In-vitro evaluation of the immunomodulatory effects of Baricitinib: Implication for COVID-19 therapy

被引:43
作者
Petrone, Linda [1 ]
Petruccioli, Elisa [1 ]
Alonzi, Tonino [1 ]
Vanini, Valentina [1 ]
Cuzzi, Gilda [1 ]
Fard, Saeid Najafi [1 ]
Castilletti, Concetta [2 ]
Palmieri, Fabrizio [3 ]
Gualano, Gina [3 ]
Vittozzi, Pietro [3 ]
Nicastri, Emanuele [4 ]
Lepore, Luciana [4 ]
Grifoni, Alba [5 ]
Antinori, Andrea [6 ]
Vergori, Alessandra [6 ]
Ippolito, Giuseppe [7 ]
Cantini, Fabrizio [8 ]
Goletti, Delia [1 ]
机构
[1] Natl Inst Infect Dis Lazzaro Spallanzani IRCCS, Translat Res Unit, Rome, Italy
[2] Natl Inst Infect Dis Lazzaro Spallanzani IRCCS, Virol Lab, Rome, Italy
[3] Natl Inst Infect Dis Lazzaro Spallanzani IRCCS, Resp Infect Dis Unit, Rome, Italy
[4] Natl Inst Infect Dis Lazzaro Spallanzani IRCCS, Clin Div Infect Dis, Rome, Italy
[5] La Jolla Inst Immunol LJI, Ctr Infect Dis & Vaccine Res, La Jolla, CA 92037 USA
[6] Natl Inst Infect Dis Lazzaro Spallanzani IRCCS, HIV AIDS Dept, Rome, Italy
[7] Natl Inst Infect Dis Lazzaro Spallanzani IRCCS, Sci Direct, Rome, Italy
[8] Hosp Prato, Azienda USL Toscana Ctr, Dept Rheumatol, Prato, Italy
关键词
Baricitinib; SARS-CoV-2; COVID-19; IGRA; Specific immune-response; RESPONSES; CELLS;
D O I
10.1016/j.jinf.2021.02.023
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objective: Baricitinib seems a promising therapy for COVID-19. To fully-investigate its effects, we in-vitro evaluated the impact of baricitinib on the SARS-CoV-2-specific-response using the whole-blood platform. Methods: We evaluated baricitinib effect on the IFN-gamma-release and on a panel of soluble factors by multiplex-technology after stimulating whole-blood from 39 COVID-19 patients with SARS-CoV-2 antigens. Staphylococcal Enterotoxin B (SEB) antigen was used as a positive control. Results: In-vitro exogenous addition of baricitinib significantly decreased IFN-gamma response to spike- (median: 0.21, IQR: 0.01-1; spike+baricitinib 1000 nM median: 0.05, IQR: 0-0.18; p < 0.0001) and to the remainder-antigens (median: 0.08 IQR: 0-0.55; remainder-antigens+ baricitinib 100 0 nM median: 0.03, IQR: 0-0.14; p = 0.0013). Moreover, baricitinib significantly decreased SEB-induced response (median: 12.52, IQR: 9.7-15.2; SEB+ baricitinib 1000 nM median: 8, IQR: 1.44-12.16; p < 0.0 001). Baricitinib did modulate other soluble factors besides IFN-gamma, significantly decreasing the spike-specific-response mediated by IL-17, IL-1 beta, IL-6, TNF-alpha, IL-4, IL-13, IL-1ra, IL-10, GM-CSF, FGF, IP-10, MCP-1, MIP-1 beta(p <= 0.0156). The baricitinib-decreased SARS-CoV-2-specific-response was observed mainly in mild/moderate COVID-19 and in those with lymphocyte count >1 x 10(3)/mu l. Conclusions: Exogenous addition of baricitinib decreases the in-vitro SARS-CoV-2-specific response in COVID-19 patients using a whole-blood platform. These results are the first to show the effects of this therapy on the immune-specific viral response. (C) 2021 The Authors. Published by Elsevier Ltd on behalf of The British Infection Association.
引用
收藏
页码:58 / 66
页数:9
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