological and coagulation parameters of T cell–depleted LASV-infecte...
(A–L) EDTA-treated blood samples collected from NHPs at regular intervals before and after infection were monitored for absolute counts of white blood cells (A), red blood cells (B), platelets (C), neutrophils (D), eosinophils (E), basophils (F), monocytes (G), and lymphocytes (H) using a HM5 hematology analyzer. (I–L) Lymphocyte populations (B cells, T cells, NK cells, NKT cells) were monitored by flow cytometry. (M–P) Citrate plasma obtained from NHP blood samples were monitored for prothrombin (M), activated partial thromboplastin (N), and fibrinogen (O) using the Satellite Max analyzer, as well as D-dimer by ELISA (P). Data are represented as connecting lines for each individual animal. Where available, normal ranges are indicated by gray shading area (56).

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