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Safety profile of high molecular weight polymerized hemoglobins.

Authors :
Muller CR
Williams AT
Munoz CJ
Eaker AM
Breton AN
Palmer AF
Cabrales P
Source :
Transfusion [Transfusion] 2021 Jan; Vol. 61 (1), pp. 212-224. Date of Electronic Publication: 2020 Oct 26.
Publication Year :
2021

Abstract

Background: Hemoglobin (Hb)-based oxygen (O <subscript>2</subscript> ) carriers (HBOCs) are being developed as alternatives to red blood cells and blood when these products are unavailable. Clinical trials of previous HBOC generations revealed side effects, including hypertension and vasoconstriction, that were not observed in preclinical studies. Large molecular weight (MW) polymerized bovine Hb (PolybHb) represents a new class of HBOC with promising results. We evaluated the safety profile of PolybHb after an exchange transfusion (ET) in guinea pigs (GPs). This study compares changes in indices of cardiac, inflammatory, and organ function after ET with high (R-state) and low (T-state) O <subscript>2</subscript> affinity PolybHb with high MW.<br />Study Design and Methods: Guinea pigs underwent a 20% ET with PolybHb. To assess the implication of PolybHb ET on the microcirculation, hamsters instrumented with a dorsal window chamber were subjected to a similar volume ET.<br />Results: T and R-state PolybHb did not induce significant alterations in cardiac function. T-state PolybHb induced mild vasoconstriction shortly after transfusion, while R-state did not have acute effects on microvascular tone.<br />Conclusion: Large MW PolybHbs were found to be safe and efficacious in increasing O <subscript>2</subscript> carrying capacity and the O <subscript>2</subscript> affinity of the PolybHb did not affect O <subscript>2</subscript> delivery or extraction by tissues in relevant preclinical models. In conclusion, these results suggest that both T-state and R-state PolybHb are safe and do not impair O <subscript>2</subscript> delivery. The results are encouraging and support further evaluation of high MW PolybHbs and their future feasibility compared to allogenic blood in a trauma model.<br /> (© 2020 AABB.)

Details

Language :
English
ISSN :
1537-2995
Volume :
61
Issue :
1
Database :
MEDLINE
Journal :
Transfusion
Publication Type :
Academic Journal
Accession number :
33104250
Full Text :
https://doi.org/10.1111/trf.16157