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      Effect of Biophysical Properties of Phosphatidylserine Particle on Immune Tolerance Induction Toward Factor VIII in a Hemophilia A Mouse Model.

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          Abstract

          A major complication in the replacement therapy of Factor VIII (FVIII) for Hemophilia A is the development of unwanted immune responses. Previous studies from our laboratory have shown that pretreatment of FVIII in the presence of phosphatidylserine (PS) resulted in hyporesponsiveness to subsequent administration of FVIII alone, due to the ability of PS to convert an immunogen to a tolerogen. We investigated the importance of biophysical properties of PS liposomes on its ability to convert an immunogen to a tolerogen. PS particles were prepared differing in size, protein-lipid topology, lamellarity, and % association to FVIII keeping the composition of the particle same. PS particles were prepared in 2 different sizes with differing biophysical properties: smaller particles in the nanometer range (200 nm) and larger size particles in the micron range (2 μm). Hemophilia A animals treated with both the nanometer and micron size PS particles showed a significant reduction in anti-FVIII antibody titers when compared to animals receiving free FVIII alone. Upon rechallenge with free FVIII animals that received FVIII along with the nanometer size particle continued to show reduced antibody responses. Animals receiving the micron size particle showed a slight increase in titers although they remained significantly lower than the free FVIII treated group. Upon culture with bone marrow derived dendritic cells, the nanometer size particle showed a reduction in CD40 expression and an increase in transforming growth factor-β cytokine production, which was not observed with the micron size particle. These results show that biophysical properties of PS play an important role in tolerance.

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          Author and article information

          Journal
          J Pharm Sci
          Journal of pharmaceutical sciences
          Elsevier BV
          1520-6017
          0022-3549
          October 2016
          : 105
          : 10
          Affiliations
          [1 ] Department of Pharmaceutical Sciences, University at Buffalo, The State University of New York, Buffalo, New York 14215.
          [2 ] Department of Pharmaceutical Sciences, University at Buffalo, The State University of New York, Buffalo, New York 14215. Electronic address: svb@buffalo.edu.
          Article
          S0022-3549(16)41503-0 NIHMS797036
          10.1016/j.xphs.2016.06.008
          5021571
          27431011
          5ad20f1f-6e70-4300-b9b6-d0ec09219cef
          History

          protein delivery,lipids,immune tolerance,phosphatidylserine,immunology

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