The low antigenicity of the GPA is due to its preparation with glycerol, which removes the vital components of the cell and renders the cell non viable.[1, 8] A previous study has shown that the rejection of GPA is due to the inflammatory processes that is most probably mediated by host monocyte infiltration rather than by a rejection process mediated by T-cells.[9] Meanwhile, GPA has been demonstrated to have a lower risk of transmissible disease, even with HIV due to its preservation process. Here, GYPA is linked to infectious disease.