With the aim of reducing the damage to platelets while effectively rem
oving class I HLA antigens from their surfaces, we developed a new met
hod using acidified chloroquine diphosphate. Platelets were treated wi
th a 0.2 M solution of chloroquine diphosphate (pH 4.0). More than 90%
of the platelets remained viable after treatment. While a marked redu
ction in reactions of acidified chloroquine-treated platelets with mul
tispecific HLA antisera was noted in comparison with phosphate-buffere
d-saline-(PBS)-treated platelets, reactions with platelet-specific ant
ibodies were preserved. This was demonstrated by immunofluorescence te
sts and solid-phase and monoclonal antibody immobilization of platelet
antigen assays. Aggregation responses, though reduced in comparison w
ith PBS-treated platelets, were still preserved after acidified chloro
quine treatment. Ultrastructural analysis did not show any significant
difference from PBS-treated platelets. We conclude that treatment of
platelets with acidified chloroquine diphosphate is a simple and effec
tive method for removing class I HLA antigens from their surfaces with
minimal damage to their structure and function.