TY - JOUR
T1 - Immunomodulatory effects of plasma products on monocyte function in vitro
AU - investigators of the PALISI BloodNet network
AU - Shah, Sanjna
AU - Coppolino, Katirina
AU - Menocha, Somaang
AU - Beceiro, Susana
AU - Nateri, Jyotsna
AU - Spinella, Philip C.
AU - Nicol, Kathleen
AU - Hall, Mark W.
AU - Muszynski, Jennifer A.
N1 - Funding Information:
P.C.S. is a consultant for Octapharma, Cerus, and Entegrion. M.W.H. is on the Scientific Advisory Board of Bristol Meyers Squibb. The other authors declare no potential financial conflicts of interest. This work was supported by the Department of the Navy, Office of Naval Research (to J.A.M.). Spray-dried SD plasma products were supplied by Entegrion. Solvent/detergent plasma products were supplied by Octapharma. J.A.M. is supported by K08HL123925 and The Research Institute at Nationwide Children's Hospital. The aforementioned funders and suppliers played no role in study design, data analysis, manuscript preparation, or decision to publish.
Publisher Copyright:
© 2018 Lippincott Williams and Wilkins. All rights reserved.
PY - 2018/6/1
Y1 - 2018/6/1
N2 - BACKGROUND: Restoration of a balanced innate immune response is paramount to recovery from critical injury. Plasma transfusion may modulate innate immune responses; however, little is known about the immunomodulatory potential of various plasma products. We conducted in vitro experiments to determine the effects of fresh frozen plasma, thawed plasma, solvent/detergent plasma, and an investigational spray-dried solvent/detergent plasma product on monocyte function. METHODS: Monocytes were isolated from healthy adult volunteers and cocultured with aliquots of autologous plasma (control), fresh frozen plasma, thawed plasma, solvent/detergent treated plasma, or spray-dried solvent/detergent plasma. Monocyte function was assessed by cytokine production with and without lipopolysaccharide (LPS) stimulation, and flow cytometric assessment of HLA-DR cell surface expression. RESULTS: Monocyte cytokine production was not significantly altered after exposure to fresh frozen plasma or thawed plasma. In the absence of LPS, spray-dried solvent/detergent plasma exposure resulted in markedly increased IL-8 production compared to other plasma groups and controls (p = 0.01, analysis of variance [ANOVA]). Likewise, spray-dried SD plasma exposure resulted in higher LPS-induced IL-8, TNFα, and IL-1β production compared with autologous plasma controls (p < 0.0001; p < 0.0001, p = 0.002, respectively; ANOVA). LPS-induced IL-8 and TNFα production was lowest after exposure to solvent/detergent plasma (p < 0.0001, ANOVA). CONCLUSION: Exposure to spray-dried solvent/detergent plasma resulted in marked augmentation of monocyte inflammatory cytokine production. Solvent/ detergent plasma exposure resulted in the lowest cytokine production, suggesting lower immunomodulatory potential. Further work is needed to determine how these in vitro findings may translate to the bedside.
AB - BACKGROUND: Restoration of a balanced innate immune response is paramount to recovery from critical injury. Plasma transfusion may modulate innate immune responses; however, little is known about the immunomodulatory potential of various plasma products. We conducted in vitro experiments to determine the effects of fresh frozen plasma, thawed plasma, solvent/detergent plasma, and an investigational spray-dried solvent/detergent plasma product on monocyte function. METHODS: Monocytes were isolated from healthy adult volunteers and cocultured with aliquots of autologous plasma (control), fresh frozen plasma, thawed plasma, solvent/detergent treated plasma, or spray-dried solvent/detergent plasma. Monocyte function was assessed by cytokine production with and without lipopolysaccharide (LPS) stimulation, and flow cytometric assessment of HLA-DR cell surface expression. RESULTS: Monocyte cytokine production was not significantly altered after exposure to fresh frozen plasma or thawed plasma. In the absence of LPS, spray-dried solvent/detergent plasma exposure resulted in markedly increased IL-8 production compared to other plasma groups and controls (p = 0.01, analysis of variance [ANOVA]). Likewise, spray-dried SD plasma exposure resulted in higher LPS-induced IL-8, TNFα, and IL-1β production compared with autologous plasma controls (p < 0.0001; p < 0.0001, p = 0.002, respectively; ANOVA). LPS-induced IL-8 and TNFα production was lowest after exposure to solvent/detergent plasma (p < 0.0001, ANOVA). CONCLUSION: Exposure to spray-dried solvent/detergent plasma resulted in marked augmentation of monocyte inflammatory cytokine production. Solvent/ detergent plasma exposure resulted in the lowest cytokine production, suggesting lower immunomodulatory potential. Further work is needed to determine how these in vitro findings may translate to the bedside.
KW - Immune
KW - Monocyte
KW - Plasma
KW - Transfusion
KW - Trauma
UR - http://www.scopus.com/inward/record.url?scp=85053566839&partnerID=8YFLogxK
U2 - 10.1097/TA.0000000000001820
DO - 10.1097/TA.0000000000001820
M3 - Article
C2 - 29401191
AN - SCOPUS:85053566839
SN - 2163-0755
VL - 84
SP - S47-S53
JO - Journal of Trauma and Acute Care Surgery
JF - Journal of Trauma and Acute Care Surgery
IS - 6S
ER -